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Jobs(31,339)/Community Lead Role(118)/Precision for Medicine (38) - Safety Lead
Precision for Medicine

Precision for Medicine - Safety Lead

Remote - USA$111k - $111k1mo ago
RemoteStaffNAPharmaceuticalsClinical ResearchCommunity LeadCROPharmacovigilanceReportingDocumentationProject PlanningClinical TrialsCRO

Requirements

• 10+ years clinical safety experience • 5+ years Pharmacovigilance (PV) experience • Health care professional • Hands on experience with global safety database(s), SAE case processing, and safety reports generation • Working knowledge of MedDRA and WHODrug • Working knowledge of FDA safety regulations, ICH guidelines, and Global regulations • Demonstrated knowledge of relevant regulatory agency(s) guidelines governing both Safety reporting and processing for clinical trial environments. • Demonstrated knowledge of supporting internal audits, inspection readiness and regulatory agency(s) inspection support for clinical trials including BLA or NDA approval inspections. • Excellent communication and analytical skills (written and oral). • Excellent judgment and ability to communicate complex clinical issues in a scientifically sound and understandable way. • Ability to work in a fast-paced, innovative environment while remaining flexible, proactive, resourceful, and efficient. • Preferred: • Nursing or pharmacy degree • Industry experience in CRO or pharmaceutical company • Project management experience • #LI-KH1 #LI-Remote

Responsibilities

• Essential functions of the job include but are not limited to: • Interfacing with sponsors, vendors, and other internal team members in the area of safety/PV to assist in the design and implementation of safety collection tools, processes, and reporting systems. • Participate in the assessment and set-up of a safety database to capture SAE data. • QC of documents and safety reports when needed. • Preparation and/or review of project specific safety reporting plans and medical coding plans • Preparation and/or review of safety training materials • Review of Safety related budget tasks and activities • Develop and manage standard operating procedures and work instructions. • Serve as subject matter expert for department. • Provide ongoing training and mentorship for Safety Specialists • Participate in audits and audit preparation, kick-off meetings, and investigator meetings. • Participate in the CAPA management process. • Participate in bid defenses for existing and potential clients. • Assist departmental management with resource management. • Assist departmental management with oversight. • Serve as project manager for safety standalone projects. • Lead departmental initiatives and cross-functional development activities. • Support the generation of SAE/AESI queries and tracking including oversight in the query resolution escalation efforts. • Provide input and review of responses to regulatory agency questions with regard to safety/ pharmacovigilance activities. • Assist clients and/or other departmental staff with safety-related reviews and other services.

Benefits

• Reasonable estimate of the current range • $110,700—$166,100 USD • Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

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