Abbott Pharmacovigilance Hiring PV Specialist

Abbott Pharmacovigilance Jobs – PV Specialist – Mumbai

Apply for PV Specialist at Abbott, Mumbai. Experienced professionals in Pharmacovigilance, Medical Affairs. Secure your role now!

Abbott, a global leader in healthcare and medical innovations, is seeking a highly skilled PV Specialist for its Mumbai office. This is an exciting opportunity for professionals with expertise in pharmacovigilance and medical affairs to contribute to the safety and efficacy of Abbott’s products in India.

Company Overview

Abbott is a multinational healthcare company with a strong presence in diagnostics, medical devices, nutrition, and branded generic pharmaceuticals. With decades of experience, Abbott emphasizes research-driven innovations, patient safety, and regulatory compliance. The company has earned a reputation for excellence, ensuring that its workforce operates within a culture of integrity, collaboration, and continuous professional development.

Job Role & Responsibilities

The PV Specialist plays a critical role in Abbott’s Medical and Clinical Affairs team, focusing on pharmacovigilance and clinical safety monitoring. Key responsibilities include:

• Overseeing the planning, execution, and monitoring of clinical trials and research activities.
• Implementing clinical protocols and facilitating the completion of final study reports.
• Recruiting clinical investigators and negotiating study design and associated costs.
• Directing human clinical trials, including phases III and IV, for Abbott’s products under development.
• Participating in adverse event reporting and monitoring safety responsibilities.
• Coordinating and providing reports for submissions to regulatory agencies.
• Ensuring adherence to study protocols and determining study completion.
• Coordinating investigator initiations and overseeing group studies.
• Acting as a consultant or liaison with other corporations under licensing agreements.
• Maintaining accurate documentation and ensuring compliance with local and global regulatory requirements.

Eligibility / Qualifications

• Educational Qualification: Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related field.
• Experience: Proven experience in pharmacovigilance, medical affairs, or clinical research.
• Skills: Knowledge of adverse event reporting, clinical trial regulations, regulatory submissions, and safety monitoring.
• Competencies: Strong analytical skills, attention to detail, communication skills, and ability to work independently.

Relevant Courses: B.Pharm, M.Pharm, M.Sc in Life Sciences, Biotechnology, Clinical Research, Pharmacology, Pharmacy, Medical Affairs.

Location & Salary

• Location: Mumbai, India.
• Salary: Not disclosed, aligned with industry standards.

Application Process

Interested candidates can apply directly through Abbott’s official careers page: Apply Here

Apply today to advance your career in Pharmacovigilance with Abbott!

FAQs

Q1: What is the primary role of the PV Specialist?
A1: The PV Specialist oversees pharmacovigilance activities, clinical trials, adverse event reporting, and ensures regulatory compliance for Abbott products.

Q2: What are the required qualifications?
A2: Candidates should have a degree in Pharmacy, Life Sciences, or a related field, preferably with experience in pharmacovigilance or clinical research.

Q3: Where is this position located?
A3: Mumbai, India.

Q4: How can I apply for this role?
A4: Apply through Abbott’s careers page: https://www.jobs.abbott/us/en/job/ABLAUS31131765ENUSEXTERNAL/PV-Specialist

Q5: What experience is preferred?
A5: Professionals with experience in pharmacovigilance, medical affairs, clinical trial monitoring, and regulatory submissions are preferred.

Q6: Is this a full-time role?
A6: Yes, this is a full-time, permanent position.

Summary Table

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