Associate Clinical Data Specialist
Location: Remote – Chennai Kilpauk, Tamil Nadu, India
Employment Type: Full-time
Job Requisition ID: R55390
About Medtronic
Medtronic is a global leader in healthcare technology, dedicated to improving access, equity, and outcomes for patients worldwide. Our mission—to alleviate pain, restore health, and extend life—drives innovation across medical devices, clinical research, and patient care solutions. With a global team of over 95,000 professionals, we combine scientific expertise, engineering innovation, and compassionate care to tackle some of the most challenging health problems facing humanity.
Joining Medtronic means becoming part of a dynamic, mission-driven organization that values collaboration, inclusion, and career growth.
Role Overview
The Associate Clinical Data Specialist (ACDS) is responsible for the design, implementation, and oversight of clinical data collection studies and database management activities. This role ensures data accuracy, consistency, and integrity across clinical trials while collaborating with cross-functional teams to optimize study protocols and CRF design.
This position is ideal for early-career professionals seeking to build expertise in clinical data management within a global, regulated environment.
Key Responsibilities
Collaborate with clinical, data management, and statistical teams to design, document, and implement clinical data collection systems.
Develop, configure, and maintain Case Report Forms (CRFs) and standardized CRF modules across studies.
Monitor, review, and resolve data discrepancies using validated data management systems.
Support early-stage protocol design by providing data management strategic input.
Develop and implement data quality plans to ensure consistent, high-quality clinical data.
Analyze data trends and generate reports for internal validation, cross-validation, and clinical study review.
Contribute to project deliverables from study design to implementation, adhering to regulatory and company SOPs.
Participate in training, mentorship, and guidance of junior team members as required.
Differentiating Factors
Autonomy: Entry-level individual contributor with structured supervision and guidance.
Organizational Impact: Supports projects of limited scope, typically smaller clinical studies or sub-projects.
Innovation and Complexity: Identifies minor process improvements and problem resolution strategies within established frameworks.
Communication: Collaborates primarily with internal teams to gather, validate, and communicate study-related data and insights.
Leadership: Focused on self-development and building technical expertise in clinical data management.
Required Qualifications and Experience
Education
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field.
Equivalent international degrees are acceptable.
Experience
0–2 years of clinical data management or research experience preferred.
Exposure to clinical trial protocols, CRF design, or clinical database systems is a plus.
Knowledge and Skills
Strong analytical and problem-solving abilities.
Understanding of clinical research processes and regulatory requirements.
Ability to manage multiple tasks in a structured, detail-oriented manner.
Strong written and verbal communication skills in English.
Proficiency with standard office software; familiarity with EDC/CTMS platforms is an advantage.
Work Environment and Benefits
Remote work flexibility based in Chennai Kilpauk, Tamil Nadu.
Competitive salary with Medtronic Incentive Plan (MIP) eligibility.
Comprehensive benefits package including health, wellness, and career development support.
Opportunities for professional growth in a global, innovation-driven environment.
Why Join Medtronic
Medtronic empowers employees to explore, innovate, and drive meaningful impact in global healthcare. You will collaborate with a diverse team, work on cutting-edge clinical research initiatives, and contribute to technologies that improve patient lives worldwide.
Apply Now
Start your career in clinical data management at Medtronic and help shape the future of global healthcare while building expertise in clinical trials, data systems, and protocol design.
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