Freshers BSc Life Science Job Vacancies Latest at CLINICA Research
Job Role: Clinical Trial Assistant – Trainee
Company: CLINICA research
Location: Navi Mumbai
Qualification: Bachelor’s degree in life sciences or related field; or equivalent combination of education, training, and experience
Experience: 0–1 year
Salary: ₹20,000 per month
Essential Duties and Responsibilities:
• Act as a central contact for the clinical team for designated project communications, correspondence, and associated documentation.
• To assist the project teams with the set-up, organization, and maintenance of clinical study documentation (e.g. Study Files, CRFs, etc.) and guidelines (as appropriate) including preparation for internal/external audits, final reconciliation and archival.
• To assist in the processing of Data Collection Forms i.e. log in, tracking, quality control as appropriate for the study.
• To share responsibility in the quality control audits of clinical study documentation (e.g. Trial Master File, etc.) to ensure study files are inspection ready at all times.
• To assist with periodic review of study files for completeness.
• To assist project teams with trial progress tracking by updating the Clinical Trial. Management Systems/Study Tracking Tools.
• To assist in coordination of study related payments, if applicable.
• To contact and serve as a contact for clinical sites for basic requests (e.g., enrolment updates, missing documentation, meeting arrangements, etc.).
• To assist and attend the Project team with meeting coordination, activities preparation, generation of meeting minutes and agendas.
• To assist in the preparation of slides, as needed for project, departmental, sponsor presentations.
• To assist with the coordination of various tracking reports, including but not limited to, team member tracking and training.
• To work in collaboration with internal and external colleagues to meet project objectives and timelines.
• To Keep the Project Manager / Director-Operations/ Clinical Operations Designee informed of any issues within the Project Team which require attention.
• To maintain client confidentiality.
• Perform daily administrative activities, in conjunction with the Clinical Research Associates and other teams, to ensure a complete and accurate Trial Master File delivery.
• May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
• Any other activity or task as assigned by the Line Manager/Project Manager.
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