Clinical Trial Submission Expert

2 weeks ago

Hyderabad Secunderabad Telangana, India beBeeRegulatory Full time ₹ 15,00,000 - ₹ 28,00,000
Associate - Clinical Trial Submission Management

We are seeking a highly skilled and experienced professional to join our team in the role of Associate - Clinical Trial Submission Management. This position will be responsible for ensuring that clinical trial submissions are accurate, complete, and submitted in a timely manner.

The ideal candidate will have a strong understanding of regulatory requirements and guidelines, as well as excellent communication and organizational skills. They will also be able to work effectively in a team environment and prioritize tasks to meet deadlines.

Key Responsibilities:

  • Ensure accuracy and completeness of clinical trial submissions;
  • Develop and implement processes to improve efficiency and quality of submissions;
  • Collaborate with cross-functional teams to identify and resolve submission-related issues;
  • Provide training and support to colleagues on regulatory requirements and submission procedures;
  • Stay up-to-date with changes to regulatory requirements and industry standards.

Requirements:

  • Bachelor's degree or equivalent experience;
  • 0-3 years of experience in clinical trial management or a related field;
  • Strong understanding of regulatory requirements and guidelines;
  • Excellent communication and organizational skills;
  • Ability to work effectively in a team environment and prioritize tasks to meet deadlines.

Preferred Qualifications:

  • Practical experience with Veeva Vault;
  • Familiarity with global regulatory processes and standards;
  • Ability to quickly learn new software, regulations, and processes.

What We Offer:

Our company is committed to providing a supportive and inclusive work environment that allows our employees to grow and develop their careers. We offer competitive salaries, comprehensive benefits, and opportunities for professional growth and development.

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