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Senior Research Document Specialist

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Agra, Uttar Pradesh, India beBeeClinical Full time ₹ 10,00,000 - ₹ 13,00,000
Job Title: Clinical Research Associate

About Us:

We are a global IT services company that partners with major firms in various industries. Our team combines deep industry expertise with agile development practices to deliver scalable and cost-effective digital transformation.

Key Responsibilities:

  • Author and analyze clinical trial documents, including protocols, informed consent forms, and clinical study reports.
  • Apply knowledge of clinical trial phases, study design, and drug development to create accurate and compliant documents.
  • Maintain compliance with global regulatory standards (FDA, EMA, ICH-GCP) and utilize medical terminologies and ontologies for clarity and consistency.
  • Collaborate with cross-functional teams to improve document accuracy and prompt effectiveness.

Required Skills: Protocol, Informed Consent Form (ICF), FDA, EMA, ICH-GCP

Experience: 1 - 5 years

Education Qualification: Any Graduation

Work Mode: Hybrid

Employment Type: Contract

Notice Period: Immediate - 15 Days

Interview Mode: 2 Rounds of Technical Interview

The ideal candidate will have strong analytical and communication skills, with the ability to work effectively in a team environment.

This role involves working on a wide range of projects, from initial concept to final delivery. You will be responsible for creating high-quality documents that meet our clients' needs and expectations. We are looking for someone who is able to work independently and as part of a team, with excellent communication and problem-solving skills.