Job Opportunity: Senior Clinical Data Associate – Ahmedabad
Job Summary
Advanced Clinical is seeking a detail-oriented and experienced Senior Clinical Data Associate to join our growing team in Ahmedabad. This role offers a unique opportunity to work within a global clinical research organization, managing high-impact clinical trials. The successful candidate will play a pivotal role in ensuring the integrity, accuracy, and regulatory compliance of clinical data throughout the end-to-end trial lifecycle. If you have a passion for clinical research, possess strong analytical skills, and are ready to advance your career in a dynamic, innovation-driven environment, we invite you to apply.
Responsibilities
As a Senior Clinical Data Associate, you will be responsible for overseeing critical data management activities. Your core duties will include:
- Data Review and Validation: Conduct comprehensive data reviews for ongoing clinical trials to ensure complete, accurate, and high-quality data.
- eCRF Management: Monitor electronic Case Report Forms (eCRFs) to ensure consistency and adherence to study protocols.
- Query Resolution: Proactively generate, track, and resolve manual queries to maintain data cleanliness.
- Reconciliation: Manage complex SAE (Serious Adverse Event) reconciliation and ensure alignment between vendor data and the clinical database.
- Documentation and Planning: Assist in the creation and maintenance of Data Management Plans (DMP), edit checks, and data listing specifications.
- System Testing: Perform User Acceptance Testing (UAT) for various clinical systems to ensure functionality meets project requirements.
- EDC Support: Support integration tasks for EDC systems, including ePRO, randomization, and dispensing modules.
- Trend Analysis: Identify data discrepancies and emerging trends, escalating issues as necessary to ensure project timelines remain on track.
- Administrative Oversight: Manage user access permissions, compile study metrics reports, and execute quality control (QC) reviews and EDC archival procedures.
- Compliance: Maintain strict adherence to internal Standard Operating Procedures (SOPs) and global regulatory standards.
Requirements
To be successful in this role, you must meet the following qualifications:
- Experience: A minimum of 3 years of professional experience in Clinical Data Management, specifically within a CRO or pharmaceutical setting.
- Technical Proficiency: Strong working knowledge of EDC systems, eCRFs, and clinical database architectures.
- Standards Knowledge: Demonstrated expertise in CDASH standards.
- Analytical Skills: Solid understanding of clinical workflows, including SAE reconciliation processes.
- Education: A Bachelor’s degree in a relevant field (or equivalent professional experience).
- Soft Skills: Excellent communication, organizational, and critical thinking skills, with the ability to manage multiple priorities in a fast-paced global environment.
Why Join Advanced Clinical?
Advanced Clinical is dedicated to improving patient outcomes through excellence in clinical research. We foster an inclusive and diverse workplace that prioritizes innovation, data integrity, and compliance. By joining our team, you will:
- Gain exposure to the full lifecycle of global clinical trials.
- Work within a collaborative culture that values professional development and career progression.
- Contribute to high-quality clinical research that prioritizes patient safety.
Salary & Benefits
We offer a competitive compensation package commensurate with experience:
- Estimated Salary: ₹6,00,000 – ₹10,00,000 per annum.
- Growth: Significant opportunities for career advancement in clinical research and data science.
- Environment: A supportive, global team environment that encourages innovation and teamwork.
How to Apply
If you are ready to take the next step in your career and contribute to life-changing clinical research, please submit your application through the official portal provided below.
Click here to apply for the Senior Clinical Data Associate position
Advanced Clinical is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
