ClinChoice

Medical Reviewers Head- Pharmacovigilance

NEW YORK, NYPosted 30+ days ago

Job summary

  • Job post source

    This job is directly from ClinChoice

  • Job overview

    The Medical Reviewers Head- Pharmacovigilance leads the medical review team to ensure safety data compliance and patient safety in pharmacovigilance.

  • Responsibilities and impact

    The role involves managing the medical review team, overseeing safety data evaluation, ensuring regulatory compliance, collaborating with departments, providing medical expertise for safety assessments, and training team members.

  • Experience and skills

    Requires a medical degree with 5-10 years in pharmacovigilance including 3 years in leadership, strong regulatory knowledge, and expertise in medical evaluation of safety data.

  • Work environment and culture

    The position is full-time remote with flexible work options and occasional travel, fostering a collaborative and inclusive team culture.

  • Company information

    ClinChoice operates in pharmaceutical manufacturing focusing on safety and regulatory compliance in drug development.

  • Team overview

    The candidate will lead a team of medical reviewers within the pharmacovigilance safety department, working closely with cross-functional teams.

  • Job location and travel

    Remote with occasional travel required.

  • Unique job features

    The role offers leadership in pharmacovigilance safety with strategic input on regulatory submissions and safety signal detection.

Company overview

ClinChoice is a global clinical research organization that provides comprehensive clinical development and consulting services to the pharmaceutical, biotechnology, and medical device industries. They make money by offering services such as clinical trial management, regulatory consulting, data management, and biostatistics to support the development and approval of new medical products. Founded in 1995, ClinChoice has grown through strategic acquisitions and partnerships, expanding its global footprint and capabilities to deliver high-quality, cost-effective solutions for their clients.

How to land this job

  • Position your resume to highlight leadership experience in pharmacovigilance, emphasizing your ability to manage medical review teams and oversee safety data evaluations in compliance with global regulatory standards like FDA, EMA, and ICH.

  • Focus on showcasing expertise in medical evaluation, risk-benefit analysis, and your experience collaborating with cross-functional teams such as Clinical Development, Regulatory Affairs, and Medical Affairs, as these are critical for this role.

  • Apply through multiple channels including ClinChoice's corporate career site and LinkedIn to maximize your application visibility and increase your chances of being noticed.

  • Connect with current ClinChoice employees in the Safety or Pharmacovigilance divisions on LinkedIn to gather insights about the role; use ice breakers like commenting on recent safety initiatives ClinChoice has undertaken or asking about their experience working remotely in this department.

  • Optimize your resume for ATS by incorporating keywords from the job description such as 'pharmacovigilance,' 'medical review,' 'risk-benefit analysis,' 'regulatory compliance,' and 'team leadership' to ensure it passes automated screenings effectively.

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