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Torrent Pharmaceuticals Hiring Clinical Operations Executive

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Torrent Pharmaceuticals

M.Pharm / Pharm.D

Ahmedabad & Gandhinagar

3–8 years

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Torrent Pharmaceuticals is hiring Clinical Operations Executives for its Research & Development team in Ahmedabad and Gandhinagar. The role involves clinical study start-up, site management, clinical trial monitoring, vendor coordination, clinical trial supplies, and project management.

Job Details

DetailsInformation
CompanyTorrent Pharmaceuticals
PositionClinical Operations Executive
LocationAhmedabad, Gandhinagar
Experience3–8 years
Openings2
Employment TypeFull Time, Permanent
DepartmentResearch & Development
IndustryPharmaceutical & Life Sciences
QualificationM.Pharm / Pharm.D
Relevant ExperienceCRA experience
Travel RequirementWillingness to travel 20–25 days per month

Position

Clinical Operations Executive

The Clinical Operations Executive will support clinical studies across study start-up, site management, clinical study monitoring, clinical trial supplies, vendor management, and project management.

Key Responsibilities

Study Start-Up

  • Conduct site feasibility assessments.
  • Perform site evaluation and selection.
  • Manage site/investigator financial and study contract execution.
  • Prepare Ethics Committee (EC) submission packages.

Site Management & Clinical Study Monitoring

  • Support site initiation and liaisoning.
  • Conduct site staff training and re-training.
  • Oversee patient recruitment and retention.
  • Troubleshoot site recruitment issues.
  • Perform study monitoring.
  • Conduct source data verification and ensure data quality.
  • Support site audits.
  • Manage site close-out activities.

Clinical Trial Supplies

  • Manage clinical trial supplies.

Vendor Management

  • Coordinate and manage vendors involved in clinical studies.

Project Management

  • Track project timelines and budgets.
  • Manage site and vendor invoice payments.
  • Coordinate with cross-functional teams.

Eligibility and Qualifications

Education

  • M.Pharm
  • Pharm.D

Experience

  • 3–8 years of experience
  • Experience working as a Clinical Research Associate (CRA).

Other Requirement

  • Willingness to travel 20–25 days per month.

Required Skills

  • Regulatory understanding.
  • Clinical study monitoring.
  • Site management.
  • Site feasibility and selection.
  • Vendor coordination.
  • Project tracking.
  • Clinical trial supplies management.
  • Source data verification and data quality management.

Application Details

Application Link

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