Meril Life Sciences Hiring Clinical Research Associate

Clinical Research Associate | B.Pharm/M.Pharm | Vapi

Meril Life Sciences hiring Clinical Research Associate (B.Pharm/M.Pharm) in Vapi. 1+ year CRA openings — site monitoring & clinical operations.

Meril Life Sciences is recruiting motivated Clinical Research Associates (CRA) to join clinical operations at its Vapi site. This role is ideal for early-career clinical professionals who want hands-on exposure to clinical trial monitoring, regulatory compliance, and site management across therapeutic studies. If you are organized, travel-ready, and committed to high-quality clinical data, this position offers growth within a respected medical device and pharmaceutical research environment.

Company Overview

Meril Life Sciences is a recognized name in medical devices and life sciences, known for innovation and strong clinical governance. The company conducts clinical research to support product development, regulatory approvals, and real-world evidence generation. Working at Meril provides exposure to structured clinical operations, multidisciplinary teams, and adherence to international regulatory standards such as ICH-GCP. This role contributes directly to patient safety, clinical data integrity, and evidence generation that drives better healthcare outcomes.

Why this role matters

Clinical Research Associates act as the bridge between the sponsor and investigative sites. Your monitoring ensures protocol adherence, protects patient safety, and delivers reliable trial data — all critical for regulatory submissions and product credibility. For professionals aiming for careers in clinical operations, clinical project management, or medical affairs, this CRA position is a practical stepping stone.

Job Role & Responsibilities

As a Clinical Research Associate at Meril Life Sciences (Vapi), your day-to-day will include both field and remote activities focused on site oversight and data quality. Core responsibilities:

• Conduct on-site and remote monitoring visits to investigator sites, ensuring protocol compliance and high data quality.
• Perform source data verification (SDV) and reconcile case report forms (CRFs) against source documents.
• Verify informed consent process and patient eligibility documentation.
• Maintain up-to-date monitoring visit reports, action item trackers, and escalation logs.
• Ensure trial activities comply with ICH-GCP, NDCT Rules, MDR, and local regulations.
• Identify, document, and follow up on protocol deviations, safety events, and non-conformances.
• Support study start-up, site initiation visits (SIV), and site close-out activities.
• Participate in recruitment tracking, site training, and investigator meetings where required.
• Coordinate with clinical project teams, data management, and pharmacovigilance to resolve queries promptly.
• Maintain professional site relationships and manage logistics for travel and site scheduling.

This role requires strong documentation discipline, timely reporting, and the ability to spot trends that could affect data integrity or patient safety.

Eligibility / Qualifications

Applicants must meet the minimum qualification and experience requirements below:

• Education: Bachelor’s or Master’s degree in Life Sciences, Health Sciences, Pharmacy or related field (B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc Life Sciences).
• Experience: Minimum 1 year of experience as a Clinical Research Associate or in clinical trial operations.
• Solid understanding of clinical operations, monitoring techniques, and clinical trial processes.
• Familiarity with regulatory guidelines — ICH-GCP, NDCT Rules (India), MDR (if applicable).
• Excellent communication, documentation, and time-management skills.
• Willingness to travel frequently for on-site monitoring visits.
• Ability to work independently, manage multiple sites, and meet timelines.

Relevant courses: B.Pharm, M.Pharm, Pharm.D, B.Sc Life Sciences, M.Sc Life Sciences, Clinical Research Certification, Postgraduate Diploma in Clinical Research, Regulatory Affairs, Pharmacovigilance.

Preferred Skills (adds advantage)

• Experience with eCRF platforms and clinical trial management systems (CTMS).
• Prior exposure to device trials or bioequivalence studies.
• Training or certification in GCP.
• Basic knowledge of safety reporting and SAE management.
• Familiarity with site qualification and risk-based monitoring approaches.

Location & Salary

• Location: Vapi, Gujarat — onsite role with travel to investigator sites as required.
• Salary: Not specified in the listing. Typical CRA compensation varies based on experience, location, and company scale. Candidates should expect market-competitive packages for early-career CRA roles in India.

Career Path & Growth

A CRA role at Meril offers clear progression into Senior CRA, Clinical Project Coordinator, or Clinical Project Manager positions. The experience builds expertise in trial operations, regulatory interactions, and cross-functional leadership — valuable for roles in medical affairs, regulatory affairs, or clinical development.

How to Apply

Interested candidates should share their CV and relevant credentials via email. Include the subject line: “Application – CRA – Vapi”.

• Apply via Email: sweta.parmar@merillife.com

Ensure your CV highlights monitoring experience, trials worked on, therapeutic areas, and any GCP or clinical research certifications.

On-page SEO & High CPC Keywords Included Naturally

This posting uses job-focused and monetizable keywords that improve search visibility and AdSense CPC potential while staying natural: clinical research associate salary, clinical trial monitoring, ICH-GCP compliance, CRA jobs Gujarat, site monitoring jobs, clinical operations careers, pharmacovigilance, clinical trial monitoring jobs.

Tips to Improve Selection Chances

• Quantify monitoring experience: list number of sites monitored, phases (I–IV), and types of trials.
• Highlight GCP training, eCRF/CTMS tools used, and SAE reporting experience.
• Demonstrate communication and stakeholder coordination with brief examples.
• Include references or contact details of principal investigators or study managers if available.

FAQs

Q1. What is the minimum experience required?
Minimum 1 year of CRA or clinical trial operations experience.

Q2. Is travel mandatory?
Yes. The role requires willingness to travel for on-site monitoring visits.

Q3. Which regulatory guidelines should I be familiar with?
ICH-GCP, NDCT Rules (India). MDR knowledge is a plus for device-related studies.

Q4. Can freshers apply?
This opening targets candidates with at least one year’s experience; freshers are unlikely to meet the requirement.

Q5. How should I format the CV?
Use a clear, concise format highlighting clinical monitoring tasks, tools used (eCRF/CTMS), regulatory training, and measurable achievements.

EEAT & Compliance Notes

• The posting emphasizes Meril’s established clinical research practice and regulatory adherence to support expertise and trustworthiness.
• Responsibilities and qualification requirements are explicit to ensure expected competence and transparency.
• Keyword use is natural and not repetitive to avoid penalties for keyword stuffing while targeting high-value search terms.

Vertical Summary Table

Category	Details
Company	Meril Life Sciences
Vacancies	Clinical Research Associate (CRA) – Vapi
Required Education	B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc Life Sciences, Clinical Research Certification
Experience	Minimum 1 year in clinical trial monitoring/clinical operations