Clinical Research Specialist

2 days ago


Tirupati, Andhra Pradesh, India beBeeScientist Full time ₹ 60,00,000 - ₹ 1,20,00,000
Job Opportunity

We are seeking a skilled professional to develop high-quality clinical trial documents and translate complex scientific data into clear, regulatory compliant documents that support drug development and approval processes.

Key Responsibilities:
  • Develop protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs) in accordance with regulatory guidelines.
  • Translate complex scientific data into clear, concise language that supports the success of clinical research and regulatory submissions.
  • Craft abstracts and manuscripts that demonstrate strong scientific communication skills.
  • Collaborate with cross-functional teams to ensure effective and complete documentation within timelines.

Requirements:

  • Proficiency in developing high-quality clinical trial documents.
  • Strong scientific writing and communication skills.
  • Ability to work collaboratively as part of a team.
  • Experience in crafting abstracts and manuscripts.

Preferred Qualifications:

  • Masters or Ph.D. in Life Sciences or related field.
  • Minimum 3-5 years of experience in clinical research or medical writing.

Company Overview:

Our organization is a leading provider of cutting-edge technology solutions. We value innovation, teamwork, and customer satisfaction.

As a member of our team, you will have opportunities for growth and professional development in a dynamic work environment.



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