POSITION: Clinical Safety Specialist
Type: Contract (hourly)
Duration: 6 months with possibility of extension
REPORTS TO: Director, Clinical Safety
The Clinical Safety Specialist supports the collection, processing, and oversight of clinical trial safety data. The role collaborates closely with Senior Clinical Safety Specialists and cross-functional partners, including Clinical Operations, Data Management, Quality Assurance, and Safety Working Groups, to ensure regulatory compliance and alignment with departmental objectives.
GENERAL DUTIES AND ESSENTIAL JOB FUNCTIONS:
- Receive, review, triage, and process adverse event and other safety information from clinical trials in accordance with applicable regulatory requirements, QLHC SOPs, Work Instructions, and project-specific plans.
- Perform initial assessments of seriousness, expectedness, causality, and regulatory reportability, escalating safety issues per defined governance and escalation pathways.
- Enter, maintain, and quality-check adverse event data in the QLHC safety database, including accurate MedDRA coding and clear, concise, and compliant case narratives.
- Proactively identify missing, inconsistent, or unclear safety information and conduct documented follow-up via written or verbal communication with study sites, monitors, or partners.
- Monitor and manage the Clinical Safety mailbox daily to ensure timely receipt, acknowledgment, triage, and routing of safety information in compliance with regulatory timelines and internal procedures.
- Ensure all safety mailbox communications are appropriately documented, tracked, and actioned, including coordination of follow-up with study sites, partners, and internal functions.
- Serve as a pharmacovigilance liaison and resource to internal and external stakeholders, including Clinical Operations, Data Management, Quality Assurance, Safety Working Groups, and clinical sites, as delegated.
- Support Safety Working Group activities, including agenda preparation, material compilation, safety issue tracking, and documentation of discussions, decisions, and action items.
- Collaborate with Senior Clinical Safety Specialists to support reconciliation between clinical and safety databases and resolution of discrepancies in a timely and traceable manner.
- Support delivery of routine and ad hoc safety deliverables to pharmaceutical partners in accordance with applicable Safety Data Exchange Agreements and contractual timelines.
- Contribute to the preparation, review, and submission of safety sections of annual reports, regulatory filings, and other periodic safety deliverables, as assigned.
- Support audit and inspection readiness activities, including document preparation, response drafting, and implementation of follow-up actions under supervision.
- Maintain compliance with SOPs and Work Instructions. Identify and escalate process gaps, risks, or improvement opportunities to support a robust and sustainable safety operation.
- Participate in daily Clinical Safety team meetings to provide case status updates, flag risks or delays, align on priorities, and support timely decision-making and workload management.
- Perform other safety-related duties as assigned to support departmental objectives and operational continuity.
SKILLS/COMPETENCIES
- A minimum of a Bachelor’s degree in medicine, pharmacy, or other healthcare-related profession or biomedical sciences is required
- Up to six years of experience in drug safety/Pharmacovigilance in a pharmaceutical industry setting or the equivalent
- Understanding Pharmacovigilance-related regulations, GVP, and GCP is preferred
- Working knowledge of PV Systems, such as Oracle Argus Safety is required.
- Experience interacting with clinical third parties (e.g., clinical sites, independent DMCs) is preferred
- Proficient in Microsoft Office Suite (Word, Excel, and PowerPoint), Visio, email (Outlook), and SharePoint (or other management/shared content/workspace).
- Strong verbal, written, and interpersonal communication skills with study sites and internal staff.
- Excellent organization, prioritization, project management, and delegation skills, with strong attention to detail.
- Demonstrate ability to prepare for daily operational meetings with accurate status updates, clear questions, identified risks, and proposed solutions.
- Able to work collaboratively in a multidisciplinary team.
- Able to work extended and/or flexible schedules to meet deadlines.
Disclaimer: This job description is not intended to be an exhaustive list of all duties, responsibilities, or qualifications. Duties may change, or new responsibilities may be assigned at any time, with or without notice.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.