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ProPharma
ProPharma is inviting applications for the position of Pharmacovigilance Scientist in Hyderabad, Telangana. Candidates with experience in pharmacovigilance, aggregate safety reporting, signal detection, and medical writing are encouraged to apply for this exciting opportunity.
About ProPharma
For more than 20 years, ProPharma has been helping biotech, pharmaceutical, and medical device companies advance scientific innovations and bring life-changing therapies to patients worldwide. The company provides comprehensive consulting solutions across regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology.
Job Details
| Particulars | Details |
|---|---|
| Position | Pharmacovigilance Scientist |
| Location | Hyderabad, Telangana, India |
| Job Type | Remote (Hyderabad-based candidates preferred) |
| Experience | Minimum 2+ Years |
| Qualification | Bachelor’s or Master’s Degree |
| Department | Pharmacovigilance / Drug Safety |
Key Responsibilities
The selected candidate will be responsible for:
- Authoring aggregate safety reports including:
- PSURs / PBRERs
- PADERs / Annual Reports / ACO
- DSURs
- Preparing and maintaining Risk Management Plans (RMPs)
- Authoring and contributing to Signal Management Reports
- Conducting literature searches, screening, and validity assessments
- Performing duplicate checks and literature reviews using appropriate tools
- Extracting and validating safety data such as RSI, sales data, prior reports, and signals
- Generating and reviewing line listings from safety databases
- Reconciling and maintaining pharmacovigilance process trackers
- Supporting urgent and ad-hoc pharmacovigilance activities
- Ensuring compliance with global regulatory requirements and reporting timelines
- Participating in audits and inspections as a Subject Matter Expert (SME)
- Contributing to SOPs, Work Instructions (WIs), deviations, and CAPA activities
Required Skills & Competencies
Candidates should possess:
- Strong analytical and problem-solving skills
- Excellent attention to detail and commitment to quality
- Effective organizational and time-management abilities
- Strong written and verbal communication skills
- Medical writing expertise
- Ability to summarize and interpret complex scientific data
- Understanding of global pharmacovigilance regulations including ICH-GCP, FDA, and EMA guidelines
- Proficiency in Microsoft Word, Excel, PowerPoint, and web-based applications
- Ability to work effectively in a global and cross-functional environment
Educational Qualification
Applicants should have a Bachelor’s or Master’s degree in:
- Pharmacy
- Nursing
- Life Sciences
- Healthcare or related scientific disciplines
Equivalent industry experience may also be considered.
Experience Required
Candidates must have:
- Minimum 2 years of Pharmacovigilance experience
- Experience in one or more of the following areas:
- Aggregate safety report writing
- Literature search and screening
- Signal detection and management
- Pharmacovigilance medical writing
Preferred Experience
- Authoring and reviewing aggregate safety reports
- Exposure to quality metrics and client interactions
- Experience supporting regulatory compliance activities
Why Join ProPharma?
- Opportunity to work with a globally recognized life sciences consulting organization
- Exposure to international pharmacovigilance and regulatory projects
- Collaborative and professional work environment
- Career growth opportunities in drug safety and risk management
- Flexible remote working model with periodic office collaboration
How to Apply
Interested and eligible candidates can apply through the official ProPharma careers portal. Candidates with relevant pharmacovigilance experience and strong medical writing skills are encouraged to submit their applications at the earliest.
Apply Soon and take the next step in your Pharmacovigilance career with ProPharma!
APPLY HERE
To apply for this job please visit propharmagroup.wd1.myworkdayjobs.com.
