Job Summary
- Position: Pharmacovigilance Executive (ICSR Processing)
- Location: Thane, Maharashtra (Work From Office)
- Experience Level: Freshers
- Employment Type: Full-time
- Qualifications: B.Pharm or M.Pharm
- Vacancies: 1
Company Overview
We are currently seeking a motivated and detail-oriented Pharmacovigilance Executive to join our team in Thane. This position is ideal for entry-level professionals who are looking to build a strong foundation in drug safety and regulatory compliance within the pharmaceutical industry.
Role Responsibilities
As a Pharmacovigilance Executive specializing in Individual Case Safety Report (ICSR) processing, your primary responsibilities will include:
- Performing end-to-end adverse event case processing (ICSR).
- Ensuring the accurate and timely entry of safety data into the designated safety databases.
- Conducting thorough reviews and analyses of safety data to ensure high-quality reporting.
- Supporting various pharmacovigilance activities while strictly adhering to internal protocols and global regulatory guidelines.
Skills and Qualifications
We are looking for candidates who possess a solid academic background and a keen interest in drug safety. The ideal candidate should meet the following requirements:
- Educational Background: A degree in B.Pharm or M.Pharm.
- Technical Skills: A basic understanding of safety databases is highly desirable.
- Functional Knowledge: Prior knowledge or academic coursework in pharmacovigilance processes is preferred.
- Analytical Ability: Strong analytical skills with high attention to detail.
- Communication: Excellent written and verbal communication skills, including the ability to maintain precise documentation.
- Academic Record: Candidates with strong and relevant academic credentials will be given preference.
Internship Opportunity: Clinical Research Coordinator (CRC)
In addition to our Pharmacovigilance role, we are also accepting applications for a Clinical Research Coordinator (CRC) Internship based in Navi Mumbai.
Internship Details:
- Role: Clinical Research Coordinator (CRC) Intern
- Location: Navi Mumbai
- Vacancies: 2
- Eligibility: B.Pharm, M.Pharm, B.Sc/M.Sc in Life Sciences, Pharm.D, or graduates/students of Clinical Research programs.
- Note: Immediate joiners are highly preferred. Please be advised that charges are applicable for this internship program.
Program Highlights:
- Hands-on learning experience in the field of clinical research.
- Opportunity to work on research paper publications.
- A formal certificate will be provided upon successful completion of the internship.
Key Learning Areas for Interns:
- Clinical trial documentation, including Case Report Forms (CRF) and eCRF.
- Comprehensive training on Good Clinical Practice (GCP) and regulatory guidelines.
- Practical exposure to site management and monitoring basics.
- Fundamentals of Data Management and Pharmacovigilance.
- Insight into Ethics Committee operations and the clinical trial life cycle.
Application Process
If you are a dedicated professional looking to kickstart your career in the pharmaceutical sector, we invite you to apply. Please submit your updated CV to the contact information provided below.
- Email Address: [email protected]
- Contact Number: +91 9356325933
When applying, please ensure your email includes a clear subject line indicating the position you are interested in. We look forward to reviewing your application and discussing how you can contribute to our team.