Are you passionate about clinical research and ensuring the safety of life-changing drugs? If so, Novotech’s Drug Safety Associate position in Bangalore, India, might just be your dream job. Posted on February 21, 2025, this role is trending in the pharma job market, and for good reason—it’s a chance to make a real impact in pharmacovigilance while growing your career with a global leader. At Pharmabharat.com, we bring you the latest pharma job opportunities from top companies like Novotech, so you don’t have to scour multiple portals. Let’s dive into what this role offers!
What Does a Drug Safety Associate Do?
Imagine being the guardian of drug safety, ensuring patients and clinical trials stay protected. As a Pharmacovigilance Associate at Novotech, your core purpose is to monitor and manage safety data from clinical studies and post-marketing surveillance. This isn’t just a desk job—it’s a dynamic role where you’ll handle everything from processing adverse event reports (ICSRs, SAEs, SUSARs) to submitting them in line with global regulations like ICH-GCP.
Key Responsibilities That Matter
Here’s what you’ll be doing, ranked by importance:
- Project Management: You’ll prepare safety management plans, set up safety databases, and even create slides for project kick-offs. It’s about laying the groundwork for success.
- Case Processing: Draft safety narratives, monitor the safety mailbox, and file critical documents in the Trial Master File (TMF). Precision is key here.
- Regulatory Compliance: Submit reports to agencies on time and track submissions—because deadlines save lives.
- Collaboration: Work with medical monitors, drug safety physicians, and study teams to clarify data and ensure smooth operations.
- Training: Mentor junior staff and share your expertise—because great teams grow together.
Other tasks include unblinding procedures, literature searches for adverse events, and supporting audits. It’s a role that keeps you on your toes!
Who Should Apply?
Novotech is looking for sharp, dedicated candidates with the right qualifications and skills. Here’s what you’ll need:
Education and Experience
- A degree as a registered nurse, pharmacist, or in health/biomedical sciences is a must. Bonus points for postgraduate qualifications or clinical trial certifications!
- 2–4 years of experience in pharmaceuticals or a CRO, with a focus on safety in clinical trials. If you’ve handled case processing or regulatory reporting, you’re already ahead.
Skills That Set You Apart
- Strong knowledge of pharmacovigilance and clinical trial regulations—think ICH-GCP and SOPs.
- Familiarity with medical coding (e.g., MedDRA) and safety databases.
- Excellent English communication skills and the ability to summarize complex medical data.
- Time management and multitasking chops—because no two days are the same.
Why Join Novotech?
Novotech isn’t just any employer. With 34 offices worldwide and over 3,700 clinical projects under its belt, this CRO is a powerhouse in biotech and clinical research. Based in Bangalore’s Helios Business Park, this role offers a vibrant workplace with flexible hours, paid parental leave, and wellness programs. Novotech’s commitment to inclusivity—supporting LGBTIQ+ individuals, people with disabilities, and caregivers—makes it a standout choice. Plus, their ISO 27001 and ISO 9001 certifications ensure top-notch security and quality standards.
A Growing Field
Pharmacovigilance is booming in India, with the market expected to grow at a CAGR of 11.5% through 2030 (source: Mordor Intelligence). Roles like this are in high demand as global trials expand, making now the perfect time to jump in.
Apply Before 28th Feb 2025
