Avance Clinical, a leading global Contract Research Organisation (CRO), is hiring a Clinical Data Associate in Bengaluru, Karnataka. This full-time, on-site position is ideal for candidates with 2–3 years of experience in clinical research, data management, and GCP environments.
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If you are detail-oriented, passionate about clinical trials, and looking to advance your career in the pharmaceutical industry, this role offers an excellent opportunity.
Key Responsibilities
As a Clinical Data Associate at Avance Clinical, you will:
- Develop and review Case Report Forms (CRFs) and completion guidelines.
- Prepare Data Management Plans and support edit check documentation.
- Validate databases using dummy data and SAS outputs.
- Perform data review, discrepancy resolution, and query management.
- Assist with MedDRA / WHO-DD coding under mentor guidance.
- Conduct quality control checks prior to database lock.
- Archive study documentation, including Medrio files.
- Support filing, reconciliation, and CRF tracking processes.
- Collaborate effectively with cross-functional teams.
Required Qualifications & Skills
- Bachelor’s degree in Life Sciences, Pharmacy, or related discipline.
- 2–3 years’ experience in CRO/pharmaceutical industry under GCP compliance.
- Strong knowledge of ICH-GCP guidelines, clinical trial processes, and medical terminology.
- Hands-on experience in data entry and discrepancy management.
- Excellent time management, communication, and organizational skills.
- Proficiency in MS Office Suite and ability to work independently.
Benefits of Joining Avance Clinical
- Opportunity to work with a globally recognized CRO.
- Exposure to innovative drug development projects.
- Supportive and collaborative work environment.
- Professional growth with training and mentorship.
How to Apply
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