What are the responsibilities and job description for the Drug Safety Specialist position at Talent Groups?
Hybrid Details: Onsite 3 days/week
Duration: 6 months to start
Job Description
The client is looking for a Drug Safety Specialist with 3 5 years of pharmacovigilance experience and a clinical background (e.g., RN, BSN, RPh, or PharmD) to support adverse event case processing for marketed and investigational products. This role is responsible for end-to-end safety case management, safety surveillance, vendor and cross-functional coordination, regulatory compliance, and clinical project support while ensuring adherence to FDA, ICH, GCP, and company pharmacovigilance requirements. Experience with oncology cases, safety databases such as Argus or ARISg, and regulatory safety reporting is highly preferred.
The Drug Safety Specialist will have primary responsibility for the following:
Case Processing (CT/ PM) - 50%
Duration: 6 months to start
Job Description
The client is looking for a Drug Safety Specialist with 3 5 years of pharmacovigilance experience and a clinical background (e.g., RN, BSN, RPh, or PharmD) to support adverse event case processing for marketed and investigational products. This role is responsible for end-to-end safety case management, safety surveillance, vendor and cross-functional coordination, regulatory compliance, and clinical project support while ensuring adherence to FDA, ICH, GCP, and company pharmacovigilance requirements. Experience with oncology cases, safety databases such as Argus or ARISg, and regulatory safety reporting is highly preferred.
The Drug Safety Specialist will have primary responsibility for the following:
Case Processing (CT/ PM) - 50%
- Responsible for the processing adverse event reports that include but not limited to the receipt, evaluation, reviewing and reporting of adverse event information for marketed and investigational products in accordance with ICH guidelines and applicable regulatory requirements including the FDA, SOPs, and applicable licensing or partnership agreements.
- Track cases from receipt to closure and work with clinical, regulatory, and contract research organizations (CROs) to ensure that all post-market and clinical safety pharmacovigilance activities are performed across ongoing projects independently.
- Perform verification of safety data and will utilize clinical judgement in coding of verbatim adverse events, medical history, and medications. Ability to synthesize complex clinical information into accurate and complete reports.
- Actively obtains follow-up through event resolution. Performs SAE reconciliation, ensuring completeness and closure of cases in a timely fashion.
- Performs continuous quality improvement initiatives to ensure data consistency across products and a high level of data quality.
- Contributes in the conduct of ongoing safety surveillance for marketed and investigational products. Assist with the identification and evaluation of events of special interests as well as aggregate data review.
- Acts as a safety representative and facilitator between external reporting sources such as call centers, CROs and investigator sites, interface with internal departments clinical operations, medical information, regulatory affairs, product development, quality assurance, biostatistics, data management, and legal.
- Participate in clinical project teams and other interdepartmental teams supporting clinical studies; reviews and provide comments on study related documents.
- Contributes to the development and writing of industry standard operating procedures and processes for pharmacovigilance activities including writing of the Safety Management Plan for assigned studies to ensure the uniform and timely processing of adverse event reports.
- Assist in responding to queries from health authorities or outside sources; Compiling and supplying as requested, safety information for Regulatory submissions such as IND (Investigational New Drug) safety reports, Annual Safety reports, PSUR, or clinical study reports.
- Other responsibilities as assigned
- A clinical degree (e.g., RPh/PharmD, BSN, RN)
- 3-5 years drug safety or clinical safety experience
- Two years clinical experience in a medical setting, demonstrate general medical and pharmacology knowledge
- Experience processing Oncology cases
- Have demonstrated knowledge of domestic and international regulatory safety reporting requirements, including FDA/ICH guidance related to pharmacovigilance and Good Clinical Practices
- Ability to make clinical decisions and formulate appropriate queries based on sound medical knowledge
- Competence with commercial safety application databases such as Clintrace, ArisG or Argus. Knowledge of clinical trial database (e.g., Trailmaster) is a plus
- Ability to work effectively as an individual contributor and as project team safety representative
- Is proactive, demonstrate ability to independently identify problems and effectively offer solutions
- The ability to work independently and multi-task with attention to detail,
- Excellent interpersonal, communication, and personal organization skills; ability to prioritize workload and work effectively, sometimes within resource constraints