Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Clinical Studies Spt Coord Ii

Medtronic
Medtronic
2+ years
Not Disclosed
10 Jan. 19, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Studies Support Coordinator II
Location: Mumbai, Maharashtra, India (Remote Work Option Available)
Employment Type: Full-Time
Job ID: R55535
Posted: 26 Days Ago

About the Role
Medtronic is seeking a Clinical Studies Support Coordinator II to provide critical support for clinical studies, ensuring data integrity, regulatory compliance, and smooth operational processes. This role is ideal for professionals with experience in clinical study coordination, document management, and data verification within the healthcare or medical device industry.

Key Responsibilities

  • Support clinical studies by managing one or more operational areas, including:

    • Data Coordination: Participate in the development and testing of case report forms, study databases, and study reports in accordance with protocol requirements. Verify study data, resolve discrepancies, and ensure timely completion of data forms.

    • Document Coordination: Create, manage, and organize clinical study files. Maintain proper distribution and oversight of clinical study documents. Conduct periodic audits to ensure completeness and accuracy.

    • Compensation Processing: Identify and resolve compensation discrepancies where applicable.

  • Apply prior experience to routine administrative and clerical tasks while making minor adjustments to improve processes.

  • Communicate effectively with internal stakeholders across teams, providing explanations and interpretations of study procedures and data.

  • Provide guidance and support to new or entry-level team members.

  • Highlight areas of concern and propose solutions to enhance efficiency within assigned responsibilities.

Experience and Skills Required

  • Minimum 2 years of relevant experience in clinical study support, data coordination, or document management in the medical device, healthcare, or clinical research industry.

  • Strong knowledge of clinical study procedures, regulatory standards, and documentation requirements.

  • Ability to manage multiple tasks efficiently with moderate supervision.

  • Proficient in data verification, discrepancy resolution, and study file audits.

  • Excellent communication skills and ability to collaborate across teams.

  • Prior experience providing guidance to junior staff is preferred.

Education

  • Bachelor’s degree in Life Sciences, Clinical Research, Healthcare Administration, or related field is required.

Benefits & Compensation
Medtronic offers a competitive salary and flexible benefits package designed to support employees at every stage of their career. This position is eligible for the Medtronic Incentive Plan (MIP).

About Medtronic
Medtronic leads global healthcare technology and addresses critical health challenges worldwide. Our mission—to alleviate pain, restore health, and extend life—drives a diverse team of 95,000+ professionals who innovate across R&D, production, and clinical practice. We are committed to engineering real-world solutions while fostering a culture of inclusion, collaboration, and continuous improvement.

How to Apply
Join Medtronic and contribute to advancing clinical research with precision, compliance, and efficiency. Apply today to be part of a global team dedicated to healthcare innovation.