Senior Document Developer

5 days ago

Solapur, Maharashtra, India beBeeScientific Full time US$ 60,000 - US$ 85,000
Scientific Writer Opportunity

Key Role: Scientific Writer/Clinical Study Researcher

  • Develop high-quality clinical trial documents, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).
  • Translate complex scientific data into clear, regulatory compliant documents that support drug development and approval processes.
  • Craft abstracts and manuscripts, demonstrating strong scientific communication skills.
  • Deliver high-quality, accurate, and well-structured documents contributing to the success of clinical research and regulatory submissions.
  • Prepare protocols, CSRs, Patient Information Sheets (PIS-ICFs), and CRFs.
  • Understand study objectives and design protocols.
  • Review SOPs and communicate with stakeholders to ensure timely and effective documentation.
Essential Skills:
  • Strong writing and editing skills with experience in clinical research document development.
  • Excellent scientific knowledge with proficiency in translating complex data into clear documents.
  • Ability to work independently and collaboratively as part of a team.
  • Effective communication and stakeholder management skills.
  • Experience with regulatory compliance and quality assurance procedures.
Benefits:

• Work on diverse clinical research projects with opportunities for growth and professional development.
• Collaborate with experienced professionals in the field of clinical research.
• Develop expertise in clinical research documentation and scientific writing.

Other Requirements:

• Proficient in MS Office and Adobe Acrobat software.
• Strong analytical and problem-solving skills with attention to detail.

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