Job Description

Coordinate and manage clinical studies, ensuring compliance with regulatory policies.

Maintain study documents and records.

Assist Principal Investigator with training materials and ensure all team members meet training requirements.

Collaborate on regulatory submissions and audit responses.

Prepare study materials, including consent forms, CRFs, and logs.

Establish and organize study files.

Communicate study requirements and progress to all stakeholders.

Ensure adherence to SOPs and Good Clinical Practices.

Protect data integrity and patient safety.

Qualifications:

Education: BSc/Msc in Life Science/B. Pharm. with PGDCR/Certification in Clinical Research/BHMS/BAMS/MBBS/PhD/MPH/M.Pharm/ Pharma D

Experience: Minimum of 1 years of professional experience in managing clinical research.

Location: Mumbai, Maharashtra

Eligibility Criteria

Not Specified

Desired Candidate Profile

Graduation - Graduate-Other

Organization Details

• Organization Name:Hematology Cancer Consortium Association
• About Organization:Hematology Cancer Consortium (HCC), is a multi-center collaborative academic organization established with the aim to improve knowledge, standardize cost-effective treatment strategies and promote regionally relevant research in hematological cancers.
  
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