130 Jobs für Clinical Trials Investigator
Stellenangebote Clinical Trials Investigator Jobs
Job am 22.10.2025 bei Neuvoo gefunden
Rhythm Pharmaceuticals
• Munich, Bavaria
[. .. ] internal colleagues. He/ she will support the local Hospital Affairs Lead (HAL) and will be responsible for building peer to peer relationships with external experts and other [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] stakeholders to provide clinical, scientific, and medical education in the territory. The SAM will support research initiatives, advisory boards, and other compliant scientific exchange activities to support Rhythm s strategically aligned Medical Affairs Plan aimed at identifying and addressing the unmet needs of people living with rare genetic disorders of obesity. Responsibilities and Duties [. .. ] networks to aid experts in uncovering people with rare genetic disease of obesity. Closely collaborate with Global Clinical Development and Operations on interactions with investigators participating in Rhythm s clinical trials, investigator meetings and advisory boards. Support clinical trial execution attending to the needs of investigators. Triage pressure points that may impede progress of clinical studies to the cross functional team for timely resolution. Assist in identification and education of referral sites for clinical trials and investigators to drive trial enrolment. Develop [. .. ]
Job am 20.10.2025 bei Neuvoo gefunden
Chronos Consulting
Clinical Affairs Program Manager Germany
• deutschland,
Job Description Our client is a global medical device company, a pioneer of the MR-guided focused ultrasound technology which is a game-changing innovation. They are looking for a
Clinical Affairs [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Program Manager Europe. The role is remote with up to 40 travel and based in Europe. As part of the global clinical affairs team, you will be responsible for developing strategies for a successful execution of roadmap clinical trials that demonstrate medical product safety and efficacy. Additional responsibilities include management of clinical trials approvals with local IRBs and/or Competent Authorities. Required Skills and Experience: 1) BS, BA, BSN or RN or higher degree in the Life Sciences or related disciplines 2) Minimum 3+ years in clinical management position [. .. ] abilities to operate independently 11) Willing able to travel domestically and internationally, as required (up to 40) Responsibilities: Collaborate with Company Stakeholders to execute company objectives into successful clinical trials, investigator-sponsored studies, etc. Overall responsibility for design of clinical trials including protocol development, clinical trial discussions with EU Competent Authorities, and development of timeline and budget Manage the process of screening/ qualifying, selecting, and contracting with investigators, sites and vendors required for conduct of clinical trials Direct/ Manage necessary clinical [. .. ]
Job am 20.10.2025 bei Neuvoo gefunden
Chronos Consulting
• deutschland,
Führungs-/ Leitungspositionen
Job Description Our client is a leading, global medical device company pioneering noninvasive surgical treatments. The Regional Director of
Clinical Affairs will work closely with senior management to translate business [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] commercial objectives into requirements for specific clinical trials and programs. This role is responsible for the successful execution of the EU clinical portfolio as well as the management, growth and development of the clinical staff. Skills and Experience: 1) BS, BA, BSN or RN or higher degree in the Life Sciences or related disciplines 2) Minimum 5+ years [. .. ] will be an advantage. 10) Willing able to travel domestically and internationally, as required (up to 40) Responsibilities: Strategic translation of business objectives into successful clinical requirements for clinical trials, investigator-sponsored studies, publications, etc, and by meeting EU regulatory requirements for clinical evaluations and post-market surveillance Manage and develop global internal team of Clinical Project Managers and outside vendors, as needed Overall responsibility for design of clinical trials including protocol development, clinical trial discussions with EU Competent Authorities, and [. .. ]
Job gestern bei Jooble gefunden
Study Physician sponsor dedicated in Germany
• München
Study Physician sponsor dedicated in Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] g. Internal medicine, oncology, neurology, immune-oncology, cardiology, pediatrics, emergency medicine are preferred) with following experience: Global Medical Monitor/ Study Physician/ Clinical Trial Physician managing phase I to IV clinical trials in CRO/ Pharma company. Global Project Manager/ Clinical Trial leader/ Project manager managing multiple countries in CRO/ Pharma company. Country Trial Manager/ Local Project Manager/ Project Manager USA in CRO/ Pharma company Global Safety Physician/ Risk Management Physician in Pharmacovigilance department in CRO/ Pharma company Additional Points: Clinical practice experience [. .. ] requirements too) Medical Monitoring experience preferred Pharma company experience preferred. However, CRO experience is fine. If no industry experience, the in addition to clinical practice they should have worked principal investigator/ sub investigator in clinical trials for a reasonable amount of time. Travel-15-20 depending on the study requirements. Key words to look for in potential CVs-Clinical Trial protocol-writing/ reviewing, Identify medically relevant critical data, Medical risks, risk mitigation/ monitoring plan, Medical quality review/clinical quality monitoring, Jreview, [. .. ]
Job vor 3 Tagen bei Jooble gefunden
• Berlin
The Regional Medical Science Liaison (MSL) serves as the primary field-based point of contact with healthcare providers (HCPs) including
clinical investigators on a range of clinical and scientific issues. The [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] primary role is to deliver and facilitate medical education and communications, research, and scientific insight gathering activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by [. .. ] aligned to strategy within the business Serves as external, credible scientific expert on disease area and client products at HCP field meetings, key medical and scientific conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Works to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintains and develops synergistic relationships with KOLs to expand research, advisory, and educational partnership opportunities Training of the Key Account Management Team [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Sr CRA in oncology-Sponsor dedicated-Home Based Germany
• München
Sr CRA in oncology-Sponsor dedicated-Home Based Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] each subject/ patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) :Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete via [. .. ] or applicants to perform the essential functions of the job. Summary Roles within Clinical Monitoring/ CRA job family are responsible for monitoring during clinical research studies to ensure that the trials are being conducted in accordance with widely accepted clinical practices. This includes conducting on-site and remote monitoring, developing tools, procedures, and processes to ensure quality monitoring. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities [. .. ] project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Senior Clinical Trial Assistant
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities [. .. ] project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, [. .. ]
Job vor 7 Tagen bei Jooble gefunden
University of Tübingen- Faculty of Medicine
• Tübingen
[. .. ] and University Hospital are part of the University of Excellence Tübingen. They provide medical services at the highest level and cover the entire spectrum of modern medicine, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] research, teaching and clinical care. The Faculty of Medicine at the University of Tübingen invites applications for a position at the University Clinic for Medicine, Internal Medicine VIII: Medical Oncology and Pneumology as a Professor (W3) in Translational Medical Oncology with a Focus on Thoracic Oncology (m/f/d) available immediately. The position will [. .. ] The i FIT cluster of excellence is translationally orientated and it is expected that the successful candidate will bring therapeutical concepts developed preclinically at i FIT into the clinic by means of investigator-initiated trials (IITs) . Close collaborations with the National Center for Tumor Diseases (NCT-South West) and the Tübingen Center for Academic Drug Discovery and Development (Tü CAD2) will facilitate this. In the area of teaching, extensive and excellently evaluated teaching experience and commitment are expected, especially with regard to innovative curricula of [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Study Specialist (Contract)
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities [. .. ] project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities [. .. ] project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Senior Research Associate
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities [. .. ] project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Job Description Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities [. .. ] as required. Supports remote monitoring, if and as applicable. Assists in study budget preparation and clinical study agreement execution, including ensuring necessary payments are made according to executed agreements. Negotiates investigator/ hospital agreements with stakeholders. Maintains and completes own expense reports as per local and applicable guidelines. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Qualifications Appropriate life-science or healthcare-related qualification or experience or [. .. ]
Job vor 14 Tagen bei Jooble gefunden
Thermo Fisher Scientific
Clinical Trial Coordinator II (m/f/d) - Germany
• Karlsruhe
[. .. ] safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the [. .. ] We invite you to re-imagine health promoting protocols with us, working alongside our dedicated, forward-thinking and upbeat teams. A day in the Life: Performs PPD clinical research services investigator file reviews and logging of outstanding issues in project related tracking tools Reviews regulatory documents for proper content Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD clinical research services departments [. .. ]
Job am 14.01.2026 bei Jooble gefunden
• Berlin
Absolventen, Einsteiger, Trainees
[. .. ] gifted cultivator of new and exciting opportunities grounded in science? The (Junior-) Field Medical Advisor serves as the primary field-based point of contact with healthcare providers (HCPs) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] including clinical investigators on a range of clinical and scientific issues. The primary role is to deliver and facilitate medical education and communications, research, and scientific insight gathering activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by [. .. ] aligned to strategy within the business Serves as external, credible scientific expert on disease area and client products at HCP field meetings, key medical and scientific conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings Identify key field insights related to client products, activities and the disease area and effectively disseminate and collaborate with cross-functional partners Facilitate clear communication between the business and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Essential Requirements Advanced Degree MD, Ph D, Pharm D Demonstrable experience in an MSL function with oncology desired) Knowledge of clinical research design and GCP in the oncology/ immune oncology area Demonstrate a strong understanding of clinical research trial design and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Freelance CRA Germany
• München
Freiberuflich
Freelance CRA Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. [. .. ] remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Incyte Corporation
• München
[. .. ] Medical Affairs Inflammation Autoimmunity (IAI) Team and supports the development of the local medical strategy and medical plans within the therapeutic area of dermatology. The role provides [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a bridge between Clinical Development, Medical Affairs and the commercial organization. The (Senior) Medical Manager Dermatology will play a key role in developing and executing the medical and scientific (non-promotional) strategy for the German Immunology portfolio/ therapeutic area and will be involved in a wide range of activities for Incyte IAI drugs both [. .. ] as registry/ database projects, epidemiological surveys, and PMOS studies) . Provide the required oversight to manage review, approval and conduct of IIR studies Collaborate with clinical trial teams and support investigator engagements (e. g. review new clinical study protocols, identifying potential investigators/ sites, conducting feasibility surveys) Supports adaptation of international/ local training and scientific material in collaboration with marketing and other internal stakeholders Supports development of publication plans and covers country data generation needs Provides scientific in-house training for MSLs, [. .. ] the development program, notably those relevant for the German treatment and reimbursement landscape and to address them within the country medical affairs program Knowledge in development and implementation of clinical trials and RWE programs preferred Ability to work independently and effectively in complex, rapidly changing environments Sense of urgency Flexibility, diplomacy, and the ability to manage expectations Interested in new ways of thinking and innovative approaches Ability to travel up to 25 of working time Language: German, English fluent Proficient in [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Alexion Pharmaceuticals
Clinical Research Associate
• München
This is what you will do: The
Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at their assigned sites and is an active participant [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in the local study team (s) . The CRA works in close collaboration with local team members (Project Management Clinical Operations (PMCO) , Study Start-Up (SSU) manager, Clinical [. .. ] Items aging, SDV metrics, Data entry metrics, query aging, MV reports metrics, etc. ) Preparing and finalizing monitoring visit reports in CTMS and provide timely feed-back to the Principal Investigator, including follow-up letter, within required timelines and in line with Alexion SOPs. Ensuring timely collection/ uploading of essential documents into the e TMF in accordance with ICH-GCP, Alexion SOPs and local requirements. Supporting/ participating in regular QC checks of the e TMF In some countries, as required, CRAs are accountable [. .. ] Sees change as an opportunity to improve performance and add value to the business. Ability to look for and champion more efficient and effective methods/ processes of delivering quality clinical trials with reduced budget and in less time. Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines. Proactivity and assertively when communicating with internal stakeholders and sites Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/ [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Biontech
• Berlin
Jobticket
[. .. ] aligned with local and European medical affairs priorities. Build and expand relationships/ networks with key medical and scientific experts in the field of breast cancer and/or lung [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] cancer. Support clinical trials by identifying study sites, participating in SIVs (Site Inviations Visits) , assisting with patient enrollment, and ensuring smooth information exchange. Identify research opportunities, including Investigator-Initiated Trials, Real-World Evidence, and other evidence-generation studies. Represent the organization at scientific conferences, advisory boards, and educational events, sharing insights and preparing reports for internal stakeholders. Ensure timely documentation of HCP interactions, compliance with local policies, and accurate reporting of insights and safety information. What you have [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
Local Clinical Trial Manager-FSP, Germany-6 month FTC (m/f/d)
• Homeoffice
[. .. ] safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the [. .. ] required, advises support/ develops and negotiates on contract development with Sites/ CRO/ Vendors ensuring legal input where required and may participate in budget/ contract negotiations with study vendors or clinical investigator sites. As required, selects manages local vendors in accordance with local practices in alignment with overall resourcing strategy for the study; accountable for local vendor management including oversight, agreements, payments, communications issue management. Manages the development of key study documents, plans manuals according to local requirements (monitoring plan, local informed [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
Manager, Site Engagement Liaison
• Homeoffice
Work-Life-Balance
As a Manager, Site Engagement Liaison, you will be joining the worlds largest most comprehensive
clinical research organisation, powered by healthcare intelligence. The Site Engagement Liaison Manager is a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] field based expert who supports the conduct and the patient recruitment of the client global clinical trials at investigative sites, through local and relational support. What you will be doing: Participate in study-level feasibility activities through providing key country/ regional and site specific knowledge including patient pathways and operational execution. Interface and act as a local client Trial Ops representative, an expert on the clinical trial [. .. ] signature as needed. Proactively work to fully understand all matters that impact the successful patient recruitment and high quality conduct of the clinical trial at each site, eg the Principle Investigator (PI) and site preferences and best practices on clinical trials, standard of care treatments, competing studies etc. Ensure a supportive relationship with clinical sites and trial personnel. Proactively work to fully understand the patient voice, preferences and pathway (s) . Closely work with the client GPA team. Speak to patient [. .. ]
Job gestern bei Jooble gefunden
Study Physician sponsor dedicated in Germany
• München
Study Physician sponsor dedicated in Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] g. Internal medicine, oncology, neurology, immune-oncology, cardiology, pediatrics, emergency medicine are preferred) with following experience: Global Medical Monitor/ Study Physician/ Clinical Trial Physician managing phase I to IV clinical trials in CRO/ Pharma company. Global Project Manager/ Clinical Trial leader/ Project manager managing multiple countries in CRO/ Pharma company. Country Trial Manager/ Local Project Manager/ Project Manager USA in CRO/ Pharma company Global Safety Physician/ Risk Management Physician in Pharmacovigilance department in CRO/ Pharma company Additional Points: Clinical practice experience [. .. ] requirements too) Medical Monitoring experience preferred Pharma company experience preferred. However, CRO experience is fine. If no industry experience, the in addition to clinical practice they should have worked principal investigator/ sub investigator in clinical trials for a reasonable amount of time. Travel-15-20 depending on the study requirements. Key words to look for in potential CVs-Clinical Trial protocol-writing/ reviewing, Identify medically relevant critical data, Medical risks, risk mitigation/ monitoring plan, Medical quality review/clinical quality monitoring, Jreview, [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Incyte Corporation
Medical Science Liaison Dermatology (m/f/d) - Frankfurt, Kassel, Saarbrücken
• Homeoffice
[. .. ] Liaisons, who are eager to help shape this next phase scientifically and operationally. Job Summary Medical Science Liaisons (MSLs) are a team of field-based, highly trained professionals [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with strong clinical and/or scientific backgrounds and excellent communication skills. They represent the Medical Affairs organization to the broad scientific community. Essential Functions of The Job (Key Responsibilities) Represent the company and lead medical scientific exchanges within the respective community Develop and lead Key External Experts and investigators engagement plans identify, develop [. .. ] (i. e. dermatologists) . Systematically generate, prioritize and communicate medical insights to inform medical strategy and cross-functional decision-making Lead and support advisory board meetings, round table meetings and investigator meetings. Facilitate company sponsored and investigator sponsored trials (ISTs) Actively support real-world evidence generation activities, including non-interventional studies (NIS) , registries and collaborative research projects. Closely cooperate and align with KAM-team for all activities related to medical information for external groups. Act as point of contact for unsolicited information requests on company inline products and [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Incyte Corporation
Medical Science Liaison Dermatology (m/f/d) - Münster, Dortmund, Bielefeld
• Homeoffice
[. .. ] Liaisons, who are eager to help shape this next phase scientifically and operationally. Job Summary Medical Science Liaisons (MSLs) are a team of field-based, highly trained professionals [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with strong clinical and/or scientific backgrounds and excellent communication skills. They represent the Medical Affairs organization to the broad scientific community. Essential Functions of The Job (Key Responsibilities) Represent the company and lead medical scientific exchanges within the respective community Develop and lead Key External Experts and investigators engagement plans identify, develop [. .. ] (i. e. dermatologists) . Systematically generate, prioritize and communicate medical insights to inform medical strategy and cross-functional decision-making Lead and support advisory board meetings, round table meetings and investigator meetings. Facilitate company sponsored and investigator sponsored trials (ISTs) Actively support real-world evidence generation activities, including non-interventional studies (NIS) , registries and collaborative research projects. Closely cooperate and align with KAM-team for all activities related to medical information for external groups. Act as point of contact for unsolicited information requests on company inline products and [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Medical Science Liaison Rare Disease-Ostdeutschland
• Schwerin
The Regional Medical Science Liaison (MSL) serves as the primary field-based point of contact with healthcare providers (HCPs) including
clinical investigators on a range of clinical and scientific issues. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The primary role is to deliver and facilitate medical education and communications, research, and scientific insight gathering activities of the client. This includes the provision of scientific and medical data on both licensed and unlicensed products and indications as permissible by [. .. ] aligned to strategy within the business Serves as external, credible scientific expert on disease area and client products at HCP field meetings, key medical and scientific conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Works to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintains and develops synergistic relationships with KOLs to expand research, advisory, and educational partnership opportunities Training of the Key Account Management Team [. .. ]
1 von 6Weiter » Weitere Suchergebnisse laden »
Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Investigator pro Jahr?
Als Clinical Trials Investigator verdient man zwischen EUR 60.000,- bis EUR 100.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Investigator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 130 offene Stellenanzeigen für Clinical Trials Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Investigator Jobs?
Aktuell suchen 19 Unternehmen nach Bewerbern für Clinical Trials Investigator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trials Investigator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trials Investigator Stellenangebote:
- Thermo Fisher Scientific (8 Jobs)
- Abb Vie (6 Jobs)
- IQVIA (6 Jobs)
- Incyte Corporation (3 Jobs)
- Alexion Pharmaceuticals (3 Jobs)
- Dr. Falk Pharma GmbH (2 Jobs)
In welchen Bundesländern werden die meisten Clinical Trials Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Investigator Jobs werden derzeit in Bayern (18 Jobs), Hessen (10 Jobs) und Sachsen-Anhalt (8 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Investigator Jobs?
Clinical Trials Investigator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
