105 Jobs für Clinical Trials Director
Stellenangebote Clinical Trials Director Jobs
Job vor 10 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
• Frankfurt
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ] Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. [. .. ]
Job vor 10 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Hamburg, HH
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ] Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. [. .. ]
Job vor 10 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Düsseldorf, NW
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ] Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. [. .. ]
Job vor 10 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Cologne, NW
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ] Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. [. .. ]
Job vor 10 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Leipzig, SN
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ] Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. [. .. ]
Job vor 10 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Dortmund, NW
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ] Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. [. .. ]
Job vor 11 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Essen, NW
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ] Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. [. .. ]
Job vor 11 Tagen bei Mindmatch.ai gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Stuttgart, BW
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ] Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. [. .. ]
Job vor 11 Tagen bei Neuvoo.com gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ] Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. [. .. ]
Job vor 11 Tagen bei Neuvoo.com gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
• Bavaria Munich
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key internal stake holders throughout the life cycle of the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication [. .. ] Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. [. .. ]
Job vor 4 Tagen bei Stellen-Online.de gefunden
BioNTech
• Mainz, 55116
Führungs-/ Leitungspositionen
[. .. ] supporting the oncology therapeutic area by providing medical safety expertise to one or more study management teams. In collaboration with assigned Safety Scientists, the MSP ensures patient [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] safety throughout the clinical trial process. Responsibilities include contributing to clinical trial protocols, training investigators, assessing safety data (e. g. , adverse events of special interest and serious adverse events) , determining necessary follow-up actions, and conducting safety signal detection and evaluation. The MSP also ensures compliance with Good Clinical Practice (GCP) and [. .. ] on development strategies for innovative oncology products, particularly those of USHas achieved demonstrable results in a matrix organization and in a multidisciplinary team, experience in implementing GCP standards in clinical trials, in particular safety reporting in compliance with global and local regulations Your benefits and remuneration:Compensation for the role will depend on several factors, including responsibilities of the job, education, experience, knowledge, skills, and abilities. Compensation at other locations may vary significantly. Bio NTech is committed to the wellbeing of our team [. .. ]
Job am 22.08.2026 bei Stellen-Online.de gefunden
BioNTech
Director CTSM, Supply Data Integration-Vollzeit
• Mainz, 55116
Führungs-/ Leitungspositionen
Jobticket
London, United Kingdom; Mainz, Germany; Munich, Germany full time Job ID: 11624 About the Role:As
Director CTSM Supply Data Integration, you will lead the deployment, configuration, and optimization of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Bio NTechs Intelligent Clinical Supply Management (ICSM) SAP module within our global Clinical Trial Supply Management (CTSM) division. Acting as a strategic counterpart to IT, you will ensure seamless data flow, accuracy of information, and optimized processes across clinical trials and external partners. In this pivotal leadership role, you will collaborate with cross-functional stakeholders to drive innovation in clinical supply chain management. Your expertise will directly contribute to advancing Bio NTechs mission of delivering transformative therapies while setting new standards in clinical trial supply management. Your Contribution:Act as Business Process [. .. ]
Job am 22.08.2026 bei Stellen-Online.de gefunden
Ideals
• Deutschland, 99986
Führungs-/ Leitungspositionen
[. .. ] and make important decisions with less stress, higher quality, and shorter hours. Ideals Virtual Data Room (VDR) : Secure document sharing and collaboration for due diligence, fundraising, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] corporate reporting, licensing, clinical trials, and other complex transactions. Ideals Board: Board and leadership collaboration platform for faster, safer, and more compliant decision-making. The role Ideals has grown 2x in the past four years to a team of 500+ people across 30+ countries. The next stage is more ambitious: scaling toward unicorn status, with significant hiring volume concentrated in GTM teams across the EMEA, Americas, and APAC. To get there, we need a Director of Talent Acquisition who operates at both levels. Strategically, you ll report directly to the CEO and shape how TA supports revenue growth aligning hiring priorities with business targets, driving adoption of AI and automation, and holding quality of hire as a non-negotiable. Tactically, you ll lead a team [. .. ]
Job am 22.08.2026 bei Stellen-Online.de gefunden
Precision Medicine Group
Director, CDx Regulatory Consultant-Vollzeit
• Deutschland, 99986
Führungs-/ Leitungspositionen Beratungs-/ Consultingtätigkeiten
Position Summary:The
Director, CDx Regulatory Consultant will be responsible for applying deep expertise in companion diagnostic regulatory strategy, IVD development, quality system expectations, and global marketing authorization pathways to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] advise pharmaceutical, biotechnology, and diagnostic clients on the development, clinical trial use, approval, and lifecycle management of companion diagnostics. This role will translate complex FDA, EU IVDR, and other global regulatory requirements into practical, actionable strategies that support Rx Dx co-development, patient selection assays, analytical and clinical validation planning, clinical trial enabling submissions, and coordinated diagnostic and therapeutic commercialization. [. .. ] diagnostic development, biomarker strategy, clinical trial enrollment, therapeutic development milestones, and commercialization objectives for pharmaceutical, biotechnology, and diagnostic clients. Advise clients on regulatory requirements for use of assays in clinical trials, including patient selection, inclusion or exclusion testing, significant risk and nonsignificant risk determinations, IRB considerations, investigational device requirements, and global performance study obligations. Direct the preparation of global regulatory submissions and supporting documentation for companion diagnostics and clinical trial assays, including FDA Q-Submissions, Pre-IDE packages, IDEs, PMAs, PMA [. .. ]
Job am 22.08.2026 bei Stellen-Online.de gefunden
Bio Marin Pharmaceutical
• Deutschland, 99986
Führungs-/ Leitungspositionen
[. .. ] who manage our technology to the human resources professionals who hire the people who make it all possible, these teams support our organization and span all areas [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of operations. Associate Director, Corporate Compliance Location: Frankfurt ( Hybrid role) Closing Date: 14 August 2026Summary Description The Associate Director, Corporate Compliance serves as the Country Compliance Officer for Germany and is the primary compliance business partner to the German leadership team. The role is responsible for overseeing the implementation and effectiveness of Bio [. .. ] business policies and German law to ensure continuing relevance in providing guidance to management and employees; Collaborate with other company functions, including, but not limited to Commercial Operations, Medical Affairs, Clinical Sciences and Regulatory Affairs to provide advice and counsel regarding potential compliance issues and risks; Draft memoranda providing analysis and risk-based recommendations regarding various compliance rules and regulations implicated by proposed or existing business strategies; Evaluate, approve, and monitor company interactions with healthcare professionals, healthcare organisations, patient organisations and [. .. ] policies; Review of communications related to the companys development programmes to ensure they accurately and appropriately inform interested parties as to relevant information about the status and progress of clinical trials; Maintain an effective and proactive compliance communication and training programme in Germany (through Learning Management System and Live trainings) , including promoting use of the compliance hotline and expeditiously and thoroughly fielding questions relating to new and existing compliance issues and related policies and procedures raised by management and employees; [. .. ]
Job vor 3 Tagen bei Mindmatch.ai gefunden
IQVIA
Principal, Regulatory Science and Strategy-Real World Solutions
• AT- 9 Wien
[. .. ] purposes. RSS sells and delivers as a unified team, partnering with clients on regulatory strategy, study design, and submission planning across drugs, biologics, and devices. Our work [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] spans externally controlled trials, post-marketing requirements (PMRs/ PMCs) , post-authorization safety studies (PASS) , drug utilization studies (DUS) , and emerging regulatory technology. We are strategic thinkers, deep subject matter experts, and creative at our core. We are collaborative, intellectually curious, and entrepreneurial. About the role: As a Principal (Director-level) within RSS, you will own delivery leadership, drive business development, and serve as a subject matter expert across two connected areas: selling and delivering standalone regulatory strategy engagements and cross-functional RWE studies for regulatory decision-making. Your work will focus primarily on several areas: First, a Principal is [. .. ] efforts. Identify follow-on work and new revenue opportunities with existing clients, and support business development efforts with new client organizations. Collaborate across IQVIA when client requirements span regulatory affairs, clinical development, and real world insights. Provide direction, advice, and intellectual leadership to delivery teams and clients. Contribute high-level input to client reports and presentations, and deliver findings to clients directly. Mentor and coach junior consultants, sharing subject matter expertise to build RSS capability. Participate in annual performance review processes [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
[. .. ] purposes. RSS sells and delivers as a unified team, partnering with clients on regulatory strategy, study design, and submission planning across drugs, biologics, and devices. Our work [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] spans externally controlled trials, post-marketing requirements (PMRs/ PMCs) , post-authorization safety studies (PASS) , drug utilization studies (DUS) , and emerging regulatory technology. We are strategic thinkers, deep subject matter experts, and creative at our core. We are collaborative, intellectually curious, and entrepreneurial. About the role: As a Principal (Director-level) within RSS, you will own delivery leadership, drive business development, and serve as a subject matter expert across two connected areas: selling and delivering standalone regulatory strategy engagements and cross-functional RWE studies for regulatory decision-making. Your work will focus primarily on several areas: First, a Principal is [. .. ] efforts. Identify follow-on work and new revenue opportunities with existing clients, and support business development efforts with new client organizations. Collaborate across IQVIA when client requirements span regulatory affairs, clinical development, and real world insights. Provide direction, advice, and intellectual leadership to delivery teams and clients. Contribute high-level input to client reports and presentations, and deliver findings to clients directly. Mentor and coach junior consultants, sharing subject matter expertise to build RSS capability. Participate in annual performance review processes [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
Bridge Bio Pharma
Director, Patient Advocacy, International
• AT- 2 Lavamünd
Führungs-/ Leitungspositionen
[. .. ] diseases and genetically defined cancers. Since our founding in 2015, we have built a diverse portfolio of more than 20 drug development programs, ranging from early discovery [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to late-stage clinical trials, across multiple therapeutic areas including precision oncology, cardiology, endocrinology, neurology, and renal disease. We have already achieved regulatory approval for three therapies and continue to advance promising science from academia into meaningful treatments for patients worldwide. Who We Are Bridge Bio is a global biotechnology company with our Global Headquarters [. .. ] a meaningful impact for patients. Our people are trusted and empowered, united by urgency, purpose, and the drive to advance science for patients around the world. What Youll Do The Director, Patient Advocacy, for Hypoparathyroidism leads the development and execution of Calcilytixs patient advocacy strategy in support of clinical development and commercialization, while safeguarding long-term patient trust and community relationships. Reporting to the Senior Director of Global Patient Advocacy for Calcilytix, this role drives engagement across the International Hypoparathyroidism community, [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
CSL Plasma Inc.
• AT- 2 Lavamünd
Führungs-/ Leitungspositionen
Position Purpose The Associate
Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] obligations. The individual will work closely with the Director, Statistical Programming to ensure all assigned Statistical Programming tasks are managed to completion. Work closely with Statisticians [. .. ] ensure high quality, timely, delivery of assigned projects. Ensure realistic project planning. Oversee the CRO delivery or manage the in-house programming of data sets, outputs, and DDT files of clinical trials and integrated analysis. Plans and leads the design and implementation of complex specifications and programs for applications designed to analyze and report complex clinical trial data in CDISC format. Coordinating the oversight or in-house programming of exploratory analyses, analyses to support secondary publications, response to regulatory requests, or other [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
Novocure Inc.
Clinical Trial Physician, Oncology
• AT- 2 Schweiz
Select how often (in days) to receive an alert: Create Alert CH Wayne, PA, US, 19087 Portsmouth, NH, US, 03801 As our new
Clinical Trial Physician, Oncology, youll play [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a key part in this mission. As a key member of our multi-disciplinary oncology team, you will serve as a medical expert supporting Tumor Treating Fields (TT Fields) Therapy clinical programs. Depending on experience and level, you will either lead a clinical study or [. .. ] a clinical study while contributing to the broader medical strategy ABOUT YOU Medical Degree At least 5 years of clinical research experience working within pharmaceutical, biotech, or medical device companies (Director level) At least 10 years of clinical research experience working within pharmaceutical, biotech, or medical device companies (Senior Director level) Demonstrated experience leading global clinical trials or overseeing international clinical study programs across multiple regions Previous experience leading physician teams and managing direct reports (Senior Director level) Strong understanding of the clinical development process, including matrix multidisciplinary teams, regulatory submissions, and data analysis Sound understanding in oncology clinical research, with tumor-based program experience Hands-on [. .. ]
Job am 07.08.2026 bei Mindmatch.ai gefunden
Biogen, Inc.
Associate Director, Country Site Operations FSP Oversight Manager
• AT- 2 Schweiz
Führungs-/ Leitungspositionen
Associate
Director, Country Site Operations FSP Oversight Manager Applyremote type: Hybridlocations: Baar, Switzerlandtime type: Full timeposted on: Posted Todayjob requisition id: REQ23832For our offices in Baar we are recruiting [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] for a Associate Director, Country Site Operations FSP Oversight Manager About This Role: As the Associate Director, Country Site Operations Functional Service Provider [. .. ] leadership and cross-functional stakeholders to drive and manage the CSOs FSP insourcing model. This role is crucial in overseeing and developing FSP staff who support country-and site-facing clinical trial execution, ensuring the embedding of consistent, efficient processes across regions and therapeutic areas. Your work will ensure alignment with CSOs internal and external stakeholders on FSP role execution, performance, quality, and delivery expectations. Additionally, you will contribute to shaping CSO operational strategy and continuous improvement as part of the CSO extended leadership model. Through varied responsibilities, you will have the opportunity to impact the execution of clinical trials and support the broader strategic goals of the business. What Youll Do: Manage up to 20-25 FSP staff assigned across the clinical portfolio to support CSOs country-and site-level operational objectives. Lead resource forecasting, assignment, and prioritization to support regional delivery needs, portfolio demand, and annual operating plan [. .. ]
Neu Job vor 2 Std. bei Jobleads gefunden
Senior Director, Legal Compliance, OUS Regions
Führungs-/ Leitungspositionen
# Senior
Director, Legal Compliance, OUS Regions Corcepttherapeutics On-site Bavaria Corporate Functions Posted Sep 9, 2026For more than 25 years, Corcept has been singularly focused on the science of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1, 000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit Reporting to the VP, Legal Compliance, the Senior Director, [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Senior Director, Legal Compliance, OUS Regions
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1, 000 proprietary selective cortisol modulators and glucocorticoid receptor [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, Reporting to the VP, Legal Compliance, the Senior Director, Legal Compliance, OUS Regions will serve as lead legal counsel for Corcepts burgeoning operations outside the United States, with particular focus on the European Economic Area, Switzerland and the United Kingdom. This role will provide legal and compliance guidance for a broad scope of legal issues and clients in support [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Director, Medical Affairs DACH
• Hamburg
Führungs-/ Leitungspositionen
[. .. ] Job Function Medical Affairs Group Job Sub Function Medical Affairs MD Job Category People Leader All Job Posting Locations Hamburg, Germany Job Description De Puy Synthes is [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] recruiting for a Director, Medical Affairs DACH, located in Hamburg, Germany The Country Medical Lead is a member of the Country DPS Board, functioning as a strategic collaborator, bringing surgical insights, knowledge of local healthcare ecosystems, policy, trends and guidelines to inform and support shaping the commercial strategy, maximizing opportunities DPS Country business. This [. .. ] to the DS MA Lead International with a dotted line to the Country Depuy Synthes Managing Director. Tasks/ Duties/ Responsibilities Supports Country business leaders by Understanding needs of the different clinical and non-clinical stakeholders in the healthcare environment and building strong relationships externally with key stakeholders (Strategic Accounts, Hospital Groups, Regulatory Agencies, Medical Societies, etc. ) to drive business initiatives building strong relationships and partnerships with customers, especially focused on the development of Key Opinion Leaders. anticipating, evaluating and responding [. .. ] us via https:/ / internal employees contact Ask GS to be directed to your accommodation resource. #De Puy Synthes Careers Required Skills Preferred Skills Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Consulting, Developing Others, Healthcare Trends, Inclusive Leadership, Leadership, Medical Affairs, Medical Communications, Medical Compliance, Product Strategies, Representing, Research Proposals, Stakeholder Management, Strategic Thinking The Anticipated Base Pay Range For This Position Is 119, 200.00-205, 620.00 Benefits In addition to base pay, we offer the following [. .. ]
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Director/ Senior Director FSP Operational Delivery Lead-EMEA
Führungs-/ Leitungspositionen
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a
Director Project Management-Make an Impact at the Forefront of Innovation We have successfully supported the top [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 50 pharmaceutical companies and more than 750 biotechs, spanning 2, 700 clinical trials across 100+ countries in the last 5 years. The Director/ Senior Director, FSP Project Oversight provides enterprise-level leadership across multiple strategic FSP accounts, therapeutic areas, and global delivery organizations. This role is responsible for driving portfolio strategy, operational transformation, client partnership growth, and organizational performance while ensuring alignment with [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Director pro Jahr?
Als Clinical Trials Director verdient man zwischen EUR 80.000,- bis EUR 120.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Director Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 105 offene Stellenanzeigen für Clinical Trials Director Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Director Jobs?
Aktuell suchen 12 Unternehmen nach Bewerbern für Clinical Trials Director Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trials Director Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trials Director Stellenangebote:
- BioNTech (2 Jobs)
- Ideals (1 Job)
- Precision Medicine Group (1 Job)
- Bio Marin Pharmaceutical (1 Job)
- IQVIA (1 Job)
In welchen Bundesländern werden die meisten Clinical Trials Director Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Director Jobs werden derzeit in Rheinland-Pfalz (9 Jobs), Sachsen (8 Jobs) und Niedersachsen (7 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Director Jobs?
Clinical Trials Director Jobs gehören zum Berufsfeld Biotechnologie.
