Aktuelle Jobs im Zusammenhang mit CRA- Germany - Deutschland - Barrington James
-
Senior Information Security Management Systems
vor 3 Wochen
Deutschland RED Global VollzeitHIRING Information Security Management Systems (ISMS) Manager Level - Senior Location: GERMANY ( Onsite Presence Required) Technology-Skill - Security Frameworks Language: German (Mandatory) If you're interested, please directly forward your CV to me at jkhan@redglobal.com About the Role We are seeking a Senior Information Security Management Systems (ISMS)...
-
Senior Clinical Research Associate
vor 3 Wochen
Deutschland AL Solutions VollzeitSenior Clinical Research Associate – Germany (Home-Based, French Speaking) Chloe O’Shea is pleased to be working with a small global CRO recognised for driving innovation and excellence in clinical development. We are seeking an experienced Clinical Research Associate to join a sponsor-dedicated team, home-based in Germany. This is a unique opportunity...
-
Senior Clinical Research Associate
Vor 2 Tagen
Deutschland Planet Pharma VollzeitSenior CRA – Germany Therapeutic Area: Cell & Gene Therapy Location: Germany Freelance contract (min 0.8 FTE) About the Role We are seeking an experienced Senior Clinical Research Associate to join an innovative, fast-growing biopharmaceutical organisation advancing next-generation cell and gene therapies . You will play a key role in overseeing complex...
CRA- Germany
vor 4 Wochen
Freelance Clinical Research Associate- Part-Time Hours: Approx. 4 hours per week Start Date: ASAP Study: Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) I am seeking a Clinical Research Associate (CRA) with strong Real World Evidence Ethics Submissions experience for a part-time role based in Germany . The successful candidate will play a key role in supporting the set-up, initiation, and ongoing management of study sites for a review study in Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) . Key Responsibilities: Site Contracting: Manage the contracting process with study sites. Training & Support: Provide training to site staff on study procedures and requirements. Ethical and Compliance Advice: Ensure sites adhere to ethical and regulatory standards. Ethics Applications & Approvals: Prepare and submit applications for ethics committee review, ensuring local site approvals are secured. Data Query Management: Address data queries and ensure data quality. Regulatory Support: Assist sites with regulatory requirements. Ongoing Site Management: Oversee and support site performance throughout the study. Stakeholder Communication: Maintain regular communication with site staff, study team, and other relevant stakeholders. Key Requirements: Proven experience as a Clinical Research Associate (CRA) Solid understanding of clinical trial processes, ethics committees, and regulatory requirements. Experience with retrospective chart review studies is a plus. Fluent in both German and English (both written and spoken). Availability to commit to approximately 4 hours per week , starting ASAP. If you're an experienced Clinical Research Associate with RWE Ethics Submission experience and 4 hours per week available, we would love to hear from you To apply , please submit your CV here directly.
