TalentBurst, Inc.
TalentBurst, Inc.Verified Source

Drug Safety Coordinator TalentBurst Inc Raleigh NC

Onsite · Raleigh, North Carolina
Posted August 12, 2026
payroll

Overview

The independent Drug Safety Coordinator at TalentBurst, Inc. will efficiently accomplish drug safety tasks with minimal oversight. This role supports the Global Drug Safety team while collaborating across departments. Candidates should possess ARGUS safety database experience.

What You'll Do9

  • 1Identify track and file potential adverse event information
  • 2Monitor incoming information and assemble data for team meetings
  • 3Enter reports into tracking logs and create case folders
  • 4Delete confidential patient information from source documents
  • 5Record protocol and site numbers on source documents
  • 6Provide completed reports to case owners
  • 7Review source documents for AE completeness and determine follow-up needs
  • 8Maintain understanding of protocol scope and GCP guidelines
  • 9Manage receipt review and filing of literature sources containing AE information

Requirements3

  • 1Associate degree
  • 22-3 years recent clinical experience or equivalent training
  • 3Clinical drug development experience preferred

Salary Insight

Salary not disclosed in listing

Location

Typeonsite
LocationRaleigh, North Carolina

Required Skills

ARGUSsafety databaseGood Clinical Practices (GCP)regulatory guidelinesmedical terminologyinterpersonal skillsorganizational skillsprioritization skillsmultitaskingcomputer literacy
Share:

Similar open positions

Explore active roles that match your skills and interests.

Connexion Systems & Engineering, Inc.

16h agoRaleigh, North Carolinapayroll

Drug Safety Coordinator, Pharmacovigilance & Clinical Research

You will own adverse event intake, processing, and documentation for a clinical research program. Use ARGUS or other safety databases to track and file AE reports. Work within a team of Drug Safety Scientists and cross-functional partners. Maintain compliance with GCP and regulatory standards. This role offers direct impact on patient safety in a regulated environment.

40K–54K
argusgcpadverse event reporting+2 more

Actalent

11h agoRaleigh, North Carolinapayroll

Drug Safety Associate, Pharmacovigilance

You will own adverse event processing within a global pharmacovigilance team, handling data from clinical trials and post-market sources. You operate in ARGUS and ensure GCP compliance while supporting safety evaluations. You collaborate with Drug Safety Scientists and cross-functional teams at a hybrid facility in Cary, NC. This contract role offers exposure to advanced biopharma technologies and professional growth in the Research Triangle.

Competitive salary
argusgcpclinical trials+2 more
Talent Groups

Talent Groups

16h agoBoston, Massachusettspayroll

Drug Safety Specialist

Lead independent pharmacovigilance professionals to own end-to-end adverse event case processing for marketed and investigational drugs. Manage regulatory compliance across FDA ICH and Google Cloud Platform standards while collaborating with cross-functional teams and CROs. Drive improvements in safety reporting efficiency and quality.

45K–50K
pharmacovigilanceadverse event case processingFDA regulations+5 more

AA2IT

11h agoRaleigh, North Carolinapayroll

Pharmacovigilance Specialist, Drug Safety & Medical Devices

You will own adverse event processing and regulatory reporting for all Merz Aesthetics products, including medical devices, cosmetics, and OTCs. You will ensure FDA and EU compliance for both marketed and investigational products, handling SAEs, AEIs, and pregnancy reports. You will work with clinical teams to develop safety sections for protocols and Investigator Brochures. You will use validated safety databases like Argus and ARISg to submit cases to worldwide agencies. This role offers a hybrid schedule with 3 days onsite and 2 days remote.

83K–87K
argusarisgmeddra+2 more

YO AI Labs

11h agoRemotepayroll

Pharmacovigilance Expert, Drug Safety & Regulatory Compliance

You will own the safety signal evaluation and regulatory documentation for an AI-driven healthcare project. Work with a cross-functional team of data scientists and clinicians to review, evaluate, and refine DSURs, PSURs/PBRERs, and safety data. No prior AI experience is required, but your expertise in GVP guidelines and ICH E2F/E2C(R2) standards will drive accurate, compliant content. This remote contractor role lets you apply your drug safety knowledge to shape next-generation AI tools while maintaining the highest quality standards.

146K–166K
pharmacovigilancedrug safetyich e2f+2 more

YO AI Labs

16h agoRemotepayroll

Pharmacovigilance Expert, Drug Safety & Regulatory Compliance

You will own pharmacovigilance documentation for AI-driven healthcare systems, reviewing DSURs, PSURs/PBRERs, and safety data to ensure regulatory compliance. Collaborate with a cross-functional team of safety scientists and engineers to refine AI evaluation tasks. This role stands apart by offering remote flexibility and no prior AI experience requirement, focusing purely on your drug safety expertise.

146K–166K
pharmacovigilancedsurpsur+2 more