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124 Jobs für Clinical Trials Director


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Job gestern bei Jooble gefunden Actalent

Medical Sciences Director

• Münster Führungs-/ Leitungspositionen [. .. ] is seeking experienced Medical Science Liaisons (MSLs) to support its Dermatology franchise. This fieldbased role sits within Medical Affairs and plays a critical part in scientific exchange, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] external expert engagement, clinical research support, and insight generation. The successful candidate will help shape the medical strategy during an important growth phase. Key Responsibilities Lead highquality medical and scientific exchange with dermatologists and other relevant stakeholders Identify, develop, and maintain longterm relationships with Key External Experts (KEEs) and investigators Support medical launch readiness [. .. ] data with external audiences Systematically collect and communicate medical insights to inform strategy and crossfunctional decisionmaking Plan and support advisory boards, investigator meetings, and roundtable discussions Facilitate companysponsored and investigatorsponsored trials (ISTs) Contribute to realworld evidence (RWE) initiatives, including noninterventional studies and registries Collaborate closely with Key Account Managers and internal medical colleagues Act as a point of contact for unsolicited medical information requests Deliver internal medical training on disease areas and emerging data Ensure strict adherence to SOPs, compliance, and [. .. ]

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Job gestern bei Jooble gefunden Hlx Life Sciences Senior Project Director • Berlin Führungs-/ Leitungspositionen Were working with a CRO whose seeking a Project Manager with 5+ years of CRO project management experience and a strong understanding of the full clinical trial lifecycle. Lead clinical [...]
MEHR INFOS ZUM STELLENANGEBOT[...] trials from study start-up through closeout-Manage sponsor relationships and cross-functional project teams-Coordinate activities across Clinical Operations and must have strong experience in Medical Writing, Data Management, and Quality Assurance-Ensure compliance with ICH-GCP, regulatory requirements, and company SOPs-Drive project success through effective communication, planning, and [. .. ]

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Job vor 5 Tagen bei Mindmatch.ai gefunden Merck Healthcare

Medical Advisor Rare Disease Austria (all genders)

• AT- 9 Wien [. .. ] for patients with rare tumors. You will define and execute the local medical strategy, drive evidence generation initiatives, build lasting relationships with key opinion leaders and patient [...]
MEHR INFOS ZUM STELLENANGEBOT[...] organizations, and support clinical development activitiesall while ensuring the highest standards of scientific integrity and regulatory compliance. Key Responsibilities Medical Strategy Scientific Expertise Define and lead the local medical strategy for your therapeutic area, aligned with global and regional objectives. Serve as the internal expert on disease biology, treatment landscape, and evolving standards of [. .. ] gathering patient insights and supporting patientcentric approaches. Plan and lead local patient organization engagement activities, including disease awareness initiatives and events at major congresses. Collaborate with the European Patient Advocacy Director to align countrylevel PAO strategy and tactics. Analyze the local patient advocacy landscape and represent the company externally at relevant meetings. Clinical Development Evidence Generation Support companysponsored clinical trials across all phases, from site identification and initiation through to completion, including patient enrollment support and investigator engagement. Act as primary liaison to investigators interested in developing and conducting investigatorinitiated research (IIS) ; coordinate between investigators and internal stakeholders. Drive realworld evidence (RWE) generation and lead/support local medical studies; [. .. ]

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Job am 29.05.2026 bei Mindmatch.ai gefunden IQVIA Argentina Remote Local Study Director-Clinical Trials Lead • AT- 9 Wien Führungs-/ Leitungspositionen Vienna, Austria Full time Home-based R1546726 To lead Local Study Teams (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying [...]
MEHR INFOS ZUM STELLENANGEBOT[...] with Sponsor Procedural Documents, international guidelines such as ICHGCP as well as relevant local regulations. In addition to leading LST (s) , the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model. The Local Study Associate Director is responsible to ensure that sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived. MAIN RESPONSIBILITIES Has the overall responsibility for the study commitments within the country and [. .. ] Affairsled or Academicled studies) . Good knowledge of international guidelines ICH GCP as well as relevant local regulations. Proven ability to lead and motivate cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality. Good medical knowledge of Oncology, Rare Diseases, cardiology, hematology, CVRM Therapeutic Areas. Good knowledge of the Drug Development Process. Excellent understanding of the Clinical Study Process including monitoring. Very good understanding of the Study Drug Handling Process and [. .. ]

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Job am 29.05.2026 bei Mindmatch.ai gefunden IQVIA Argentina

Local Study Associate Director

• AT- 9 Wien Führungs-/ Leitungspositionen Vienna, Austria Full time Home-based R1546726 To lead Local Study Teams (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying [...]
MEHR INFOS ZUM STELLENANGEBOT[...] with Sponsor Procedural Documents, international guidelines such as ICHGCP as well as relevant local regulations. In addition to leading LST (s) , the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model. The Local Study Associate Director is responsible to ensure that sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived. MAIN RESPONSIBILITIES Has the overall responsibility for the study commitments within the country and [. .. ] Affairsled or Academicled studies) . Good knowledge of international guidelines ICH GCP as well as relevant local regulations. Proven ability to lead and motivate cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality. Good medical knowledge of Oncology, Rare Diseases, cardiology, hematology, CVRM Therapeutic Areas. Good knowledge of the Drug Development Process. Excellent understanding of the Clinical Study Process including monitoring. Very good understanding of the Study Drug Handling Process and [. .. ]

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Job am 27.05.2026 bei Mindmatch.ai gefunden St. Anna Kinderkrebsforschung Principal Investigator (f/m/d) - Translational Medicine for Pediatric Cancer • W wien [. .. ] therapeutic options for children with cancer At St. Anna Childrens Cancer Research Institute (St. Anna CCRI) , translational medicine is driven by a single purpose: turning scientific [...]
MEHR INFOS ZUM STELLENANGEBOT[...] insight into tangible clinical impact for pediatric cancer patients. To further strengthen our portfolio in translational discovery and therapeutic development, we are seeking an outstanding Principal Investigator in Translational Medicine for Pediatric Cancer. This position is open to candidates at different career stages from emerging group leaders to experienced Principal Investigators. In this role, [. .. ] into clinical concepts: Integrate research findings with precision oncology initiatives to enable biomarkerinformed and clinically relevant therapeutic strategies. Strengthen earlyphase translational interfaces: Collaborate closely with the St. Anna CCRI Clinical Trials Unit, Statistics, and St. Anna Childrens Hospital to support robust preclinicaltoclinical translation. Build and lead a multidisciplinary research team: Recruit, mentor, and guide scientists while ensuring scientific rigor, reproducibility, and regulatory alignment. Ensure visibility, collaboration and sustainability: Secure competitive thirdparty funding, publish highimpact research, and represent St. Anna CCRI in [. .. ] on predefined core criteria relevant to the position. Virtual interviews with the Scientific Directors: Shortlisted candidates are invited to participate in two separate virtual oneonone interviews one with each Scientific Director of St. Anna CCRI. Onsite hearing (18-20 September 2026) : The highestranked candidates are invited to an onsite hearing at St. Anna CCRI. Offer final negotiations: Following the hearing, negotiations are conducted with the topranked candidate, and the final appointment decision is made based on the overall evaluation and [. .. ]

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Job am 27.05.2026 bei Mindmatch.ai gefunden St. Anna Kinderkrebsforschung

Principal Investigator (f/m/d) Cellular Immuno-Therapies

• W wien [. .. ] you will establish and lead an internationally competitive research program at the forefront of engineered immune cell therapies and cancer vaccines, driving breakthroughs from discovery through preclinical [...]
MEHR INFOS ZUM STELLENANGEBOT[...] validation to early clinical translation, within a uniquely integrated benchtobedside-and-back environment. Establish and lead an independent research program in cellular or immuno-therapies: Develop innovative approaches in one or more core areas of cellular and immuno-therapy (e. g. engineered T/ NK cells, CAR-based strategies, next-generation cell-based approaches, or [. .. ] with a clear emphasis on scientific depth and differentiation within a defined focus area. Drive translational innovation from discovery to clinic: Advance immuneengineering concepts through preclinical validation toward earlyphase clinical trials in close alignment with precision oncology initiatives. Strengthen clinical and translational interfaces: Collaborate closely with the St. Anna CCRI Clinical Trials Unit, pediatric oncology teams, and GMP facilities at partnering institutions to align research, manufacturing, and regulatory pathways. Advance next-generation immune engineering technologies: Lead scientific innovation in immune cell [. .. ] on predefined core criteria relevant to the position. Virtual interviews with the Scientific Directors: Shortlisted candidates are invited to participate in two separate virtual oneonone interviews one with each Scientific Director of St. Anna CCRI. Onsite hearing (18-20 September 2026) : The highestranked candidates are invited to an onsite hearing at St. Anna CCRI. Offer final negotiations: Following the hearing, negotiations are conducted with the topranked candidate, and the final appointment decision is made based on the overall evaluation and [. .. ]

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Job am 27.05.2026 bei Mindmatch.ai gefunden St. Anna Kinderkrebsforschung Head of Precision Oncology (f/m/d) • W wien Führungs-/ Leitungspositionen Where cuttingedge science meets real clinical decisions, precision oncology makes the difference Precision oncology has the power to redefine how children with cancer are diagnosed and treated and at [...]
MEHR INFOS ZUM STELLENANGEBOT[...] St. Anna Childrens Cancer Research Institute (St. Anna CCRI) , we are taking this promise to the next level. To strategically expand our institutional precision medicine program, [. .. ] patients. Drive innovation and technology development: Implement nextgeneration sequencing, data analytics, and functional precision medicine approaches. Strengthen translational and clinical trial interfaces: Collaborate closely with the St. Anna CCRI Clinical Trials Unit, the clinical diagnostics laboratory Labdia (St. Anna CCRI subsidiary) , and oncology teams (i. e. , national and international PIs at the St. Anna Childrens Hospital) to support biomarker-driven studies, patient selection, and early-phase translation. Leadership, visibility sustainability: Build and lead a highperforming multidisciplinary team, represent the [. .. ] on predefined core criteria relevant to the position. Virtual interviews with the Scientific Directors: Shortlisted candidates are invited to participate in two separate virtual oneonone interviews one with each Scientific Director of St. Anna CCRI. Onsite hearing (12-14 September 2026) : The highestranked candidates are invited to an onsite hearing at St. Anna CCRI. Offer final negotiations: Following the hearing, negotiations are conducted with the topranked candidate, and the final appointment decision is made based on the overall evaluation and [. .. ]

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Job vor 10 Tagen bei Jobleads gefunden

Global Medical Director, Evidence Generation Lead

• Baar, Rheinland- Pfalz Führungs-/ Leitungspositionen Global Medical Director, Evidence Generation Lead About This Role: As the Global Medical Director, Evidence Generation Lead, you will play a pivotal role in advancing data generation initiatives for [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the Dravet Syndrome therapeutic area. This position resides within the Global Medical Dravet Syndrome team and is central to driving collaboration, innovation, and excellence [. .. ] realworld evidence (RWE) studies. Lead and support Integrated Evidence Generation Planning (IEGP) forums, ensuring crossfunctional alignment and excellence in execution. Direct the design and analysis of phase 4 Company Sponsored Clinical Trials and secondary data analysis from realworld data. Lead the collaboration with the R D team and Global Value Access team on data analytics initiatives (e. g. , outcomes on subgroups, correlation of endpoints) , including registry studies, HEOR databases, and posthoc analyses. Partner with the scientific communication lead to craft [. .. ]

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Job am 08.06.2026 bei Jobleads gefunden Medical Director, Safety Clinical Trial Pharmacovigilance • Lausanne, Waadt Führungs-/ Leitungspositionen Nespresso Deutschland Gmb H in Lausanne, Switzerland is seeking a Medical Director for Clinical Trial/ Research Safety. You will take the lead in safety management for clinical development [...]
MEHR INFOS ZUM STELLENANGEBOT[...] programs and ensure compliance with pertinent regulatory frameworks. The ideal candidate will possess a medical degree (Md/Ph D) , at least 5 years of experience in clinical research and safety, and proven capabilities in managing safety in complex trials. This position requires strong strategic acumen and the ability to collaborate across teams. #J-18808-Ljbffr 94419235 [. .. ]

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Job am 08.06.2026 bei Jobleads gefunden

Medical Director Safety

• Lausanne, Waadt Führungs-/ Leitungspositionen Position Summary 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ] 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 [. .. ]

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Job am 06.06.2026 bei Jobleads gefunden Director Medical Affairs Strategic Markets EMEA Electrophysiology (m/f/d) • Hamburg Führungs-/ Leitungspositionen Purpose The Director Medical Affairs Strategic Markets EMEA Electrophysiology will oversee the Medical Scientific Liaison (MSL) team supporting the G5 markets (Germany, France, UK, Italy, and Spain) , develop [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and execute the vision, mission and goals for the Strategic Markets in EMEA, shape medical direction for Electrophysiology, ensure regulatory compliance, and serve as [. .. ] Conduct career development conversations and coaching. Provide leadership and direction to MSLs and serve as liaison for team collaborations and stakeholder engagement. External Engagements Build strong relationships with top academic clinical physician leaders in Electrophysiology and related fields. Develop and sustain relationships with KOLs, ad boards, physicians, academic institutions, FDA, EMA. Collaborate with EPs and KOLs to identify unmet needs and define solutions for strategic partnerships. Articulate value proposition of innovation externally and defend in competitive environment. Provide appropriate messaging to [. .. ] a matrix organization and ability to influence without direct authority. High emotional intelligence and interpersonal skills. Required Preferred Skills Required: Analytical Reasoning, Business Requirements Analysis, Clinical Research and Regulations, Clinical Trials Operations, Communication, Developing Others, Digital Culture, Digital Literacy, Healthcare Trends, Inclusive Leadership, Leadership, Medical Affairs, Medical Communications, Medical Compliance, Product Strategies, Stakeholder Analysis, Strategic Thinking, Workflow Analysis. Preferred: (additional skills as identified) . Compensation The anticipated pay range in the primary posting location is 119, 200.00 205, 620.00. [. .. ]

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Job am 06.06.2026 bei Jobleads gefunden

DACH Pharma Medical Patient Affairs Director

• Freiburg im Breisgau, Baden- Württemberg Führungs-/ Leitungspositionen [. .. ] the local level, ensuring alignment with the specific needs of the country. Collect the needs and insights of its territories to report them to the Corporate through [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the TOP5/ Region Director. Guarantee the deployment of the medical plan in the country to which he/ she is attached: Identify and promote innovative approaches to meet the medical challenges of the country to which he/ she is attached. Set up and manage clinical study projects and coordinate projects with health professionals (I3S and IINIS) in the country to which he/ she is attached. Generate all content and orchestrate the omnichannel dissemination of medical data. Guarantee the implementation and proper execution of clinical study projects carried out by the Corporate having part of their [. .. ] level university scientific degree, ideally in medicine with a state examination, a medical licence At least 10 years experience in the pharmaceutical industry and experience in the field of clinical trials of medicinal products Medical knowledge of the indications being treated (particularly oncology) and of the medicinal products used, including their indications and pharmacological profiles Excellent industry knowledge Extensive knowledge in the field of oncological (CRC, NSCLC, MELANOMA) and haematological therapy, as well as sufficient knowledge of therapies related to gynaecological, [. .. ]

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Job am 25.05.2026 bei Jobleads gefunden Medical Director (MD) , Multiple Sclerosis • Basel, Basel- Stadt Führungs-/ Leitungspositionen Position Roches Clinical Development organization is structured by therapeutic area and is responsible for developing and executing late-stage development (Phase IIIII) clinical strategies that deliver medically differentiated therapies for [...]
MEHR INFOS ZUM STELLENANGEBOT[...] patients. We are seeking a highly motivated Medical Director to join our Neuroimmunology team, specifically focusing on Multiple Sclerosis (MS) . This is a junior to midlevel individual contributor position without people management responsibilities. Opportunity As a Medical Director, you will participate in or lead the development of Clinical Development (CD) plans, ensuring the effective execution of strategies for [. .. ] teaching background is a plus) alongside preferred prior industry experience in MS clinical development (2 years) or recognition as an MS field expert (e. g. , Assistant Professor) . Clinical Trials Regulatory Knowledge: Significant experience designing/ conducting clinical trials, a strong understanding of Phase IIIII drug development, and required knowledge of GCP, ICH, FDA, and EMA guidelines (preferred for entrylevel candidates) . Communication Interpersonal Skills: Outstanding written and verbal communication skills to present complex data, paired with the ability to build [. .. ]

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Job am 13.05.2026 bei Jobleads gefunden

Director, Market Access-DACH

• Berlin 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. Position Summary The Director of Market Access is responsible for defining and executing the market access, pricing, and reimbursement strategy for Corcepts oncology portfolio in Germany. This role ensures timely, sustainable, and compliant patient access through navigation of Germanys complex access environment, including AMNOG, IQWi G, GBA, Statutory Health Insurance negotiations, and regional dynamics. Responsibilities [. .. ]

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Job am 11.05.2026 bei Jobleads gefunden Medical Director Multiple Sclerosis • Basel, Basel- Stadt Führungs-/ Leitungspositionen The Position Medical Director focusing on multiple sclerosis. The Opportunity In this role, you will lead and/or support earlystage clinical projects from entry into a human through proof [...]
MEHR INFOS ZUM STELLENANGEBOT[...] of mechanism and proof of concept, to transform molecules into new medicines in an area with huge unmet medical needs. Lead and/or support crossfunctional teams to design and execute clinical development plans from Phase 1 through Phase 2 (proofofconcept) Coach Clinical [. .. ] 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 5years of experience [. .. ]

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Job am 17.04.2026 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, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] execution, 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 [. .. ]

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Job am 29.03.2026 bei Jobleads gefunden Medical Director Multiple Sclerosis • 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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, [. .. ]

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Job am 21.01.2026 bei Jobleads gefunden Director of Pathology (m/f/d) • 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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Job am 15.01.2026 bei Jobleads gefunden Senior/ Medical Director (Ophthalmology) 0.5 FTE 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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) [. .. ]

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Neu Job vor 3 Std. bei Jobleads gefunden Biopharma Partnerships Director for Rare Disease Trials • Vaud Führungs-/ Leitungspositionen Unilabs, based in Vaud, Switzerland, seeks a Business Development professional to drive pipeline generation for clinical trials in Rare Diseases and Oncology. You will identify potential clients and negotiate [...]
MEHR INFOS ZUM STELLENANGEBOT[...] complex contracts between Biopharma and clinical data services. This role demands 5-10+ years of experience in sales, fluency in English, and a deep understanding of clinical trials. The position offers a hybrid working model and competitive compensation. [. .. ]

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Job gestern bei Jobleads gefunden Medical Science Liaison, Germany • Dresden, Sachsen Location (s) : Saarbrücken, Germany; Frankfurt, Germany; Würzburg, Germany; Kassel, Germany; Leipzig, Germany; Dresden, Germany Level of position: Senior Manager Position type: Field Reporting Line: Medical Director, Germany How [...]
MEHR INFOS ZUM STELLENANGEBOT[...] will your role help us transform hope into reality? The Medical Science Liaison (MSL) is a field-based scientific and clinical expert who strategically supports the medical objectives of Blueprint Medicines development programs. The MSL is responsible for identifying, developing, and managing peer-to-peer relationships with a variety of healthcare providers, including hematologists, oncologists, pathologists, dermatologists, gastroenterologists, and allergists/ immunologists, as well as basic scientists, in academic and community hospitals. [. .. ] with HCPs. Accurately profile country and define local dynamics related to patient diagnosis and referral for treatment Deliver medical/ scientific presentations to internal external stakeholders Assist with company-sponsored clinical trials and facilitation of investigator-initiated trials (ISTs) Lead planning and execution of regional advisory boards Collaborate with cross functional partners on internal projects and external initiatives Provide educational meeting support at scientific congresses Support training of cross functional teams Adhere to corporate and healthcare compliance guidance in all activities, including [. .. ]

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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 124 offene Stellenanzeigen für Clinical Trials Director Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Director Jobs?

Aktuell suchen 17 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:


  • St. Anna Kinderkrebsforschung (3 Jobs)
  • IQVIA Argentina (2 Jobs)
  • IQVIA (2 Jobs)
  • Astra Zeneca (2 Jobs)
  • Actalent (1 Job)
  • Hlx Life Sciences (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 (13 Jobs), Rheinland-Pfalz (13 Jobs) und Sachsen-Anhalt (12 Jobs) angeboten.


Zu welchem Berufsfeld gehören Clinical Trials Director Jobs?

Clinical Trials Director Jobs gehören zum Berufsfeld Biotechnologie.


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