Parexel Hiring Drug Safety Associate I
Are you passionate about drug safety and pharmacovigilance? Do you have a background in pharmacy, life sciences, nursing, or a related field? If you’re looking for an opportunity to kickstart your career in the pharmaceutical industry, Parexel is hiring Drug Safety Associate I in Mohali, India. This is a full-time, entry-level role that offers a dynamic work environment, professional growth, and the opportunity to contribute to global healthcare. Parexel Hiring Drug Safety Associate I
About Parexel
Parexel is a leading global biopharmaceutical services company that partners with pharmaceutical, biotech, and medical device organizations to drive innovation in healthcare. With a strong commitment to patient safety, regulatory compliance, and clinical research, Parexel plays a critical role in the development of life-saving drugs and therapies.
At Parexel, employees enjoy a collaborative work culture, opportunities for skill development, and a focus on work-life balance. If you’re eager to make a meaningful impact in drug safety and regulatory affairs, this is the perfect place to grow your career. Parexel Hiring Drug Safety Associate I
Position: Drug Safety Associate I
📍 Location: Mohali, India
📅 Application Deadline: February 14, 2025
🎓 Qualification: M.Pharm, MSc, Pharm.D, Life Sciences, Nursing, or relevant degree
💼 Experience Required: 0 – 1 year (Freshers can apply!)
✅ Job Type: Verified Job | Online Application
Key Responsibilities
As a Drug Safety Associate I, you will play a key role in drug safety management, ensuring compliance with regulatory requirements and maintaining pharmacovigilance standards. Your responsibilities will include:
1. Safety Data Management:
- Review, process, and analyze safety data from clinical trials and post-marketing reports.
- Perform triage of incoming safety reports, checking completeness and validity.
- Enter case reports into safety databases and manage follow-up queries.
- Code data using MedDRA and write case narratives.
2. Compliance & Regulatory Support:
- Assist in developing safety procedures, workflows, and templates for projects.
- Support regulatory submissions, expedited reporting, and case tracking.
- Ensure adherence to Standard Operating Procedures (SOPs) and global regulatory requirements.
- Participate in audits, inspections, and client meetings as needed.
3. Medical & Scientific Support:
- Collaborate with Medical Directors and Safety Physicians on case assessments.
- Conduct literature searches and assist in signal detection activities.
- Maintain and manage safety documentation and project-specific files.
Skills & Qualifications Required
✔ Educational Qualification:
- Master’s degree in Pharmacy, Life Sciences, Nursing, or a related health field.
- Candidates with equivalent qualifications or relevant work experience will also be considered.
✔ Technical & Soft Skills:
- Strong analytical and problem-solving abilities.
- Excellent communication skills (written & verbal).
- Ability to perform database and literature searches.
- Strong organizational and prioritization skills.
- Proficiency in MS Office and pharmacovigilance tools.
- Detail-oriented mindset with a focus on accuracy and compliance.
✔ Work Experience:
- 0 – 1 year of experience (fresh graduates welcome!).
- Prior experience in pharmacovigilance, clinical research, or healthcare is an advantage.
Why Join Parexel?
🌍 Global Impact: Be part of a team dedicated to improving global patient safety.
📈 Career Growth: Gain industry experience and opportunities for professional development.
🤝 Collaborative Environment: Work with world-class experts in a dynamic setting.
🏡 Work-Life Balance: Supportive and flexible work culture.
🔒 Job Security & Benefits: Competitive salary, insurance, and employee wellness programs.
How to Apply?
If you’re ready to launch your career in drug safety and pharmacovigilance, apply now! The deadline for applications is February 14, 2025.
Start your journey with Parexel and contribute to global healthcare advancements! 🚀 Parexel Hiring Drug Safety Associate I
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