Associate Clinical Data Specialist
📍 Location: Mumbai, Maharashtra, India
🕒 Type: Full-time
📅 Posted: 7 Days Ago
📄 Requisition ID: R50296
🏢 Company: Medtronic
About Medtronic
At Medtronic, you can begin a life-long career of exploration and innovation, helping champion healthcare access and equity for all. You’ll lead with purpose — breaking barriers to innovation in a more connected, compassionate world.
Position Summary
The Associate Clinical Data Specialist is responsible for supporting the design, documentation, testing, and implementation of clinical data collection systems and databases. The role collaborates cross-functionally to ensure data integrity, compliance, and efficiency in clinical studies.
Key Responsibilities
Collaborate with various departments in the design, documentation, testing, and implementation of clinical data collection studies.
Design and implement clinical protocols and data collection systems.
Develop systems to organize, analyze, identify, and report data and trends.
Manage data management issues by ensuring cross-project consistency and identifying standard Case Report Form (CRF) modules.
Develop and maintain data quality plans.
Provide strategic input into protocol design with a focus on data management.
Review and resolve data discrepancies using standardized validation systems and procedures.
Prepare clinical trial reports for internal validation and cross-validation studies.
Career Stream – Specialist
Role Type: Individual contributor (professional discipline or specialty).
Work Focus: Delivering and managing assigned projects, from design to implementation.
Mentorship: May mentor colleagues or guide lower-level professionals.
Supervision: Works under close supervision; autonomy increases with experience.
Differentiating Factors
|
Category |
Description |
|---|---|
|
Autonomy |
Entry-level contributor; works with close supervision. |
|
Organizational Impact |
Delivers work of limited scope; small or less complex projects. |
|
Innovation & Complexity |
Solves straightforward problems; may make minor process improvements. |
|
Communication & Influence |
Communicates mainly with internal team members; gathers and conveys information. |
|
Leadership |
No formal leadership; focuses on self-development. |
|
Knowledge Required |
Broad theoretical job knowledge gained through advanced education. |
Qualifications
Minimum 3+ years of experience in Clinical Data Management.
Strong understanding of clinical databases, CRF design, and data validation systems.
Excellent analytical, documentation, and communication skills.
Ability to work in a collaborative team environment and manage priorities effectively.
Physical Job Requirements
The responsibilities and physical demands described here represent the general nature and level of work expected of employees in this role. They are not exhaustive of all duties and skills required.
Compensation & Benefits
Competitive salary and flexible benefits package.
Medtronic Incentive Plan (MIP): Short-term performance-based incentive eligibility.
Comprehensive career and life-stage support, including wellness, insurance, and professional development programs.
Recognition and rewards for contributions to company success.
Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | surat | Tarasadi | Vadodara | Vapi |Maharashtra :
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Siliguri |Illinois :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Atlanta | Augusta | Rome |Maine :
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Copenhagen | Denmark |Europe :
Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
Finland |Istanbul :
Istanbul | Turkey |Norway :
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Sheffield |Oxfordshire :
Witney |Ontario :
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Montreal |Brussels :
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Zaventem |South America :
Peru | Argentina |Brazil :
Brazil | Sao paulo |Attica :
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Auckland |New Zealand :
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Manila |Croatia :
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Zagreb |Estonia :
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