Clinical Trial Registration Specialist

1 - 4 years

6 - 9 Lacs

Posted:2 days ago| Platform: Naukri logo

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Work Mode

Work from Office

Job Type

Full Time

Job Description

  • Prepare and submit clinical trials to public registries such as Clinicaltrials.gov and EU PAS.
  • Collaborate with cross-functional teams to ensure accurate and timely trial registrations.
  • Develop and maintain expertise in clinical trial regulations and guidelines.
  • Conduct thorough reviews of clinical trial applications to ensure compliance.
  • Provide training and support to internal stakeholders on clinical trial registration processes.
  • Stay up-to-date with changes in clinical trial regulations and industry trends.
Job Requirements
  • Bachelor's degree in Science (B.Sc) or equivalent.
  • Minimum 3 years of experience in clinical trial registration, quality assurance, or regulatory affairs.
  • Strong knowledge of clinical trial regulations and guidelines.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and collaboratively within a team environment.
  • Proficient in Excel and analytical skills.
  • Demonstrated ability to work independently and seek out support when needed.
  • Written and oral communication skills.
  • Strong organizational skills with the ability to multitask and prioritize, and take on new initiatives and improvement efforts.
About Company
Bristlecone is a leading biopharmaceutical company committed to transforming patients' lives through science. We offer a dynamic and supportive work environment that fosters growth and development.

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Bristol Myers Squibb logo
Bristol Myers Squibb

Pharmaceutical Manufacturing

Lawrence Township NJ

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