Fortrea Hiring for Pharm D Freshers in Drug Safety | PSPM Support Associate | Apply Now
Looking for a Pharm D Freshers Job in the Pharmacovigilance industry? Fortrea is hiring for an exciting PSPM Support Associate role in Bangalore. This Drug Safety Jobs opportunity is ideal for Pharm D Fresher candidates interested in Clinical Safety, adverse event processing, post-marketing surveillance, and global pharmacovigilance operations.
- Position Title: PSPM Support Associate
- Location: Bangalore
- Job Requisition ID: 262083
About the Company
Fortrea is a global contract research organization providing clinical development, patient access, and technology solutions to pharmaceutical, biotechnology, and medical device companies worldwide. The company supports Clinical Safety, Pharmacovigilance, and post-marketing surveillance activities across global healthcare projects.
Job Description
- Assist in Clinical Safety and Pharmacovigilance (PSS) operations at Fortrea
- Handle adverse event cases from clinical trials and post-marketing activities
- Process and submit safety reports to clients and regulatory authorities within timelines
- Support Global Safety Leads in project coordination and safety documentation
- Help with reconciliation activities and safety reporting operations
- Gain exposure to Drug Safety, Pharmacovigilance, and Clinical Safety processes
Key Responsibilities
- Support the setup, maintenance, and closure of global or regional clinical trials and post-marketing projects
- Assist in preparing Safety Management Plans (SMPs), reconciliation plans, and safety-related documents
- Help create study-specific job aids, training materials, instructions, and templates
- Support system setup during study startup and ongoing project activities
- Assist with project management tasks such as access requests and training assignments
- Support reconciliation of safety databases when required
- Help prepare and deliver safety presentations to internal and external stakeholders
- Generate monthly status reports and project-specific reports with accurate data and metrics, ideal for Drug Safety Jobs.
- Assist in TMF (Trial Master File) management activities
- Support the preparation of safety documentation for audits and inspections
- Maintain knowledge of SOPs and other controlled safety documents
- Ensure safety reporting compliance with US and international regulations
- Demonstrate strong professional skills, teamwork, and company values consistently
Qualifications
- PharmD + 1 year of relevant experience, ideal for Pharm D Freshers Job.
- For PharmD, a one-year residency or fellowship can be considered as relevant experience.
Experience
- High degree of accuracy with attention to detail.
- Functions as a team player and offers peer support as needed.
- Good written and verbal communication skills.
- Ability to work independently with moderate supervision.
- Good keyboard skills with knowledge of MS Office and Windows applications would be beneficial.
- Mentoring skills preferred
