PHARMAFull-time
Clinical Research Associate (CRA) Entry
MUMBAI (IN)ONSITEPOSTED: 7/5/2026
PHARMAFull-time
HIRING ORGANIZATIONMEDPACE, INC.Clinical Research / Pharmaceutical Services
ROLE DEFINITION & 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
REQUIRED VERIFIED SKILLS
Clinical Research knowledge
GCP understanding
Clinical Trial awareness
Communication skills
Documentation skills
Attention to detail
Regulatory compliance
Monitoring skills
COMPENSATION & REWARDS
₹5.5L - 8.5L per annum
The estimated salary package ranges from ₹5.5 to 8.5 LPA, which is highly competitive for entry-level positions in the clinical research industry, complemented by travel bonuses and employee wellness initiatives.
ORGANIZATION CONTEXT & CULTURE
Medpace, Inc. is a global full-service clinical research organization (CRO) that provides scientifically-driven clinical development services to the pharmaceutical, biotechnology, and medical device industries. They specialize in conducting Phase I-IV clinical trials across various therapeutic areas, leveraging deep therapeutic expertise to accelerate the development and approval of new drugs and devices. Medpace aims to bring new and effective medical products to patients faster.
TEAM SIZE: 5,001-10,000 employees
INDUSTRY: Clinical Research / Pharmaceutical Services
EXPECTED CAREER ROADMAP
Medpace offers its globally recognized PACE® CRA Training Program, providing a structured career progression pathway, professional development programs, and leadership opportunities within one of the world's leading global Contract Research Organizations (CROs).
APPLICATION ADVISORY
Highlight your clinical trial awareness, understanding of GCP guidelines, and strong communication skills during the interview. Emphasize any health or life sciences academic projects or relevant pharmacy technician/research assistant experience.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.