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Clinical Research Associate (CRA) Entry Jobs at Medpace | Freshers

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Medpace

B.Pharm, Pharm.D, M.Pharm, Biotechnology, Microbiology, Nursing, Physiotherapy, Biomedical Sciences, Clinical Research, Pharmacy Technician

Navi Mumbai

0 - 2 Years

Verified Job

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If you are looking to start a career in Clinical Research, Clinical Trials, or the CRO industry, Medpace Clinical Research India has opened applications for Clinical Research Associate (CRA) Entry positions in Navi Mumbai.

This opportunity is ideal for B.Pharm, M.Pharm, Pharm.D, Life Science, Biotechnology, Nursing, Pharmacy Technician, Research Assistant, and other healthcare graduates who want to enter the clinical research industry. No prior CRA experience is required, as Medpace offers its globally recognized PACEยฎ CRA Training Program.

Whether you are a fresher or have up to one year of experience, this Clinical Research Associate Entry Job offers structured training, national travel opportunities, and a long-term career path within one of the world’s leading Contract Research Organizations (CROs).


Medpace CRA Entry Recruitment 2026 โ€“ Overview

ParticularDetails
CompanyMedpace Clinical Research India
PositionClinical Research Associate (CRA) Entry
Experience0โ€“1 Year
LocationNavi Mumbai
Employment TypeFull-Time
IndustryClinical Research / CRO
DepartmentResearch & Development
Travel60โ€“80% across India
TrainingPACEยฎ CRA Training Program
Salaryโ‚น5.5โ€“8.5 LPA (Estimated)

About Medpace

Medpace is a global Contract Research Organization (CRO) providing Phase I to Phase IV clinical development services to pharmaceutical, biotechnology, and medical device companies.

With operations across nearly 40 countries and more than 4,000 employees, Medpace supports drug and medical device development in multiple therapeutic areas including:

  • Oncology
  • Cardiology
  • Metabolic Diseases
  • Endocrinology
  • CNS
  • Anti-Infectives
  • Medical Devices

Clinical Research Associate (CRA) Entry Responsibilities

As a Clinical Research Associate, you will be responsible for:

  • Conducting Site Qualification Visits (SQV)
  • Site Initiation Visits (SIV)
  • Routine Monitoring Visits
  • Close-Out Visits (COV)
  • Reviewing investigator qualifications
  • Verifying source documents and Case Report Forms (CRFs)
  • Ensuring protocol compliance
  • Monitoring patient recruitment and retention
  • Reviewing regulatory documentation
  • Managing investigational product accountability
  • Reviewing adverse events (AE) and serious adverse events (SAE)
  • Preparing monitoring reports
  • Communicating with investigators, coordinators, and site staff
  • Ensuring compliance with ICH-GCP, SOPs, and regulatory requirements

Eligibility Criteria

Candidates should possess:

  • Bachelor’s Degree (Preferred in Health Sciences or Life Sciences)
  • B.Pharm
  • Pharm.D
  • M.Pharm
  • Biotechnology
  • Microbiology
  • Nursing
  • Physiotherapy
  • Biomedical Sciences
  • Clinical Research
  • Pharmacy Technician
  • Research Assistant experience (Preferred)

Freshers are encouraged to apply.


Skills Required

  • Clinical Research knowledge
  • GCP understanding
  • Clinical Trial awareness
  • Communication skills
  • Documentation skills
  • Microsoft Office
  • Presentation skills
  • Attention to detail
  • Regulatory compliance
  • Monitoring skills

PACEยฎ CRA Training Program

One of the biggest advantages of joining Medpace is its internationally recognized PACEยฎ Training Program, which includes:

  • Comprehensive CRA training
  • Practical monitoring exercises
  • Site visit simulations
  • Clinical research department rotations
  • Therapeutic area exposure
  • Regulatory training
  • Hands-on mentoring

No previous CRA experience is required.


Employee Benefits

Medpace offers:

  • Competitive salary
  • Travel bonuses
  • Flexible work environment
  • Paid Time Off (PTO)
  • Career progression pathway
  • Professional development programs
  • Employee wellness initiatives
  • Appreciation events
  • Leadership opportunities

Why Choose Medpace?

Working at Medpace provides exposure to:

  • Global clinical trials
  • Pharmaceutical research
  • Medical device studies
  • Oncology research
  • Regulatory affairs
  • Site monitoring
  • International CRO operations

It is an excellent starting point for professionals aiming to build long-term careers in Clinical Research, Clinical Operations, or Clinical Trial Management.


How to Apply

Application Link

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