[Hiring] Clinical Medical Services Specialist III @Mindlance

Role Description

This role is crucial for maintaining compliance with global regulatory standards and ensuring the highest quality of adverse event management.

• Collect, assess, and process adverse event information (both clinical and post-marketing) in a compliant and timely manner to adhere to global regulations.
• Seriousness assessment
• Labeling
• Causality determination
• Initial and follow-up evaluations
• Ensure adherence to company standards for quality, compliance, and productivity.
• Stay updated on the knowledge and skills required for effective case processing.

Qualifications

• Minimum qualification: 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 even if they lack the appropriate degree.
• Required experience: 2-4 years of clinical experience, or 2-3 years of clinical experience combined with 1-year of Pharmacovigilance experience.
• Essential knowledge: Familiarity with industry regulations such as ICH, FDA, EMEA, and MHRA.
• Competency: Proficiency in case processing processes, procedures, and conventions.

Requirements

• Pharma experience with clinical case processing is a must have.
• Veeva experience is not a must but would be very beneficial for the candidate to have.

Company Description

• Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.