125 Jobs für Clinical Trials Director
Stellenangebote Clinical Trials Director Jobs
Job vor 13 Tagen bei Jobleads gefunden
• Eschborn, Hessen
Führungs-/ Leitungspositionen
Director, Medical Affairs page is loaded # # Director, Medical Affairslocations: Germany-Hesse-Eschborntime type: Full timeposted on: Posted Todayjob requisition id: 31144421 # # JOB DESCRIPTION:Director Global Medical Affairs-Heart Failure Abbott [...]
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[...] Heart Failure Division Abbotts Heart Failure business is expanding its Global Medical Affairs organization, and we are seeking [. .. ] Role Matters This is a highimpact position at the forefront of advancing innovative therapies for patients living with heart failure. The Director will play a key role in guiding the clinical and scientific strategy across a rapidly evolving portfolio, partnering closely with Clinical Affairs, R D, Market Access, Marketing, and Commercial teams. The role requires a significant global presence (approx. 60 travel) to engage with investigators, clinical sites, and internal stakeholders. This position will manage Clinical Research professionals to provide medical [. .. ] and delivers internal educational activities related to HF Provide input to R D on all aspects and stages of the product portfolio Support clinical affairs and help drive Abbott led trials and ensure the region is represented in critical evidence generation in the field of HF. Be responsible for off label discussions with clinicians in the OUS region. Assist market access with clinical input to reimbursement processes OUS Represent Abbott HF Medical Affairs in interactions with regulatory bodies Assists investigation teams [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Medical Director
• Zürich
Führungs-/ Leitungspositionen
Discover Intenarnational is partnered with a Swiss Biotech in their search for an experienced Medical
Director Oncology to provide medical and
clinical leadership across a portfolio of innovative oncology assets [...]
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[...] within a fast-growing biotech group. This role will lead oncology clinical development strategy, provide medical oversight across studies, and work closely with R D and executive leadership to advance novel cancer therapies through clinical development. Key Responsibilities Lead medical strategy for [. .. ] leadership to internal teams, KOLs, and external partners Contribute to portfolio assessment and oncology asset strategy Requirements Md/MBBS with significant oncology drug development experience Strong background in clinical oncology trials (Phase IIII) Experience in biotech or pharma clinical development Excellent knowledge of GCP and oncology regulatory requirements Strong leadership and stakeholder management skills #J-18808-Ljbffr 88847617 [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
The Medical
Director will support
clinical trials across early to late development phases, contributing to clinical strategy, safety oversight, and data interpretation. This role involves collaboration across crossfunctional teams to [...]
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[...] deliver on clinical development goals and regulatory milestones. This is a Hybrid position. Key Responsibilities Draft and review clinical trial documents (protocols, IBs, ICFs, CSRs) . Serve [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Therapeutic Area Medical Director
• München, Bayern
Führungs-/ Leitungspositionen
We are seeking several Medical Directors to join our dynamic team. The Medical
Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, [...]
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[...] and reporting of clinical trials. This role acts as the Medpace internal medical expert and serves as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
A leading biopharmaceutical company is seeking a Medical
Director in Basel, Switzerland to support
clinical trials across early to late development phases. This role involves drafting clinical trial documents, serving [...]
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[...] as a medical monitor, and overseeing safety data. Candidates should possess a medical degree and at least 5 years of experience in clinical research, including 3 years in oncology. The position is hybrid, enabling collaborative work [. .. ]
Job am 30.03.2026 bei Jobleads gefunden
Global Medical Director, Autoimmune Trials Remote
Führungs-/ Leitungspositionen
A leading global pharmaceutical company is seeking a Medical
Director to join their
Clinical Development team in Switzerland. The role involves overseeing clinical
trials, ensuring patient safety, and collaborating [...]
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[...] with regulatory bodies. The ideal candidate will have a Medical Degree, a minimum of 3 years in clinical research, and proven leadership skills in the field of autoimmune diseases. This position offers a permanent, full-time contract with a remote work option. #J-18808-[. .. ]
Job am 29.03.2026 bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] Diseases represent a major focus area where we are committed to realizing our long-term vision of changing lives of patients with severe brain disorders. Our preclinical research [...]
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[...] and early clinical development activities center around large and rare indications. With unparalleled strengths across diverse disciplines, Roche is uniquely positioned to lead in transforming science into medicines for patients with disorders of the nervous system. To achieve our goals, we are seeking a Medical Director, focusing on multiple sclerosis. The Opportunity In this role, you will lead and/or support early-stage clinical projects from entry into a human through proof of mechanism and proof of concept, to transform molecules into new medicines in an area with huge unmet medical needs. You will leverage your [. .. ] external engagements with advisory boards, site investigators, health authorities, and other key stakeholders Provide clinical input to programs in discovery research Lead scientific communications and disseminate the results of clinical trials in the form of conference presentations and journal publications Who You Are You have an MD or Md/Ph D with a speciality in neuroimmunology, multiple sclerosis, or a similar field. Board certification and fellowship training or research experience in relevant areas is preferred You bring at least 5 years of [. .. ]
Job am 23.03.2026 bei Jobleads gefunden
Director, Medical Affairs
• Freiburg im Breisgau, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] technologies fuels active lifestyles in orthopedics and beyond. For more information about Enovis, please visit Was Sie tun werden What Youll Do Oversees the direction, planning, execution [...]
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[...] and interpretation of clinical trials/ research and data collection activities along with regulatory compliance, patient safety and emerging patient risks. May establish and approve scientific methods for design and implementation of clinical protocols, data collection systems and final reports. Provides input on clinical study design, execution, and data analysis. Leads the adverse event reporting and [. .. ]
Job am 21.03.2026 bei Jobleads gefunden
• Gräfelfing, Bayern
Führungs-/ Leitungspositionen
Your mission We are looking for an experienced and strategic Medical
Director (m/f/x) to provide medical leadership for a mature global Phase 3 program in relapsing Multiple Sclerosis. In [...]
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[...] this role, you will combine deep strategic understanding of MS clinical outcomes with handson medical monitoring expertise to support the successful execution of a registrational study, evaluating safety and efficacy. Clinical Strategy Leadership: Lead the unblinding, data review, and readout of two Phase 3 clinical trials in relapsing MS, including comprehensive data analysis and interpretation. Provide medical leadership for Clinical Study Reports. Regulatory Interactions: Support and participate in pre NDA regulatory activities (FDA, EMA) , ensuring clear communication of clinical outcomes and study rationale. Scientific Expertise External Engagement: Collaborate closely with the medical advisory board and key [. .. ]
Job am 01.03.2026 bei Jobleads gefunden
Medical Director Safety
• Lausanne, Waadt
Führungs-/ Leitungspositionen
[. .. ] core. A dynamic international environment empowering you to learn, develop and grow. Dont hesitate to connect with us during the recruitment process to learn more Position Summary [...]
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[...] As a Medical Director for Clinical Trial/ Research Safety you will provide expert safety leadership and input to clinical development programs for nutritional solutions and therapeutics across the lifespan, and ensure safety compliance with regulatory frameworks applicable to pharma, medical nutrition and food for medical purposes (FSMP) . A Day in the Life of a Medical [. .. ] years experience in clinical research and safety, in development or operations (pharma, biotech, diagnostics, medtech, nutrition, or CRO settings) Experience and proven impact in leading safety management in complex clinical trials, including issue management and regulatory frameworks of nutrition and medical nutrition Expertise in preparation of clinical safety assessments and regulatory submissions involving safety information Strong strategic acumen with experience in collaborating across matrixed, cross-functional teams Ability to analyze, interpret, and communicate complex clinical and scientific information Effective external engagement [. .. ]
Job am 24.02.2026 bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Overview The IQVIA Cell and Gene Therapy Center of Excellence (CAGT COE) , a hub of CAGT
clinical innovation, is growing We are looking for an exceptional Board-Certified physician [...]
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[...] to join our team as a Medical Strategy Lead to help us expand our CAGT portfolio, with an emphasis on Gene Therapy/ Gene Editing platforms, and advance this dynamic and rapidly expanding area of clinical development. The CAGT Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical trials in CAGT and especially in the areas of Gene Therapy/ Gene Editing, who will be a champion for CAGT across IQVIA. The key remit of the role is drive growth of the IQVIA CAGT portfolio through scientific and clinical expertise. The CAGT Medical Strategy Lead will be charged with using [. .. ]
Job am 21.02.2026 bei Jobleads gefunden
Senior Medical Director-Cell and Gene Therapy (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Senior Medical
Director-Cell and Gene Therapy (m/w/d) page is loaded # # Senior Medical Director-Cell and Gene Therapy (m/w/d) locations: Frankfurt, Hesse, Germanytime type: Full timeposted on: Posted Todayjob [...]
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[...] requisition id: R1529858Job Overview The IQVIA Cell and Gene Therapy Center of Excellence (CAGT COE) , a hub of CAGT clinical innovation, is growing We are looking for an exceptional Board-Certified physician to join our team as a Medical Strategy Lead to help us expand our CAGT portfolio, with an emphasis on Gene Therapy/ Gene Editing platforms, and advance this dynamic and rapidly expanding area of clinical development. The CAGT Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical trials in CAGT and especially in the areas of Gene Therapy/ Gene Editing, who will be a champion for CAGT across IQVIA. The key remit of the role is drive growth of the IQVIA CAGT portfolio through scientific and clinical expertise. The CAGT Medical Strategy Lead will be charged with using [. .. ]
Job am 15.02.2026 bei Jobleads gefunden
Medical Director
Führungs-/ Leitungspositionen
Overview EPM Scientific are currently partnered with a leading global pharmaceutical company focused on developing innovative therapies in autoimmune diseases. They are seeking a Medical
Director (Ad/Director Level) to [...]
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[...] join their Clinical Development team. See a short summary below: Contract Conditions Start date: As soon as possible (3 Month Notice taken into account) Location: Switzerland/Spain/ Poland-Remote Contract Type: Permanent, Full Time Key Responsibilities Lead the strategic design and execution of global clinical trials in autoimmune indications, ensuring alignment with regulatory standards and company goals. Act as medical monitor for clinical studies, overseeing patient safety, data integrity, and compliance with GCP. Collaborate cross-functionally with internal teams and external stakeholders including investigators, KOLs, and regulatory bodies across EU, US, and other regions. Provide scientific [. .. ]
Job am 22.01.2026 bei Jobleads gefunden
Head of Clinical Operations-ONCOLOGY-HYBRID
• München, Bayern
Führungs-/ Leitungspositionen
We are partnering with a growing, oncology-focused biotech to appoint a Head of
Clinical Operations at Senior
Director or VP level. This is a critical leadership role reporting [...]
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[...] directly to the Chief Medical Officer, based in Munich with a hybrid working model (3 days on site) . This position offers the opportunity to make a meaningful impact at a pivotal stage of the companys development. The organisation is currently running Phase II clinical trials and preparing to advance into Phase III, with a strong focus on solid tumours. The Role As Head of Clinical Operations, you will provide handson leadership across global clinical programmes, shaping and executing the clinical operations strategy while remaining close to day-to-day execution. Key responsibilities include: Leading, mentoring, [. .. ]
Job am 21.01.2026 bei Jobleads gefunden
• Kassel, Hessen
Führungs-/ Leitungspositionen
[. .. ] starting materials, coupled with specialty lab services. Key Responsibilities: Lead an international team of pathologists Maintain and grow our existing network in the global pathology community Act [...]
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[...] as a medical director for the Discovery site in Kassel, Germany. Optimize pathology related processes Guide/ assist our teams in assay development and validation which includes semiquantitative as well as quantitative assays Support/ consult our project management and business development team as well as our clients Evaluation of clinical trial specimens Act as a trainer for external pathologists within our post approval services for the interpretation/ scoring of novel biomarkers Preparation of publications/ posters in collaboration with our customers Position Qualifications (Education, Skills, Experience) : Board certification (German board certification preferred) Additional training in Cytology Experience in hematopathology and/[. .. ] knowledge in IHC, m IF, FISH, RNA in situ hybridization to support the assay development team as well as to act as an experienced reader and consultant for customers in clinical trials. Experience in digital imaging applications and the evaluation of biomarkers via digital image analysis software Teamplayer Willingness to work in a GCLP environment Compensation and Benefits: Discovery Life Sciences is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market [. .. ]
Job am 16.01.2026 bei Jobleads gefunden
Psychiatry-Medical Director
• München, Bayern
Führungs-/ Leitungspositionen
Join to apply for the Psychiatry-Medical
Director role at Medpace We are seeking a Psychiatry Medical Director to join our dynamic team. The Medical Director will have overall responsibility [...]
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[...] for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project [. .. ]
Job am 15.01.2026 bei Jobleads gefunden
Führungs-/ Leitungspositionen
Overview Senior/ Medical
Director (Ophthalmology) , 0.5 FTE. TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their [...]
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[...] clinical development journey. Join our team as a Senior/ Medical Director (Ophthalmology) . The Senior/ Medical Director is a key member of the Project Delivery team, working independently to manage safety and medical matters in line with company policies, standard operating procedures (SOPs) , and regulatory requirements. With deep medical expertise, [. .. ] Regulatory Risk Support: Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical Monitoring Signal Detection: Serve as a medical monitor in trials, perform literature reviews, and contribute to signal detection and interpretation. Regulatory Document Contributions: Offer expert medical insight into regulatory submissions and safety-related documentation. Team Client Engagement: Mentor junior medical staff, support SOP/ tool development, and join Commercial Operations in client meetings and presentations. Qualifications Medical Qualifications: Medical Doctor (MD) [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Neo Carbon
Director of Project Management (m/f/d)
• Regierungsbezirk Kassel; Hessen
Führungs-/ Leitungspositionen
[. .. ] can outpace their competition and push the leading edge of innovation using our Science at your Service TM business model. Position Summary: Discovery is looking for a [...]
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[...] talented and passionate Director of Project to harmonize project management teams within our Specialty Lab Services (SLS) teams, which includes IHC, Molecular Pathology, Genomics, Proteomics, and Flow Cytometry. As an individual contributor, the Director of Project Management for Specialty Lab Services plays a key role in overseeing clinical and scientific project management teams within the business, creating and harmonizing project management processes across laboratories, overseeing multiple business segments and multi-site projects, collaborating with stakeholders, and driving streamlined and successful project management across SLS. This position requires a deep understanding of the scientific capabilities within SLS and strong [. .. ] Project Management certification (PMI or similar) preferred. Minimum of 10 Years of experience in clinical trial services with pharma and biotech companies. This includes long-standing experience in prospective clinical trials and companion diagnostics performance studies using immunohistochemistry, genomics, proteomics, or flow cytometry methodologies Work experience in a regulated environment/ quality management system (e. g. GCLP) Excellent verbal and written communication and negotiation skills. Ability to collaborate and support teams working in different geographic locations Ability to create, lead, and maintain [. .. ]
Job vor 5 Tagen bei Jooble gefunden
Biontech
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
As Associate
Director Statistical Programming you will be responsible for representing Statistics in all assigned cross-functional
clinical study teams and other projects and holding accountability for all statistical [...]
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[...] aspects, as well as for providing statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables. Your main responsibilities are: Work as part of a collaborative, cross-functional team [. .. ] staff (internal as well as outsourced) and in representing Biostatistics in a matrix organization and in a multidisciplinary team Experiences in planning, conducting and analyses of oncology or infectious diseases trials from phase I-IV, including scientific publications Experience in answering health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ ISS packages Good knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a Plus) , regulatory guidelines [. .. ]
Job vor 5 Tagen bei Jooble gefunden
Biontech
(Senior) Director Biostatistics
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
As (Senior)
Director Biostatistics you will represent Statistics in all assigned cross-functional
clinical study teams and other projects and be accountable for all statistical aspects serving as the [...]
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[...] biostatistics lead core team member for all assigned programs. You will also be responsible for providing statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate [. .. ] staff (internal as well as outsourced) and in representing Biostatistics in a matrix organization and in a multidisciplinary team Experiences in planning, conducting and analyses of oncology or infectious diseases trials from phase I-IV, including scientific publications Experience in leading to health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ ISS packages Very good knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a Plus) , [. .. ]
Job vor 13 Tagen bei Jooble gefunden
Director, Medical Affairs (m/f/d)
• Landkreis Main- Taunus- Kreis; Regierungsbezirk Darmstadt; Hessen Eschborn, DE
Führungs-/ Leitungspositionen
Director Global Medical Affairs-Heart Failure (m/f/d) Abbott Heart Failure Division Abbotts Heart Failure business is expanding its Global Medical Affairs organization, and we are seeking an experienced Director, Global [...]
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[...] Medical Affairs to help shape the future of mechanical circulatory support and hemodynamic management worldwide. This strategic leadership role [. .. ] Role Matters This is a highimpact position at the forefront of advancing innovative therapies for patients living with heart failure. The Director will play a key role in guiding the clinical and scientific strategy across a rapidly evolving portfolio, partnering closely with Clinical Affairs, R D, Market Access, Marketing, and Commercial teams. The role requires a significant global presence (approx. 60 travel) to engage with investigators, clinical sites, and internal stakeholders. This position will manage Clinical Research professionals to provide medical [. .. ] and delivers internal educational activities related to HF Provide input to R D on all aspects and stages of the product portfolio Support clinical affairs and help drive Abbott led trials and ensure the region is represented in critical evidence generation in the field of HF. Be responsible for off label discussions with clinicians in the OUS region. Assist market access with clinical input to reimbursement processes OUS Represent Abbott HF Medical Affairs in interactions with regulatory bodies Assists investigation teams [. .. ]
Job am 13.04.2026 bei Jooble gefunden
dehaze GmbH
Medical Lead
• Berlin Berlin, DE
Führungs-/ Leitungspositionen
[. .. ] and make a call under uncertainty. At some point, you realized you could have more impact beyond direct patient and you started building a second dimension alongside [...]
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[...] or after your clinical work. dehaze AI identifies chronic disease risks on already existing health data. Thanks to us, our customers, fully integrated health insurers, save 10 of their yearly health budget. In an industry with relatively low margins, a real game changer. You are the medical authority inside dehaze. But this is not [. .. ] university hospitals and research groups to co-validate our approach and publish findings. Represent dehazes clinical credibility to customers: When we sit across from a chief medical officer or medical director at a health network, you convey the medical validity of our solution. You speak their language because youve been in their world. Shape the clinical roadmap: You advise our product team on medical requirements for prioritization and how to sequence our clinical development from both a medical impact and a [. .. ] degree. Research-literate. You understand clinical study design, outcome measurement, and what it takes to produce evidence that regulators and the medical community take seriously. Whether through academic research, clinical trials, or health outcomes work, you know how to build a clinical evidence base. Analytical and data-literate. You can work with datasets, interpret model outputs, and evaluate whether results make clinical sense. You dont need to write code, but youre comfortable around data and understand enough about AI and machine [. .. ]
Job am 10.04.2026 bei Jooble gefunden
Clariness GmbH
Senior Business Development Manager (m/f/d)
• Berlin Berlin, DE
We are looking for a Senior Business Development
Director based in Germany, UK, Serbia or US to join our global team and lead strategic growth across key markets. This [...]
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[...] is your opportunity to be part of a fast-scaling, tech-driven company thats redefining patient engagement, and to drive meaningful change in clinical development. Tasks Owning and driving strategic growth in your Top-Accounts and region, identifying and securing new business opportunities with pharmaceutical, biotech, and CRO partners. Building trusted client relationships with senior decision-makers in Clinical Operations, Medical Affairs, and R D. Leading the full commercial cycle-from prospecting to pitching, [. .. ] challenging projects. A supportive and open company culture, providing the opportunity to collaborate with a diverse and professional team. Impact healthcare by accelerating medical innovation through improved access to clinical trials, potentially bringing needed treatments to patients faster. At Clariness, we are proud to be an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, regardless of race, religion, gender, sexual orientation, national origin, disability or age. 88060242 [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Biontech
Director Statistical Programming (CoE-Technology Solutions)
• Berlin Berlin, DE
Führungs-/ Leitungspositionen
Are you ready to shape the future of statistical programming at Bio NTech? In this pivotal role as
Director, Statistical Programming, you will work closely with the Head of [...]
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[...] Statistical Programming to implement a cutting-edge global statistical programming ecosystem. Your expertise will drive innovation in technologies, automation, and processes, ensuring alignment with Bio NTech s mission to revolutionize healthcare while meeting regulatory standards. Join us in creating scalable, efficient solutions that empower clinical trials and data analysis in a dynamic and collaborative environment. Your Contribution: Collaborate with leadership to establish a global statistical programming ecosystem, driving vendor oversight, innovation, and alignment with company goals and regulatory requirements Lead the development and implementation of programming standards, best practices, and innovative solutions to enhance efficiency and [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Alexion Pharmaceuticals
Associate Director Country Operations Management
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
Führungs-/ Leitungspositionen
This is what you will do: The Associate
Director Country Operations Management (AD COM) reports to the Head of Country Operations. AD COM has the accountability to support the [...]
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[...] Country strategy implementation, to act as company culture and value ambassador and to act as line manager of local functions as agreed with Head of Country Operations. The AD COM [. .. ] activities at country level comply with local policies and code of ethics, and ensures team delivery to committed activation and recruitment targets Contribute to Country feasibility analysis for new potential clinical trials (as applicable, depending on the direct reports the LM will be managing) . Support the Country external scientific engagement strategy and action plan. Contribute to efficient COM organization and its functioning at country level by working closely with responsible HCO. Support HCO and in-Country COM activities as agreed 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 125 offene Stellenanzeigen für Clinical Trials Director Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Director Jobs?
Aktuell suchen 20 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 (15 Jobs)
- IQVIA (6 Jobs)
- Clariness GmbH (3 Jobs)
- Alexion Pharmaceuticals (3 Jobs)
- dehaze GmbH (2 Jobs)
- Neo Carbon (1 Job)
In welchen Bundesländern werden die meisten Clinical Trials Director Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Director Jobs werden derzeit in Bayern (20 Jobs), Hessen (16 Jobs) und Sachsen-Anhalt (15 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Director Jobs?
Clinical Trials Director Jobs gehören zum Berufsfeld Biotechnologie.
