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.

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

Application Link