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Medpace Hiring For Clinical Safety, Pharmacovigilance, Medical Writing, Data Management, and Programming, SAS Programmer

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Medpace, a globally recognized Contract Research Organization (CRO), is expanding its India operations and hiring for 8 key positions in Navi Mumbai across Clinical Safety, Pharmacovigilance, Medical Writing, Data Management, Core Laboratory, and Programming functions.

This recruitment drive is an excellent opportunity for pharmacy, life science, nursing, biomedical, and data professionals seeking long-term career growth in the clinical research industry.

With over 30+ years of global CRO experience, Medpace offers structured career paths, competitive compensation, and exposure to international clinical trials across oncology, cardiology, CNS, infectious diseases, and more.

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๐Ÿ“Œ Open Positions at Medpace (Navi Mumbai)

1๏ธโƒฃ Safety Database Specialist โ€“ Clinical Safety

Experience: 1โ€“2 years
Key Skills: Argus, Argus J, SQL, OBIEE, UAT, Safety Reports (DSUR, PSUR, PBRER)

Responsibilities

  • Configure studies, products, and licenses in Argus
  • Generate safety reports and analytics
  • Perform UAT and resolve database issues
  • Support audits, inspections, SOPs, and training

2๏ธโƒฃ Drug Safety Specialist / Clinical Safety Coordinator

Preferred Background: Nursing, Pharmacy, Life Sciences

Responsibilities

  • Process AE/SAE cases
  • Write safety narratives
  • Collaborate with clinical sites
  • Support post-marketing pharmacovigilance

3๏ธโƒฃ Medical Writer โ€“ Core Labs

Qualification: Masterโ€™s in Health or Science

Responsibilities

  • Develop and QC clinical documents
  • Maintain audit trails
  • Support data analysis planning

4๏ธโƒฃ Project Coordinator โ€“ Core Laboratory (Imaging)

Qualification: Biomedical Engineering (Bachelorโ€™s/Masterโ€™s)

Responsibilities

  • Manage imaging study timelines
  • Coordinate with sites and internal teams
  • Maintain imaging inventory

5๏ธโƒฃ Database Programmer โ€“ Data Management

Skills: SQL, C#, Clinical Databases

Responsibilities

  • Develop and validate clinical databases
  • Design eCRFs and edit checks
  • Provide technical support to DM teams

6๏ธโƒฃ Data Coordinator โ€“ Core Laboratory

Experience: 1โ€“2 years preferred

Responsibilities

  • Data validation and cleanup
  • Prepare DM documents
  • Handle external data transfers

7๏ธโƒฃ Data Coordinator โ€“ Data Management

Skills: Medidata RAVE, Clinical Data Cleaning

Responsibilities

  • Track EDC metrics
  • Resolve data queries
  • Reconcile clinical data

8๏ธโƒฃ SAS Programmer โ€“ Core Laboratory

Requirement: SAS Certification

Responsibilities

  • Program and validate mapped databases
  • Prepare data transfer specifications
  • Coordinate with Data Management teams

๐ŸŽ“ Eligibility & Qualifications (Summary)

  • Degrees: B.Pharm, M.Pharm, MSc, Nursing, Biomedical, Life Sciences, IT, Math, Statistics
  • Freshers to 1โ€“2 years experience for most roles
  • Strong knowledge of clinical research, pharmacovigilance, databases, or programming
  • Excellent communication and attention to detail

๐Ÿ’ผ Why Join Medpace?

  • Flexible work environment
  • Competitive salary & benefits
  • Structured career growth paths
  • Global exposure to Phase Iโ€“IV trials
  • Employee wellness initiatives
  • Forbes-recognized CRO (2021โ€“2024)

๐Ÿ’ฐ Estimated Salary Range (India)

  • โ‚น4.5 LPA โ€“ โ‚น10 LPA (depending on role, skills, and experience)

๐Ÿ“ How to Apply

Application Link for Safety Database Specialist โ€“ Clinical Safety

Application Link for Drug Safety Specialist / Clinical Safety Coordinator

Application Link for Medical Writer โ€“ Core Labs

Application Link for Project Coordinator โ€“ Core Laboratory (Imaging)

Application Link for Database Programmer โ€“ Data Management

Application Link for Data Coordinator โ€“ Core Laboratory

Application Link for Data Coordinator โ€“ Data Management

Application Link for SAS Programmer โ€“ Core Laboratory

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