At a Glance
- Tasks: Lead clinical research projects and ensure compliance with regulations while making a real impact.
- Company: Join an award-winning global team dedicated to advancing medicine.
- Benefits: Professional growth opportunities, hybrid work, and a supportive culture.
- Other info: Enjoy a balanced work-life with opportunities to give back to the community.
- Why this job: Make a difference in patients' lives by developing life-changing treatments.
- Qualifications: 3-5 years of clinical research experience and fluency in German and English.
The predicted salary is between 40500 - 49500 £ per year.
Serve as main CTI contact for assigned study sites.
Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP.
Assist with or oversee study start-up activities, including feasibility, pre-study activities and site selection.
Collect, review and track essential/regulatory documents.
Participate in and complete all general and study specific training as required.
Participate in investigator, client and project team meetings; may include presentations.
Create and implement subject enrollment strategies for assigned study sites.
Ensure proper storage, dispensation and accountability of all Investigational Product (IP) and trial-related materials.
Perform site management activities and provide ongoing updates of site status to Clinical Project Manager.
Conduct remote monitoring and complete related activities in accordance with study specific Monitoring Plan.
Utilize systems and reports to track subject status, subject case report form (CRF) retrieval / source document review (SDV), regulatory documents, and IP.
Assist with project-specific activities as member of Project Team.
What You'll Bring:
- 3 - 5 years clinical research experience as a CRA or related profession in Germany incl. independent monitoring experience in Germany.
- Life science background.
- Excellent knowledge in ICH-GCP and regulatory requirement.
- Fluent (at least Level B2) in spoken and written language German and English.
About CTI:
Advance Your Career – We invest in your professional growth. Our structured mentoring program, leadership development courses, and dedicated training department provide the support you need to excel. We also encourage ongoing education to help you achieve your professional goals.
Join an Award-Winning Team – Join a global team spanning 60 countries, recognized for its award-winning culture that prioritises people. We support your work-life balance with hybrid work opportunities. Through our CTI Cares program, you’ll have opportunities to give back to your community and the world.
Make a Lasting Impact – At CTI, your work directly contributes to advancing medicine. You’ll play a vital role in developing life-changing treatments for patients with chronic and critical illnesses. Together, we move medicine forward, making a difference for those who need it most.
Please Note: We will never communicate with you via Microsoft Teams or text message. We will never ask for your bank account information at any point during the recruitment process.
Clinical Research Associate II / Senior Clinical Research (level dependent on experience) employer: Ctifacts
CTI is an exceptional employer that prioritises professional growth and work-life balance, offering structured mentoring programs and leadership development courses to support your career advancement. With a global presence across 60 countries, our award-winning culture fosters collaboration and community engagement through initiatives like CTICares, allowing you to make a meaningful impact in the field of medicine while enjoying the flexibility of remote work.
