Here’s an opportunity for fresh graduates and early-career professionals who want to enter the CRO and clinical research industry.
Medpace is hiring for a Clinical Research Associate (CRA) – Entry position in Navi Mumbai.
What makes this opportunity interesting for beginners is the structured PACE® CRA Training Program, designed to help candidates develop the knowledge and practical skills needed for a career in clinical monitoring.
Job Overview
| Particulars | Details |
|---|---|
| Position | Clinical Research Associate (CRA) – Entry |
| Company | Medpace Clinical Research India |
| Job Type | Full-Time |
| Category / Department | Research |
| Application Mode | Online |
🏢 About Medpace Clinical Research India
Medpace is a global Contract Research Organization (CRO) that works with pharmaceutical, biotechnology, and medical device companies involved in clinical development.
Its services support different stages of clinical research, including areas such as:
✔️ Study management
✔️ Clinical monitoring
✔️ Data management
✔️ Regulatory submissions
✔️ Clinical trial operations
✔️ Other services required to support successful studies
The organization works at an important point in the healthcare development process — helping sponsors move potential medicines and medical technologies through clinical research.
💡 Editor's Note / Preparation Tip
If you're a fresher, don't worry if your resume doesn't contain the title "Clinical Research Associate."
Instead, demonstrate your understanding of clinical research.
For example, highlight:
✅ Academic projects related to clinical research
✅ Clinical trial knowledge
✅ GCP training or certification
✅ Pharmacovigilance exposure
✅ Regulatory knowledge
✅ Research projects
✅ Hospital / clinical experience
✅ Data documentation
✅ Scientific presentations
✅ Internship experience
✅ Relevant pharmaceutical or healthcare coursework
Also make sure your resume clearly shows your degree, relevant skills, certifications, projects, and practical exposure.
🎯 INTERVIEW PREPARATION
Before applying or attending an interview, revise:
🔹 What is a clinical trial?
🔹 Clinical trial phases
🔹 Role of a CRA
🔹 What is ICH-GCP?
🔹 What is informed consent?
🔹 Source documents and CRFs
🔹 Site Initiation Visit
🔹 Monitoring visits
🔹 Site Close-Out Visit
🔹 Protocol deviations
🔹 AE vs SAE
🔹 Investigational Product accountability
🔹 Essential clinical trial documents
🔹 Patient recruitment and retention
🔹 Basic regulatory requirements
📝 Job Description
🚨 HIRING ALERT | CLINICAL RESEARCH ASSOCIATE (CRA) – ENTRY | MEDPACE | NAVI MUMBAI
📌 JOB DETAILS
🔹 Position: Clinical Research Associate (CRA) – Entry
🔹 Company: Medpace Clinical Research India
🔹 Location: Navi Mumbai, Maharashtra
🔹 Job Type: Full-Time
🔹 Experience: 0–1 Year
🔹 Industry: Clinical Research / CRO
🔹 Department: Research & Development
🔹 Travel: Approximately 60–80% across India
🔹 Training: PACE® CRA Training Program
🔹 Application Mode: Online
🎓 WHO CAN APPLY?
This opening may be suitable for candidates from healthcare, pharmaceutical, and life-science backgrounds, including:
💊 B.Pharm
💊 M.Pharm
💊 Pharm.D
🧬 Biotechnology
🧫 Microbiology
👩⚕️ Nursing
🧠 Biomedical Sciences
🏥 Physiotherapy
🔬 Clinical Research
💊 Pharmacy Technician
🔬 Research Assistant backgrounds
Freshers and candidates with limited relevant experience can consider applying if they meet the position requirements.
🧪 WHAT DOES A CRA DO?
A Clinical Research Associate plays an important role in keeping clinical studies on track.
Depending on the study and assigned sites, responsibilities may include:
✔️ Supporting site qualification activities
✔️ Participating in Site Initiation Visits
✔️ Conducting routine monitoring activities
✔️ Supporting study close-out activities
✔️ Reviewing investigator and site qualifications
✔️ Checking source documentation and clinical trial records
✔️ Reviewing Case Report Forms and study data
✔️ Following up on patient recruitment and retention
✔️ Checking regulatory and essential documents
✔️ Supporting investigational product accountability
✔️ Reviewing and escalating safety information such as AE/SAE records
✔️ Preparing monitoring-related reports
✔️ Communicating with investigators and study coordinators
✔️ Helping ensure study activities follow the protocol
✔️ Working according to ICH-GCP, SOPs, and applicable regulation
🌱 PACE® CRA TRAINING PROGRAM
One of the key attractions of this entry-level opportunity is Medpace's PACE® CRA Training Program.
For someone starting out, structured training can help bridge the gap between academic knowledge and practical clinical research work.
Training may cover areas such as:
📚 CRA fundamentals
🧪 Clinical monitoring activities
🏥 Site visit simulations
📋 Clinical trial documentation
📑 Regulatory requirements
🌍 Therapeutic-area exposure
🤝 Practical mentoring
🔬 Clinical research processes
This can be particularly useful for graduates who understand clinical research academically but have not yet worked as a CRA.
🌍 WHY MEDPACE?
Clinical research is not just about documentation and monitoring.
Behind every clinical study are patients, investigators, research teams, and potential treatments that may eventually make a difference in healthcare.
Working in a CRO environment can therefore be both challenging and meaningful.
For someone who enjoys healthcare, science, research, and working with different teams, a CRA career can open doors toward:
📈 Clinical Operations
📊 Clinical Trial Management
🧪 Clinical Research
📋 Regulatory Affairs
🏥 Site Management
🌍 Global Clinical Development
💰 SALARY – ESTIMATED
The job information provided indicates an estimated range of:
₹5.5 LPA – ₹8.5 LPA
⚠️ This should be treated as an editorial / market estimate, not an officially confirmed salary range from Medpace. Actual compensation may depend on the role, experience, location, company policies, and other factors.
🎁 POSSIBLE BENEFITS
The supplied information mentions benefits and employee programs such as:
✔️ Professional development opportunities
✔️ Career progression
✔️ Paid time off
✔️ Wellness initiatives
✔️ Travel-related benefits / bonuses
✔️ Employee engagement activities
✔️ Leadership development opportunities
Benefits and eligibility can vary, so candidates should verify the current terms during recruitment.
📌 IMPORTANT FOR APPLICANTS
Job requirements and recruitment timelines can change.
Before submitting your resume, always verify:
✔️ Current job status
✔️ Eligibility criteria
✔️ Location
✔️ Travel requirements
✔️ Application deadline
✔️ Official application link
🚀 WHO SHOULD CONSIDER THIS OPPORTUNITY?
This could be a good opportunity for a recent graduate who wants to move from academic knowledge into practical clinical research.
If you are from a Pharmacy, Biotechnology, Microbiology, Nursing, Biomedical Sciences, Clinical Research, or related healthcare background and want to build a career in clinical trials, this CRA Entry role is worth exploring.
💡 Required Qualifications & Skills
🚀 Career Guidance & Interview Insights
To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.
This Clinical Research Associate (CRA) – Entry role is a chance to contribute directly to life sciences, patient care, or pharmaceutical advancements. You will work within strict compliance frameworks, ensure rigorous quality standards, and collaborate with technical or medical experts. It is a career path that blends scientific excellence with a deep sense of social purpose.
Healthcare and pharmaceutical professionals grow through specialized scientific experience. Entry-level starts as Lab Technician, Chemist, or Quality Associate, progressing to Senior QA/QC Analyst. Advancement leads to Lab Supervisor, Clinical Project Manager, and senior management roles like Quality Director, VP of Regulatory Affairs, or Chief Scientific Officer.
Expected Technical & Behavioral Questions:
- Q1: How do you ensure compliance with WHO/GMP guidelines during laboratory operations?
Answer Tip: Mention strict adherence to Standard Operating Procedures (SOPs), detailed batch records, regular equipment calibration, and sanitization cycles. - Q2: What steps do you take when a quality deviation is detected in a product batch?
Answer Tip: Outline immediate isolation of the batch, raising a deviation report, root cause analysis (RCA), and initiating CAPA (Corrective and Preventive Action). - Q3: How do you manage safety protocols while handling toxic chemicals?
Answer Tip: Discuss using Material Safety Data Sheets (MSDS), wearing appropriate Personal Protective Equipment (PPE), proper ventilation, and chemical spill kits.
To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:
- Keywords to include: Quality Control (QC), GMP Compliance, FDA Regulations, SOP Documentation, HPLC/GC analysis, Batch Validation, Clinical Trials, Pharmacovigilance.
- Format: List laboratory skills and instruments handled (e.g. HPLC, spectrophotometer) in a dedicated technical matrix.
- Quantify Results: E.g., 'Validated 15 batch formulations under GMP guidelines with zero quality defects.'
Estimated compensation for this role type in India is ₹2,40,000 - ₹3,80,000 per annum (Fresher analyst). The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.
Key credentials: GMP Certified Professional (ASQ), Certified Clinical Research Coordinator (CCRC), or specialized laboratory training certificates in high-performance liquid chromatography (HPLC) and safety standards.
Frequently Asked Questions
1. Is this position suitable for freshers?
Yes. The role is specifically positioned as an entry-level CRA opportunity, and candidates with limited experience may be considered.
2. What qualifications are relevant?
Candidates from Pharmacy, Life Sciences, Biotechnology, Microbiology, Nursing, Physiotherapy, Biomedical Sciences, Clinical Research, and related healthcare backgrounds may be relevant.
3. Do I need previous CRA experience?
Previous CRA experience is not necessarily required for this entry-level opportunity. The training program is designed to support candidates entering the CRA profession.
4. Where is the position located?
The position is based in Navi Mumbai, Maharashtra.
5. Is this a work-from-home position?
The role involves clinical monitoring activities and substantial travel, so candidates should be prepared for an on-site and travel-oriented work environment.
6. How much travel is involved?
The supplied job information indicates approximately 60–80% travel across India.
7. What is the PACE® CRA Training Program?
It is a structured training pathway intended to prepare entry-level candidates for responsibilities associated with clinical research and CRA work.
8. What is ICH-GCP?
ICH-GCP refers to international guidelines for conducting clinical trials ethically and with appropriate standards for participant safety, data quality, and study conduct.
9. What career options can follow a CRA role?
Experience as a CRA can potentially lead toward Senior CRA, Clinical Trial Manager, Clinical Operations, Project Management, and other clinical development roles.
10. What salary can I expect?
The supplied listing mentions an estimated range of ₹5.5–8.5 LPA. Candidates should verify the actual compensation directly with the employer.
Share This Job
🛡️ Safety Disclaimer: JobPortalConnect curates official listings for informational purposes. Genuine recruiters will never ask you for processing fees, training payments, or security deposits. If you spot suspicious activity, copyright issues, or wish to request the removal of this listing, please report it to us immediately at contact.jobportalconnect@gmail.com.