We are looking for a detail-oriented and responsible Data Entry Operator to support our clinical research study team with study data management, patient follow-up coordination, and documentation.

Key Responsibilities:

- Study Data Entry
- Enter patient and study-related information from source documents and Case Report Forms (CRFs) into the designated study database.
- Ensure accuracy, completeness, and timely updating of study records.
- Update patient records based on information received during follow-ups.
- Patient Follow-up Coordination
- Coordinate with enrolled patients for scheduled study visits and follow-ups.
- Make follow-up calls and reminders as per study requirements.
- Collect and document relevant follow-up information and communicate updates to the study team.
- Data Documentation & Tracking
- Maintain patient follow-up records and visit status.
- Track missing, incomplete, and pending data.




- Assist in reconciliation and updating of study records.
- Confidentiality & Data Protection
- Maintain strict confidentiality of patient information and study-related documents.
- Ensure appropriate handling and protection of sensitive study data.

- General Study Support
- Provide administrative and data-related assistance to the study team.
- Support the Principal Investigator and study team in maintaining accurate and complete study documentation.

Desired Skills:

- Good typing and data entry skills.
- Basic knowledge of MS Excel and MS Office.
- Positive communication and coordination skills.
- Attention to detail and accuracy.
- Ability to maintain confidentiality of patient information.
- Prior experience in clinical research or healthcare data entry will be an added advantage.

📌 Data Entry Operator (New Delhi)
🏢 Wembrace Biopharma
📍 New Delhi