Senior Clinical Research Associate (CRA) – Germany
Job Highlights & Employer Insights
Kolkata VerifiedResponse Rate
94% High Response
Recruiter actively reviews profiles
Avg. Turnaround
3–5 Days
Fast shortlist & interview calls
Verified Employer
Official Partner
Direct listing from CTI
Culture Score
4.8 ★ Rating
Great feedback from current team
Job Overview
Experience
3-5
Salary
Best in Industry
Openings
Multiple Openings
Employment Type
full_time
Work Mode
On-site
Shift
Day Shift
Working Days
Monday to Saturday
Notice Period
Immediate to 30 Days
Education
Graduate
Job Category
ICH GCP
Job Summary
CTI is seeking an experienced Clinical Research Associate to serve as the primary contact for assigned study sites in Germany. The role involves conducting site visits—from pre‑study to close‑out—ensuring all deliverables meet quality standards and timelines while adhering to ICH‑GCP and regulatory requirements. Responsibilities include site start‑up, document review, training, enrollment strategy, investigational product management, and remote monitoring. Candidates will collaborate closely with the Clinical Project Manager and project team, providing ongoing status updates and participating in investigator and client meetings. The position requires strong knowledge of regulatory frameworks, excellent German and English communication skills, and a background in life sciences. CTI offers a supportive, growth‑focused environment with mentoring, leadership development, and hybrid work options. The role is full‑time, requires 3–5 years of CRA experience in Germany, and focuses on advancing patient‑centered medicine.
Key Responsibilities
- CTI is seeking an experienced Clinical Research Associate to serve as the primary contact for assigned study sites in Germany. The role involves conducting site visits—from pre‑study to close‑out—ensuring all deliverables meet quality standards and timelines while adhering to ICH‑GCP and regulatory requirements. Responsibilities include site start‑up, document review, training, enrollment strategy, investigational product management, and remote monitoring. Candidates will collaborate closely with the Clinical Project Manager and project team, providing ongoing status updates and participating in investigator and client meetings. The position requires strong knowledge of regulatory frameworks, excellent German and English communication skills, and a background in life sciences. CTI offers a supportive, growth‑focused environment with mentoring, leadership development, and hybrid work options. The role is full‑time, requires 3–5 years of CRA experience in Germany, and focuses on advancing patient‑centered medicine.
About the Role
This role is ideal for someone who enjoys combining strategy, content, data and execution. You will work with cross-functional teams and contribute directly to the company’s digital growth in Kolkata and surrounding areas.
Job Requirements
- ICH GCP
- Clinical Monitoring
Required Skills
Education
Bachelor's Degree
Preferred Languages
English, Hindi, Bengali
Gender / Eligibility
Any
Age Limit
Not Applicable
Benefits & Perks
Hiring Process Timeline
Transparent recruitment steps for this position
Submit CV & Application
Quick 1-step resume submission on OurKolkata
Recruiter Review
CTI hiring team evaluates candidate profile
Interview Rounds
Personal or online interview with department heads
Job Offer & Joining
Official offer letter issuance and onboarding
About the Company
CTI
CTI is a leading organization in Kolkata delivering high-value products and professional services.
Industry
Technology & Services
Company Size
100–500 Employees
Founded
2005
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Senior Clinical Research Associate (CRA) – Germany
Best in Industry
