13 beste Stellen als clinical research associate in münchen – aktuell auf Personalsuche

Clinical Research Associate I (CRA I) / Klinischer Monitor – Full-Time or Part-Time Available (m/w/d)
Thermo Fisher Scientific —München
- Vollzeit
- Englisch
- Microsoft Office
- Präsentationserfahrung
2 Tage
Clinical Research Associate / Senior CRA
Edwards Lifesciences —Garching bei München
- Vollzeit
- Englisch
- Forschungserfahrung
- Microsoft Office
- Kostenbeteiligung am Arbeitsweg
- Flexible Arbeitszeiten
Clinical Research Associate based in Germany
Fortrea —München
- Vollzeit
- Nursing
- Management-Erfahrung
- Mit Reiseanteil
Clinical Research Associate - Germany
Linical —München
- Hybrides Arbeiten
- Management-Erfahrung
- Englisch
- Forschungserfahrung
Clinical Development Associate (m/f/d)
VeonGen Therapeutics GmbH —Planegg
- Forschungserfahrung
- Mit Reiseanteil
Clinical Research Associate / Senior Clinical Research Associate
PSI CRO —München
- Vollzeit
- Hybrides Arbeiten
- Englisch
- Microsoft Office
- Mit Reiseanteil
Direkt bewerben
Study Start Up Associate
Alira Health —München
- Vollzeit
- Microsoft Office
- Bachelor
Senior Clinical Research Associate (w/m/d) - sponsor dedicated - home based
Fortrea —München
- Vollzeit
- Englisch
- Forschungserfahrung
- Organisationstalent
- Weiterbildungsprogramme
- Flexible Arbeitszeiten
Senior Clinical Research Associate
Veranex, Inc. —München
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Direkt bewerben
(Junior) Clinical Trials Manager - Site Management und Monitoring Oversight
FUTRUE —Gräfelfing
- 52.000 € – 71.800 € pro Jahr
- Vollzeit
- Englisch
- Organisationstalent
- Kommunikationsfähigkeit
Direkt bewerben
Senior CRA II Sponsor Dedicated based in Düsseldorf region
Fortrea —München
- Vollzeit
- Forschungserfahrung
- Bachelor
- Ohne Hochschulabschluss
Associate Director (m/f/d), Computational Pathology Biomarker Lead (Oncology/BioPharma)
AstraZeneca —München
- Doktorat
- Künstliche Intelligenz
- Python
- Aufstiegsmöglichkeiten
Senior CRA
Alira Health —München
- Vollzeit
- Management-Erfahrung
- Kundenberatung
- Forschungserfahrung

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Senior Clinical Trial Coordinator
Alira Health —München
Previous experience in clinical research (in CROs, Pharma or academy/hospital experience). The Senior Clinical Trial Coordinator assists the clinical research…
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Clinical Research Associate - Germany
Linical —München
Excellent understanding of the clinical research process, clinical trial-related systems and procedures, regulations and GCPs, and the scientific/clinical…

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Clinical Research Associate I (CRA I) / Klinischer Monitor – Full-Time or Part-Time Available (m/w/d)

Thermo Fisher Scientific -
München

Jetzt bewerben

Details zur Stelle

Vollzeit
vor 2 Tagen

Qualifikationen

Prozessverbesserung
Englisch
Microsoft Office
Präsentationserfahrung
Bachelor
Klinische Studien
PC-Kenntnisse
Medizinische Fachbegriffe
Deutsch
Zeitmanagement

Vollständige Stellenbeschreibung

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and 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 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 future.

Our clinical department defines, develops and delivers clinical programmes. Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and implement high-quality, cost-efficient clinical studies.

The role can be home-based, office-based in Munich or Karlsruhe, or hybrid, and is offered as a permanent full time (1 FTE) or part-time position (0.8 FTE / 80%).

The CRA:

Performs and coordinates all aspects of the clinical monitoring and site management process.
Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation..
Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability.
Ensures audit readiness.
Develops collaborative relationships with investigational sites.
Detailed tasks and responsibilities assigned to role are outlined in the task matrix.
Travel up to 50-75%

A day in the Life:

Monitors investigator sites with a risk-based monitoring approach applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks.
Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities.
Assess investigational product through physical inventory and records review.
Documents observations in reports and letters in a timely manner using approved business writing standards.
Brings up observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution.
May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
Conducts monitoring tasks in accordance with the approved monitoring plan.
Participates in the investigator payment process.
Ensures a shared responsibility with other project team members on issues/findings resolution.
Investigates and follows-up on findings as applicable
Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required.
Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS).
Performs QC check of reports generated from CTMS system where required.
Participates in investigator meetings as necessary.
Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures trial close out and retrieval of trial materials.
Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.
Gives to the project team by assisting in preparation of project publications/tools and sharing ideas/suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc).
Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.
Responds to company, client and applicable regulatory requirements/audits/inspections.
Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.
Gives to other project work and initiatives for process improvement, as required.

Education and Experience

Bachelor's degree in a life sciences related field or equivalent and relevant formal academic / vocational qualification.
Previous experience in a clinical environment with exposure to clinical research, healthcare or clinical trials that provides the knowledge and skills required to perform the role
Valid driver's license
Full Right to work in Germany
Fluency in English and German language to at least C1 level (note that the interview will be held in German).

Knowledge, Skills, Abilities

Effective clinical monitoring skills
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Excellent understanding and demonstrated application of ICH GCPs, applicable regulations and procedural documents
Well-developed critical thinking skills, including but not limited to: critical attitude, in-depth investigation for appropriate root cause analysis and decision-making
Ability to handles Risk Based Monitoring concepts and processes
Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues
Effective social skills
Strong attention to detail
Effective organizational and time management skills
Ability to remain flexible and adaptable in a wide range of scenarios
Ability to work in a team or independently as required
Good computer skills: proficient knowledge of Microsoft Office and the ability to learn appropriate software
Good presentation skills

Severely disabled applicants with the same aptitude will be given preferential treatment. / Schwerbehinderte Bewerber werden bei gleicher Eignung bevorzugt behandelt.

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Erweiterte Suche

clinical research associate Jobs in münchen

Clinical Research Associate I (CRA I) / Klinischer Monitor – Full-Time or Part-Time Available (m/w/d)

Clinical Research Associate / Senior CRA

Clinical Research Associate based in Germany

Clinical Research Associate - Germany

Clinical Development Associate (m/f/d)

Clinical Research Associate / Senior Clinical Research Associate

Study Start Up Associate

Senior Clinical Research Associate (w/m/d) - sponsor dedicated - home based

Senior Clinical Research Associate

(Junior) Clinical Trials Manager - Site Management und Monitoring Oversight

Senior CRA II Sponsor Dedicated based in Düsseldorf region

Associate Director (m/f/d), Computational Pathology Biomarker Lead (Oncology/BioPharma)

Senior CRA

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