Job Description

Skill required: Pharmacovigilance – Pharmacovigilance & Drug Safety Surveillance

Designation: Drug Safety Associate

Job Location: Bengaluru

Qualifications: Bachelor of Pharmacy/Master of Pharmacy/Bachelor in Physiotherapy/Master Of Physiotherapy

Years of Experience: 0-1 years

iPhone 15 launching in 9 days: Expected price, design, upgrades, specs, and more

 Follow us on Instagram for Private and Govt Job Updates – Click Here to Follow

What would you do?

You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings – Clinical, Pharmacovigilance & Regulatory, helping the world’s leading biopharma companies bring their vision to life – enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience. You will be part of a dynamic Pharmacovigilance team with array of capabilities ranging from detection, assessment, understanding and prevention of adverse effects or any other medicine/vaccine related problem following Good Pharmacovigilance Practice (GVP) per client SOPs and applicable global regulatory requirements (Individual Case Safety Reports) to working on various aspects of Aggregate reports such as planning, authoring, reviewing  and publishing of PBRER, PSUR, DSUR, PADER, Addendum to clinical overview (AdCO), Risk Management Plan (RMP), Signal detection and validation reports (SDVR), Cosmetovigilance Safety Reports (CoSR). The Pharmacovigilance team is also responsible for authoring and reviewing clinical documents such Protocols and amendment, Investigator Brochure, Clinical Study Reports (CSR), Synoptic/Abbreviated CSR, Safety Narratives, Clinical Overview/abbreviated Clinical Overview. In this role, you will be expected to create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements.

 Follow us on Instagram for Private and Govt Job Updates – Click Here to Follow

Join our Whatsapp Group for latest government job updates – Click Here to Join our WhatsApp Group

 From below link, you can join our Telegram Channel – Click Here to Join our Telegram Group

What are we looking for?

• Ability to perform under pressure
• Ability to work well in a team
• Adaptable and flexible
• Agility for quick learning
• Written and verbal communication

Roles and Responsibilities

• In this role you are required to solve routine problems, largely through precedent and referral to general guidelines
• Your expected interactions are within your own team and direct supervisor
• You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments
• The decisions that you make would impact your own work
• You will be an individual contributor as a part of a team, with a predetermined, focused scope of work
• Please note that this role may require you to work in rotational shifts

 Follow us on Instagram for Private and Govt Job Updates – Click Here to Follow

Join our Whatsapp Group for latest government job updates – Click Here to Join our WhatsApp Group

 From below link, you can join our Telegram Channel – Click Here to Join our Telegram Group

Click Here To Apply