Senior Pharmacovigilance Data Collection Specialist

2 days ago

Hyderabad Secunderabad Telangana, India beBeeCompliance Full time

In this key role, you will be responsible for developing and executing a comprehensive strategy for safety-related data collection in clinical trials.

This will involve collaborating closely with cross-functional teams to ensure standardization and regulatory compliance across various programs.

Key Responsibilities:
  • Develop and execute the safety data collection strategy for clinical trials.
  • Review, approve, and implement the safety data collection strategy across multiple programs.
  • Collaborate with cross-functional teams to ensure compliance with pharmacovigilance standards and operational consistency.
Requirements:
  • Masters degree OR
  • Bachelors degree with 2 years of pharmaceutical industry experience OR
  • Associate's degree with 6 years of pharmaceutical industry experience OR
  • High school diploma / GED with 8 years of pharmaceutical industry experience.
Preferred Qualifications:
  • Strong analytical skills to resolve day-to-day challenges effectively.
  • Ability to apply a methodical approach to completing tasks and solving problems.
  • Solid written and oral communication skills; ability to clearly present information and actively listen at various organizational levels.
  • Ability to work independently with minimal supervision while also being a collaborative team player.
  • Demonstrated ability to learn quickly and adapt to new systems, processes, and tools.
  • Highly organized, reliable, and responsive with attention to detail.
What We Offer:
  • A unique opportunity to make a significant impact on the safety and compliance of global clinical trials.
  • A collaborative environment that fosters growth and innovation within the pharmaceutical industry.
  • Competitive compensation with opportunities for career advancement.
  • A comprehensive benefits package designed to prioritize employee well-being.

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