ProRelix Research is a globally recognized Contract Research Organization (CRO) dedicated to advancing clinical trials and drug development. With a commitment to innovation, integrity, and patient-centric research, we partner with pharmaceutical and biotech companies to deliver high-quality clinical data. Our team thrives in a fast-paced, collaborative environment, making a real impact on global healthcare.
Detailed Job Openings
1. Clinical Research Associate – I (CRA-I)
Experience: 1+ years in clinical research
Responsibilities:
- Conduct site monitoring visits (PSV, SIV, RMV, COV)
- Ensure protocol & regulatory compliance
- Review case report forms (CRFs) & source documents
- Support site staff in trial execution
2. Clinical Research Associate – II (CRA-II)
Experience: 2–3 years in monitoring
Responsibilities:
- Lead site management & training
- Perform risk-based monitoring
- Resolve data discrepancies & protocol deviations
- Liaise with sponsors & investigators
3. Clinical Trial Assistant – I (CTA-I)
Experience: 0–6 months (Freshers welcome!)
Responsibilities:
- Assist in trial documentation & TMF maintenance
- Coordinate investigator meetings
- Track study progress & site communications
4. Clinical Data Management – Manager
Experience: 8+ years in CDM
Responsibilities:
- Oversee data validation & cleaning
- Lead EDC development & database lock
- Ensure compliance with CDISC, SDTM, & 21 CFR Part 11
- Mentor junior data managers
Eligibility & Skills
✔ Degree in Life Sciences, Pharmacy, or Medicine
✔ Strong knowledge of ICH-GCP, FDA/EMA guidelines
✔ For CRAs: Willingness to travel (50-70%)
✔ For CDM: SAS, Medidata Rave, or Oracle Clinical expertise
Why Join ProRelix?
✅ Competitive salary & performance bonuses
✅ Flexible work options (Hybrid/Remote for some roles)
✅ Continuous learning & career growth
✅ Work on global trials with top pharma sponsors
How to Apply?
📩 Email your resume to: career@prorelixresearch.com
