"Syneos Health Hiring Safety & PV Coordinator in Hyderabad | Pharmacovigilance Jobs"

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"Syneos Health Hiring Safety & PV Coordinator in Hyderabad | Pharmacovigilance Jobs" (Syneos Health Hiring Safety & PV Coordinator in Hyderabad) Introduction Candidates looking to build a strong and long-term career in Pharmacovigilance (PV) and Drug Safety have an excellent opportunity at Syneos Health , a globally recognized biopharmaceutical solutions organization. Syneos Health is currently hiring for the position of Safety & PV Coordinator at its Hyderabad office . This is a full-time, office-based role , ideal for professionals who have experience or exposure in pharmacovigilance submissions, safety reporting, regulatory compliance, and clinical research processes . Working with a global organization like Syneos Health provides exposure to international safety regulations, cross-functional teams, and structured career growth . About The Company – Syneos Health Syneos Health® is a fully integrated biopharmaceutical solutions organization that supports pha...

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"Clinical Research Associate (CRA) Jobs at HRAPL – Apply Now for Exciting Career Opportunities in Nagpur"

"Clinical Research Associate (CRA) Jobs in Nagpur | HRAPL Hiring Life Science & Pharmacy Graduates."

(Clinical Research Associate (CRA) Jobs)

Location: Nagpur, Maharashtra
Company: HRAPL (Healthcare Research & Analytics Pvt. Ltd.)
Employment Type: Full-Time | On-Site

Build Your Career in Clinical Research with HRAPL:-Are you a passionate Clinical Research Associate (CRA) seeking the next big step in your career?

HRAPL, one of India’s most trusted Clinical Research Organizations (CROs), is inviting applications from skilled and motivated professionals for CRA positions in Nagpur, Maharashtra.
If you hold a degree in Life Sciences, Pharmacy, or Biotechnology and have 2–4 years of experience in clinical research, this opportunity will allow you to contribute to impactful healthcare advancements across India.

About HRAPL – Advancing Clinical Research in India:-

HRAPL is a pioneer in India’s clinical research landscape, dedicated to delivering reliable, ethical, and data-driven research solutions for global and domestic pharmaceutical partners.
With a strong focus on Good Clinical Practice (GCP) and regulatory compliance, HRAPL continues to empower the healthcare industry through innovation, transparency, and talent development.
Their mission is to strengthen India’s position as a hub for high-quality clinical trials that transform patient care and drug development outcomes.

Job Role: Clinical Research Associate (CRA):-

As a CRA at HRAPL, you will play a key role in managing and monitoring clinical trial activities at investigator sites.
You’ll ensure that studies are conducted according to protocols, ICH-GCP guidelines, and ethical standards.

Key Responsibilities:

Conduct site selection, initiation, routine monitoring, and close-out visits.
Ensure compliance with study protocols, SOPs, and ethical regulations.
Perform source data verification to validate CRF accuracy.
Maintain and update Essential Documents and Investigator Site Files (ISF).
Oversee investigational product accountability and site documentation.
Support regulatory audits, inspections, and sponsor communications.
Foster effective collaboration with investigators, study teams, and sponsors.

Required Qualifications & Skills:-

Education: B.Pharm / M.Pharm / B.Sc / M.Sc in Life Sciences, Pharmacy, or related fields.
Experience: 2–4 years as a Clinical Research Associate (CRA).
Knowledge: Strong understanding of ICH-GCP, clinical operations, and regulatory frameworks.
Technical Skills: Excellent documentation, reporting, and data accuracy.
Soft Skills: Communication, critical thinking, and time management abilities.
Location: Nagpur (Candidates across India willing to relocate can apply).

Why Join HRAPL?

Work with a leading Indian CRO engaged in global research projects.
Get hands-on exposure to cutting-edge clinical studies.
Enjoy a collaborative and ethical work culture focused on learning.
Opportunities for career advancement in clinical operations and management.
Make a real difference in improving patient outcomes and drug safety.

How to Apply for HRAPL CRA Jobs:-

If you meet the eligibility criteria and are ready to grow in clinical research, follow these steps:

Update your latest resume (highlighting CRA experience).
Write a short cover email mentioning your interest in the CRA role.
Send your application to: 📩 Contact@hrapl.in.
Mention in the subject line: Application for CRA Position – Nagpur
Deadline: Applications open until positions are filled. Apply early to secure your chance!

Quick Overview:-

Position Clinical Research Associate (CRA)
Company HRAPL
Location Nagpur, Maharashtra
Experience 2–4 Years
Education Life Sciences / Pharmacy / Biotechnology
Job Type Full-Time
Email Contact@hrapl.in

FAQs – Clinical Research Associate Jobs at HRAPL:-

Q1: What experience is required for the CRA role at HRAPL?
A minimum of 2 years of hands-on clinical trial monitoring experience is required.

Q2: Is relocation assistance available for outstation candidates?
Yes, HRAPL welcomes applicants from across India who are open to relocating to Nagpur.

Q3: What type of studies will the CRA work on?
You will contribute to multicenter clinical trials across therapeutic areas such as oncology, cardiology, and general medicine.

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