130 Jobs für Clinical Study Manager
Stellenangebote Clinical Study Manager Jobs
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Amplity
• AT- 9 Wien
[. .. ] Site Engagement (GPSE) Reports to Program Director, Amplity Health Location Home based anywhere in Germany or Austria Territory DACH, Israel, Turkey, 60 travel Therapeutic Areas Oncology and [...]
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[...] Neurology Individual or Manager Individual We are seeking an experienced Clinical Trial Liaison (CTL) to lead site engagement strategies and patient-focused initiatives. Join a dynamic team dedicated to improving operational excellence and inclusivity in clinical trials, while building strong relationships with healthcare providers and key opinion leaders (KOLs) . Key Responsibilities Develop peer-to-peer relationships with KOLs, Principal Investigators, [. .. ] functional teams to create site engagement plans and meet clinical operations objectives. Deliver educational presentations and support healthcare professionals in surrounding communities. Share insights from clinical trial sites to inform study strategies. Scientific Expertise Maintain deep knowledge of therapeutic areas, emerging research, and disease management trends. Serve as a scientific resource, providing clinical presentations and facilitating peer-to-peer discussions. Support medical congress staffing, advisory boards, and study-specific material development. Compliance And Professional Standards Adhere to national and local codes [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Gouya Insights
Clinical Research Associate (CRA)
• AT- 9 Wien
Job Description
Clinical Research Associate (CRA) at GOUYA INSIGHTS Are you an experienced Clinical Research Associate (CRA) looking to further strengthen your expertise in clinical trial execution? Gouya Insights is [...]
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[...] seeking a motivated and handson CRA to join our growing clinical operations team. In this role, you will be responsible for onsite and [. .. ] maintaining a strong focus on sitelevel excellence, you will feel right at home at Gouya Insights. What you will be responsible for: Perform clinical monitoring activities in compliance with ICHGCP, study protocols, SOPs, and applicable regulations Serve as the primary point of contact for assigned study sites, ensuring effective communication between sites, sponsors, and involved parties Manage and track regulatory authority, ethics committee, and hospital submissions, including CTIS followup and approval tracking Support clinical project management activities, such as timelines, trackers, [. .. ] Medical, or Pharmaceutical studies, or an equivalent combination of education and experience Proven experience with regulatory authority, ethics committee, and hospital submissions Willingness and motivation to expand into clinical project manager responsibilities Excellent command of English (written and spoken) and working proficiency in German (B2 level or higher) Good teamwork skills Problemsolving skills Results and detailoriented approach to work delivery and output Ability to prioritize own workloads to meet deadlines Strong software and computer skills, including MS Office applications Ability to [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
SCARLETRED Holding GmbH
• AT- 9 Wien
SCARLETRED Holding Gmb H is a global leader in standardized skin imaging and AI-driven skin analysis, providing cutting-edge software products and services tailored to biopharma, biotech, cosmetics companies,
clinical research [...]
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[...] organizations, and healthcare professionals. Our flagship product, Scarletred Vision, is an ICH-GCP and EU-GDPR compliant mobile medical device software that standardizes and digitizes skin assessments in pre-clinical, clinical, and post-marketing studies. The platform enables easy, scalable, remote, and on-site monitoring of dermatologic conditions while [. .. ] innovative solutions that enhance efficiency and precision in skin research and analysis. Role Description This is a 100 on site role in our headquarter in Vienna for a Customer Success Manager position (Biopharma/ Clinical Research) . Responsibilities include overseeing clinical projects and ensuring timely setup of our system, supply of our services and overall project execution, managing customer relationships to ensure satisfaction and retention, and support developing strategies to improve the customer experience. The role requires collaboration with internal teams, providing [. .. ] to clients in Biopharma and acting as a liaison between customers and the company to address inquiries and feedback effectively. Key Responsibilities Plan, coordinate, and manage clinical research projects and study timelines Serve as the primary contact for sponsors, CROs, and external partners Build strong customer relationships with a focus on satisfaction, retention, and long-term trust Prepare, organize, and maintain study and project documentation Track project progress, report key developments internally, and identify improvement opportunities Collaborate cross-functionally with internal [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
PSI CRO
Central Monitoring Manager
• AT- 9 Wien
[. .. ] moving forward, the central monitoring function has become a top priority at PSI. We are looking for a person, who would lead the risk-based monitoring approach implementation [...]
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[...] on the clinical study and program level to ensure patient safety and data integrity. You will: Lead and facilitate initial and ongoing study Risk Management Participate in selection and setup of the RBM platform Perform Centralized Monitoring for a study including review of Key Risk Indicators, Statistical Analyses and Quality Tolerance Limits Present Centralized [. .. ] Communicate study challenges to Clinical Data Science group and work out data-driven solutions Qualifications College/ University degree or an equivalent combination of education, training and experience Clinical Study Lead/Manager experience Strong communication presentation skills are essential Leadership and ability to work independently are essential Centralized Monitoring experience is a plus Critical thinking and analytical skills Ability to work with complex data and provide insight into risk reports and trends Ability to adapt to changing circumstances and learn quickly Knowledge [. .. ]
Job am 11.03.2026 bei Mindmatch.ai gefunden
Teleflex
• AT- 9 Wien
Expected Travel: More than 50 Requisition ID: 13617 Position Summary The
Clinical Research Associate (CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable [...]
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[...] regulatory standards (MDR, ISO 14155, ICH/ GCP guidelines, Teleflex procedures and IRB/ EC policies) . The CRA conducts monitoring visits as identified by the monitoring plan, study team or department needs to evaluate data accuracy and subject safety required by review of regulatory documents, medical records, reported data and device storage, if applicable. The CRA must be able to identify issues, present findings to the site staff, provide retraining if needed, provide problemsolving strategies and communicate findings [. .. ] in respect to safetyrelated documents used and to safety event reporting processes. Collects local data protection requirement information and reports to CPM prior to study start. Assists the Clinical Project Manager department and studyrelated projects as requested including inhouse audits, investigator meetings, training, etc. Conducts comonitoring with Clinical Studies personnel to confirm monitoring is conducted consistently with the protocol, department SOP, WIs and monitoring plans and regulatory standards. Oversees training of newly hired Clinical Studies personnel and provides leadership performing daytoday [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Alimentiv
Join our Talent Pool-Clinical Research Associates (Eastern Europe)
• AT- 9 Wien
[. .. ] quite matches what youre looking for, or not ready to make a move yet? Let us know We are proactively inviting qualified candidates to join our talent [...]
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[...] pool for anticipated Clinical Research Associate needs (across multiple seniority levels) to support our Clinical Monitoring team. What the process looks like: A Talent Acquisition representative will contact selected candidates to schedule a qualifying call to learn more about your experience, and what your timeline looks like Well also share details about timelines on [. .. ] system reviews (EDC, CTMS, RBM, TMF) to ensure data quality, completeness, and regulatory compliance. Assist/ lead (as appropriate) with query resolution, safety reviews, and adverse event follow-up throughout the study lifecycle. Support/ conduct (as appropriate) site startup and activation activities, including investigator coordination, trial material delivery, and recruitment support. Maintain accurate, timely, and complete TMF documentation, requesting updates as required. Provide day-to-day operational support to Senior CRA, and Lead CRAs. Participate in training, study meetings, and CRA development [. .. ] competencies required for role progression. Sr. Clinical Research Associate As above, with the addition of the following: Act as subject matter expert, mentor, coach and/or provide performance feedback to manager for peers. Assist with selection, hiring, training, and supervision of CRAs as needed. Perform co-monitoring and training visits with CRAs. When required, act as the first escalation point for the resolution of site/ patient issues or to address Sponsor concerns. May represent Director, Monitoring and Site Management or Manager, [. .. ]
Job am 16.02.2026 bei Mindmatch.ai gefunden
SCARLETRED Holding GmbH
• AT- 9 Wien
A leading medical technology firm is seeking a Customer Success
Manager to manage
clinical trial projects and foster communication with clients in the biopharma and cosmetics industries. You [...]
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[...] will be responsible for project success, planning, onboarding, and acting as the primary contact for study sponsors. The position requires a minimum of 2 years in clinical project management, excellent organizational skills, and fluent English. This is a full-time, on-site role located in Vienna, Austria, with a gross annual salary starting at EUR 45, 000. J-18808-Ljbffr 80873735 [. .. ]
Job am 15.02.2026 bei Mindmatch.ai gefunden
SCARLETRED Holding GmbH
Customer Success Manager
• AT- 9 Wien
[. .. ] edge AI-powered data analysis Services, that make it possible to standardize the process of skin imaging, objectify disease and treatment assessment, and to accelerate data collection and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] analysis in clinical trials and medical routine. We are growing and seeking new, experienced and hands-on team members who think outside of the box, deliver unique ideas and like to work in a fast-paced digital health and medical research environment. You are reliable, ambitious, your heart beats for clinical trials, digital [. .. ] and artificial intelligence. You like to prove yourself and like to work in an international team and highly collaborative job environment. Job brief: We are looking for a Customer Success Manager who has proven job experience in managing clinical trials, ideally also digital health project. In this job you will support our project management activities and foster our excellent communication with our clients and partners in biopharma, cosmetics and medical industry. You will act as a bridge to our customers and [. .. ] new customers Support with planning, onboarding of new preclinical and clinical projects Prepare and carry out and (re) training calls with existing and new users Act as primary contact for study sponsors, CROs and clinical PM Management of study timelines and collect customer feedbacks Writing, organisation and management of project related documents Internal reporting of project progress to our CP Mand C-level Continuous (self) education in relevant fields Manage tickets and priorities Requirements: Minimum 2 years experience in clinical project [. .. ]
Job am 08.04.2026 bei Jobleads gefunden
• Berlin
Jobticket
Munich, Germany full time Job ID: 10560 About the Role: As a
Manager Medical Science Liaison Oncology, your main role is to establish collaborations with external healthcare professionals/ experts, [...]
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[...] scientific opinion leaders and institutions to share and discuss evidencebased medical and scientific information about our oncology portfolio. You act as the field subject matter expert in oncology, while planning and executing stakeholder engagement [. .. ] field medical expert, delivering continuous medical education to HCPs (Healthcare professionals) in Germany and gathering actionable insights to inform strategy. Build and maintain scientific partnerships with key opinion leaders, Cooperative Study Groups, medical associations, and research organizations in oncology. Develop and execute an MSL Oncology strategy 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 cancer. Support clinical trials by identifying study sites, participating in SIVs (Site Initiation Visits) , assisting with patient enrollment, and ensuring smooth information exchange. Identify research opportunities, including Investigator Initiated Trials, Real World Evidence, and other evidencegeneration studies. Represent the organization at scientific conferences, advisory boards, and educational events, sharing insights and preparing [. .. ]
Job am 23.11.2025 bei Jobleads gefunden
Medical Science Liaison Manager, Nephrology, North-West
• München, Bayern
Medical Science Liaison
Manager, Nephrology, North-West Alexion Pharmaceuticals, Inc. Responsibilities Develop and maintain peer-to-peer collaborations with key medical experts in nephrology and adjacent specialties within the assigned region and [...]
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[...] become recognized and educate the medical community with up-to-date medical and scientific information. Identify and execute collaboration opportunities between expert KOLs in nephrology and Alexion medical affairs and clinical development such as publications, investigator-initiated trials, regional advisory boards, training and speaker development programs. Communicate experts opinion, feedback on new data and clinical trends to Alexion Medical Affairs, therapeutic area (TA) franchises and translate this information into strategic recommendations to enhance science and advance patient care. Respond to unsolicited [. .. ] in the region, manage questions, liaise with headquarters to ensure proper response has been provided and ensure that data is fair and balanced. In conjunction with clinical operations perform clinical study feasibility and support effective study implementation. Deliver quality medical education presentations in a variety of settings and obtain valuable feedback that can be disseminated throughout the organization e. g. Staff Meetings, Round Tables, Hospital Meeting activities. Serve as an Alexion-internal expert in therapeutic area demonstrating up-to-date and [. .. ]
Job am 23.11.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] within a geographic area. He/ she manages and maintains collegial and professional relationships with KOLs and identifies and facilitates collaboration opportunities with Alexion. He/ she combines strong [...]
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[...] business acumen and clinical expertise and serves as a peer-to-peer liaison internally and externally. He/ she ensures a close working relationship with all functions in their region, including sales, and market access. Responsibilities Develop and maintain peer-to-peer collaborations with key medical experts in nephrology and adjacent specialties within the assigned [. .. ] in the region, manage questions, liaise with headquarters to ensure proper response has been provided and ensure that data is fair and balanced. In conjunction with clinical operations perform clinical study feasibility and support effective study implementation. Deliver quality medical education presentations in a variety of settings and obtain valuable feedback that can be disseminated throughout the organization e. g. Staff Meetings, Round Tables, Hospital Meeting activities. Serve as an Alexion-internal expert in therapeutic area demonstrating up-to-date and [. .. ]
Job gestern bei Jooble gefunden
Working Student (f/m/d) Content Creation for Clinical Marketing
• Landkreis Forchheim; Region Oberfranken- West, Bayern; Regierungsbezirk Oberfranken; Bayern
Werkstudenten
[. .. ] zone in order to grow personally and professionally. Sound interesting? Then come and join our global team as Working Student (f/m/d) in the field of Content Creation [...]
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[...] for Clinical Marketing at Image Guided Surgery and Robotics. Choose the best place for your work Within the scope of this position, it is possible, in consultation with your manager, to work mobile (within Germany) up to an average volume of 60 of the respective working hours. Your tasks and responsibilities: You support the creation of professional Power Point presentations for congresses, sales teams, leadership and planning, edit and produce videos (educational content, product stories, training videos) You read clinical study summaries prepared by the team and help translate them into accessible communication materials You develop and maintain together with us internal training content that enables our commercial teams to confidently discuss clinical evidence You help write customer success stories for social media and websites You contribute fresh ideas for how [. .. ]
Job gestern bei Jooble gefunden
• Landkreis Forchheim; Region Oberfranken- West, Bayern; Regierungsbezirk Oberfranken; Bayern
Werkstudenten
[. .. ] comfort zone in order to grow personally and professionally. Sound interesting? Then come and join our global team as W orking Student (w/m/d) to help us in [...]
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[...] the Clinical Marketing department (Image Guided Surgery and Robotics) . Choose the best place for your work Within the scope of this position, it is possible, in consultation with your manager, to work mobile (within Germany) up to an average volume of 60 of the respective working hours. Your tasks and responsibilities: You will support us with reading, analysing and summarising clinical trials and scientific publications relevant to our product portfolio in the fields of orthopaedics, traumatology, spinal surgery and vascular surgery You will help translate clinical findings into accessible language, explain study design, endpoints and key findings to non-specialist colleagues, and assist in the creation of training materials with a strong clinical focus You will contribute to the creation of professional Power Point presentations for internal and external audiences You will assist in the design and creation of internal training materials [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Calyx
Senior Project Manager, Medical Imaging
• Berlin
We re on a mission to change the future of
clinical research. At Perceptive, we help the biopharmaceutical industry bring medical treatments to the market, faster. Our mission is [...]
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[...] to change the world but to do this, we need people like you. Key Responsibilities Project Management Owns resolution and decision-making for medium to complex studies, applying senior judgement to navigate [. .. ] Leads in the assessment, development, documentation and implementation of changes based on requests for change. Contribute to the improvement of policies and procedures by identifying gaps, risks, or inefficiencies at study level and partnering with cross functional stakeholders to drive practical change. Business Risk Identifies, assesses and manages risks to the success of the project. Project Monitoring and Reporting Regularly reviews the study status reports which may include status of site qualification, image processing, result reporting, and query management across all [. .. ]
Job vor 2 Tagen bei Jooble gefunden
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern
[. .. ] organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem [. .. ] site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines. Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/ patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related [. .. ] off visits for junior CRA staff, as assigned. May be mentored and assigned clinical operations lead tasks under supervision of an experienced Clinical Operations Lead (COL) , or operational line manager. Qualifications: Bachelors degree or RN in a related field or equivalent combination of education, training and experience Experience as a CRA in oncology trials. Knowledge of Good Clinical Practice/ ICH Guidelines and other applicable regulatory requirements Must demonstrate good computer skills and be able to embrace new technologies Excellent communication, [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Indero
Project Manager II (Germany)
• Unstrut- Hainich- Kreis; Thüringen Thueringen
Description The project
manager II has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned
clinical trials. The project manager II oversees [...]
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[...] and coordinates study resources to ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard operating procedures (SOPs) , good clinical practices, regulatory and study-specific requirements. Project Manager II acts as the main line of communication to relevant stakeholders and provides input to feasibility, study design, [. .. ]
Job vor 9 Tagen bei Jooble gefunden
Linical
• Deutschland Deutschland, DE
The
Clinical Research Associate is responsible for the feasibility, initiation, monitoring, and close-out of investigative sites. Major responsibilities include ensuring the safety and well-being of
study participants at [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] assigned sites, ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through source data verification and monitoring process, and ensuring site compliance with all Investigational Product (IP) storage, inventory, dispensing, dosing, and disposition requirements. EU CRAs could have a shared role of Regulatory Affairs Officer (RAO) and CRA. The Regulatory department will oversee the RAO role while the Clinical Operations Manager (COM) will oversee the CRA role. Duties and Responsibilities Participates in the identification of potential investigative sites, conducts site qualification visits, collects, and reviews site regulatory documents, and prepares site qualification visit reports and associated documentation; participates in the final selection of investigative sites Conducts site initiation visits; trains site [. .. ]
Job vor 9 Tagen bei Jooble gefunden
Universitätsklinikum Freiburg
Data Manager (m/f/d)
• Region Südlicher Oberrhein, Württemberg; Regierungsbezirk Freiburg; Württemberg Freiburg im Breisgau, DE
Jobticket
The
Clinical Studies Centre of the University Hospital Freiburg is seeking to fill a position as soon as possible. Data
Manager (m/f/d) The Center for Clinical Studies is [...]
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[...] a central facility of the University Hospital Freiburg. It offers comprehensive and professional services to science and industry in the planning, execution, and evaluation of clinical trials in accordance with applicable regulations and the internationally recognized quality standards of Good Clinical [. .. ] shop and other discounts. An insight into your tasks: Design, programming, validation and maintenance of clinical databases and online questionnaires (e CRFs) Data cleaning including query management Creation and maintenance of study-specific data management documents Coordination of data management activities with participating clinicians, statisticians, monitors, project managers and our external study partners Our requirements for you: Completed studies or training in the field of medical documentation, medical information management or comparable qualifications. Programming skills in SAS and SQL Knowledge of e CRF [. .. ]
Job am 25.04.2026 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 aspects, as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 with [. .. ] the development of departmental strategies Provide guidance to Statistical Programmers on SDTm/ADa M and TLFs specifications development and programming Provide input to database requirements and work closely with Clinical Data Manager to ensure data quality standards are met What you have to offer: Ph D or Masters in (Bio) Statistics, Mathematics or equivalent Minimum 5 years (8 years for masters) in the pharmaceutical industry and/or CRO At least 3 years of work/ leadership experience, overseeing statistics staff (internal as well as [. .. ]
Job am 25.04.2026 bei Jooble gefunden
Clinical Trial Manager
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
Clinical Trial
Manager Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, [. .. ] May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and Categorization Tool (RACT) . Reviews the study scope of work, budget and protocol content and ensures the clinical project team (CRAs/ Central Monitors) is aware of the contractual obligations and parameters. Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. Escalates to the project manager any risks to clinical [. .. ]
Job am 25.04.2026 bei Jooble gefunden
Biontech
Manager Statistical Programming
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
As
Manager Statistical Programming you will be responsible for working collaboratively with
Clinical Development team or CRO to meet project deliverables and timelines for statistical data analysis and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] reporting, you will independently perform or oversees the production and/or validation of programming deliverables (e. g. , analysis datasets, tables, listings) for study reports and integrated summaries. Your main responsibilities are: Works collaboratively with Clinical Development team or CRO to meet project deliverables and timelines for statistical data analysis and reporting Independently performs or oversees the production and/or validation of programming deliverables (e. g. , analysis datasets, tables, listings) for study reports [. .. ]
Job am 24.04.2026 bei Jooble gefunden
Global Study Manager ( Project Manager) - Sponsor-dedicated, in EMEA
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
Global
Study Manager ( Project Manager) - Sponsor-dedicated, in EMEA Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem [. .. ]
Job am 23.04.2026 bei Jooble gefunden
Eurofins
Senior Study Director/ Senior Study Manager Analytical Chemistry (m/f/d) - Scientist/ Chemist for Environmental
• Enzkreis; Region Nordschwarzwald, Württemberg; Regierungsbezirk Karlsruhe; Württemberg Niefern- Öschelbronn, DE
Führungs-/ Leitungspositionen
Work-Life-Balance
[. .. ] group and offers analytical studies to support the testing, development, and registration of test substances worldwide. To strengthen our Environmental Fate Metabolism department, we are looking for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a committed Senior Study Director/ Senior Study Manager. Environmental Fate Metabolism: 14C-labeled environmental fate studies in water, soil, and air Metabolism studies in plants and animals Leaching, persistence, and bioaccumulation studies Job Description You will contribute to improved environmental safety by conducting studies according to international guidelines (such as OECD, SANTE, EPA) . In close cooperation with [. .. ] portfolio of more than 200, 000 analytical methods to assess the safety, identity, composition, authenticity, origin, traceability, and purity of biological substances and products, as well as innovative services in clinical diagnostics, making it one of the world s leading emerging providers of specialized clinical diagnostic tests. In 2025, Eurofins achieved total revenues of 6.515 billion and has been one of the best-performing stocks in Europe over the past 20 years. We support your development Do you feel you [. .. ]
Job am 22.04.2026 bei Jooble gefunden
PSI CRO
Central Monitoring Manager
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
[. .. ] moving forward, the central monitoring function has become a top priority at PSI. We are looking for a person, who would lead the risk-based monitoring approach implementation [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on the clinical study and program level to ensure patient safety and data integrity. You will: Lead and facilitate initial and ongoing study Risk Management Participate in selection and setup of the RBM platform Perform Centralized Monitoring for a study including review of Key Risk Indicators, Statistical Analyses and Quality Tolerance Limits Present Centralized [. .. ] Communicate study challenges to Clinical Data Science group and work out data-driven solutions Qualifications College/ University degree or an equivalent combination of education, training and experience Clinical Study Lead/Manager experience Strong communication presentation skills are essential Leadership and ability to work independently are essential Centralized Monitoring experience is a plus Critical thinking and analytical skills Ability to work with complex data and provide insight into risk reports and trends Ability to adapt to changing circumstances and learn quickly Knowledge [. .. ]
Job am 21.04.2026 bei Jooble gefunden
Neo Carbon
Project Manager (m/f/d)
• Regierungsbezirk Kassel; Hessen Kassel, DE
[. .. ] on a regular basis and as needed Literature research Education/ Qualification Requirements: Ph D in natural sciences or Master degree in natural sciences with at least two [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] years of experience in clinical study project management Several years of professional experience (know how) in biomedical research and in mentoring of clinical trials would be a plus Experience in project management Communication and negotiation skills Good English and German skills Team player 89254339 [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Study Manager pro Jahr?
Als Clinical Study Manager verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Study Manager Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 130 offene Stellenanzeigen für Clinical Study Manager Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Study Manager Jobs?
Aktuell suchen 26 Unternehmen nach Bewerbern für Clinical Study Manager Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Study Manager Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Study Manager Stellenangebote:
- Biontech (5 Jobs)
- Thermo Fisher Scientific (4 Jobs)
- SCARLETRED Holding GmbH (3 Jobs)
- ICON (3 Jobs)
- Herman Medical Staffing GmbH (3 Jobs)
- PSI CRO (2 Jobs)
In welchen Bundesländern werden die meisten Clinical Study Manager Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Study Manager Jobs werden derzeit in Bayern (39 Jobs), Berlin (15 Jobs) und Niedersachsen (11 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Study Manager Jobs?
Clinical Study Manager Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
