Clinical Medical Services Specialist III # 26-26670
US Tech Solutions•North Chicago, IL
About The Position
Collect, assess, and process clinical and post-marketing adverse event information in a compliant and timely manner in accordance with global regulations. Work includes seriousness assessment, labeling, causality determination, and initial and follow-up evaluations. Maintain adherence to company standards for quality, compliance, and productivity, and stay current on the knowledge and skills needed for effective case processing. This role supports compliance with global regulatory standards and high-quality adverse event management.
Requirements
- Bachelor's degree with a related health sciences background, such as RN, BSN, BS, or BS Pharm; candidates with previous pharmaceutical experience may also be considered without the appropriate degree.
- 2–4 years of clinical experience, or 2–3 years of clinical experience combined with 1 year of Pharmacovigilance experience.
- Familiarity with industry regulations such as ICH, FDA, EMEA, and MHRA.
- Proficiency in case processing processes, procedures, and conventions.
Responsibilities
- Collect, assess, and process clinical and post-marketing adverse event information in a compliant and timely manner.
- Perform seriousness assessments, labeling, causality determinations, and initial and follow-up evaluations.
- Adhere to company standards for quality, compliance, and productivity.
- Stay updated on knowledge and skills required for effective case processing.
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What This Job Offers
Career Level
Mid Level
