Job Title
PSPM Support Associate
Company
Fortrea
Location
Bangalore, India
Employment Type
Full-time / Pharmacovigilance Support
Role Overview
The PSPM Support Associate supports clinical safety and post-marketing safety (PSS) operations, particularly in the management of adverse event (AE) processing and safety reporting activities. The role assists in ensuring compliant, timely, and accurate submission of safety data to clients and regulatory authorities across clinical trial and post-marketing environments.
This position operates under the guidance of a Global Safety Lead and contributes to safety system setup, maintenance, reporting, and documentation activities in alignment with regulatory requirements and company SOPs.
Key Responsibilities
1. Safety Operations Support
Assist in setup, maintenance, and closeout of global/regional safety projects
Support clinical trial and post-marketing safety activities
Assist in adverse event (AE) processing and reporting
2. Safety Planning & Documentation
Support preparation of:
Safety Management Plans (SMPs)
Reconciliation Plans
Safety-specific study documents
Assist in creation of:
Job aids
Training materials
Process templates
3. Systems & Study Setup Support
Assist in study start-up system configuration
Support ongoing maintenance of safety systems
Help manage access requests and training assignments
4. Safety Data Management
Support reconciliation of safety databases
Assist in tracking and resolving data discrepancies
Contribute to data quality checks and safety reporting accuracy
5. Reporting & Metrics
Support preparation of:
Monthly safety reports
Project-specific status updates
Metrics and performance data
Ensure accuracy and completeness of safety-related reporting
6. Compliance & Documentation
Ensure compliance with:
SOPs
Global safety reporting regulations
US and international pharmacovigilance requirements
Support audit and inspection readiness activities
Assist in Trial Master File (TMF) management
7. Communication & Coordination
Support internal and external stakeholder communications
Assist in preparing safety presentations
Collaborate with Global Safety Leads and project teams
Required Qualifications
Education
One of the following:
Non-degree + 1 year safety experience OR 3 years relevant experience
Associate degree + 1 year experience OR 2 years relevant experience
Bachelor’s degree (BS/BA) + 1 year relevant experience
Master’s degree + 1 year relevant experience
PharmD + 1 year relevant experience
Preferred disciplines:
Biological Sciences
Pharmacy
Nursing
Medical Sciences
Life Sciences
Required Skills & Competencies
Technical & Functional Skills
Understanding of pharmacovigilance and safety operations
Knowledge of AE reporting processes
Familiarity with SOPs and regulatory requirements
Basic MS Office (Excel, Word) skills
Core Competencies
High attention to detail and accuracy
Ability to work independently with moderate supervision
Strong teamwork and collaboration skills
Good organizational ability
Communication Skills
Clear written and verbal communication
Ability to support training and documentation activities
Ability to interact within global teams
Preferred Attributes
Mentoring ability (preferred)
Prior exposure to pharmacovigilance systems or safety operations
Experience in clinical trial or post-marketing safety environments
Work Environment
Office-based or remote setup
Global clinical safety operations environment
Highly regulated pharmacovigilance setting
Collaborative team structure under Global Safety leadership
Company Overview
Fortrea is a global Contract Research Organization (CRO) providing clinical development and pharmacovigilance services across clinical trial and post-marketing phases. The company focuses on ensuring patient safety, regulatory compliance, and high-quality clinical operations across global studies.
Role Summary
The PSPM Support Associate role at Fortrea supports pharmacovigilance and clinical safety operations by assisting with adverse event processing, safety reporting, system setup, and compliance documentation. The position is entry-to-mid level and requires strong attention to detail, regulatory awareness, and the ability to support global safety teams in a structured, compliance-driven environment.
Uttar Pradesh :
Agra | Gajraula | Gautam buddha Nagar | Ghaziabad | Gorakhpur | Greater Noida | Jhansi | kanpur | Lucknow | Mathura | Noida | Park City | Prayagraj | Satyamev | Varanasi |Gujarat :
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Delhi | India | New Delhi | PAN-India |Assam :
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Hajipur | Patna |Kerala :
Kannur | Kochi | Malappuram | Thiruvananthapuram | Trivandrum |Pondicherry (Puducherry) :
Pondicherry (Puducherry) |Jharkhand :
Ranchi |Sikkim :
Rangpo |India :
Remote, India | Siliguri |Illinois :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Duluth | Eden Prairie | Fridley | Hibbing | Maple Grove | Minneapolis and St. Paul, Minnesota. | Minnetonka | St.Paul |Kentucky :
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Frank Scottile Blvd |Missouri :
Fulton | Milan | St. Louis |United States :
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Mexico |northeastern :
New Hampshire |Oklahoma :
Oklahoma City |Puerto Rico :
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Tuscaloosa |D.C :
Washington |Delaware :
Wilmington |North Rhine Westphalia :
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Budapest |BULGARIA :
Bulgaria | Vedant |Denmark :
Copenhagen | Denmark |Europe :
Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
Finland |Istanbul :
Istanbul | Turkey |Norway :
Norway | NOrway |Romania :
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Wavre |Tipperary :
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Brinny | Ringaskiddy |Carlow :
Carlow |Republic of Ireland :
Cork | Dublin | Limerick | Waterford |Ulster :
Donegal |Meath :
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Galway |County Dublin :
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China | Quarry Bay |Liaoning :
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Netherlands |Remote Australia :
Arkansas | Remote Australia |New South Wales :
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Queensland |Melbourne :
South Yarra |United Kingdom :
England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Canada |Quebec :
Montreal |Brussels :
Brussels |Antwerp :
Heist op den Berg |Flemish Brabant :
Zaventem |South America :
Argentina | Peru |Brazil :
Sao paulo | Brazil |Attica :
Koropi | Athens |Greece :
Greece |North Island :
Auckland |New Zealand :
New Zealand |Austria :
Austria |Vienna :
Vienna |Catalonia :
Barcelona |Madrid :
Madrid |Cebu Province :
Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
Estonia | Tartu |Harju County (Maakond) :
Tallinn |Hà Nội :
Hanoi | Hà Nội |Ho Chi Minh :
Ho Chi Minh City |Italy :
Italy |Lombardy :
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Jakarta |East Java :
Surabaya |Japan :
Saitama | Japan |Tokyo :
Otemachi |North Ostrobothnia :
Oulu |Southwest Finland (Varsinais-Suomi) :
Turku |Remote Korea :
Remote Korea |Republic of Korea :
Seoul |Kazakhstan :
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Bangkok |Israel :
Kfar Saba | Netanya | Tel Aviv | Be'Er Sheva | Yavne |Remote :
Slovakia | Thailand | Remote - South America (Latin Americal) | Leinster | Hammond | Bishop | Victoria | Remote, USA | Xzagreb | Belgium | Bountiful | Lousiana | Ireland | Castlebar | Green Way | Blue Bell | Medan | Remote - Europe | Springville | McFarland | Zaragoza | Remote | Switzerland | Lenexa | Faridabad | Remote - Middle East | Nairobi | Minnesota | Tulsa | Regulatory Labeling Manager (NA and LATAM Only) | Hungary | Remote - Africa | Manipal | Riga | Texas | Melbourne | French |Republic of Colombia :
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Kyiv |Lima Region :
Lima |France :
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Midrand | South Africa |Nišava District :
Niš |Bohemia :
Prague |Chile :
Santiago |Bosnia and Herzegovina :
Sarajevo |Singapore :
Singapore |Sofia City :
Sofia |Sweden :
Sweden |Taipei :
Taipei |Mazovia :
Warsaw |