Clinical Research & Evidence Generation Executive (Chennai)

Key Responsibilities

Clinical Research Coordination

• Support study feasibility, protocol development, ethics and institutional submissions, site onboarding, and initiation.
• Coordinate investigators, clinicians, research coordinators, and partner institutions; maintain study plans, documentation, actions, and milestone trackers.
• Keep studies on schedule by resolving or escalating site and internal dependencies.
• Travel to study sites for initiation, data-collection support, and investigator engagement as required.

Study Execution & Data Coordination

• Coordinate participant recruitment, study visits, device deployment, and protocol-compliant data collection.
• Support data-quality checks, query resolution, cleaning, reconciliation, dataset finalization, and inspection-ready records.
• Coordinate biostatisticians and other external specialists as required.

Scientific Writing & Publication Support

• Interpret study outputs and prepare abstracts, posters, presentations, and manuscripts.
• Coordinate manuscript drafting, author review, journal selection, submission, peer-review responses, revision, resubmission, and publication tracking.
• Identify and present relevant peer-reviewed publications, conference abstracts, posters, and oral or paper presentations.
• Maintain the paceB clinical evidence library and ensure authorship reflects substantive contribution, approval, and accountability.

Evidence Translation & Stakeholder Engagement

• Convert clinical findings and investigator feedback into documented R&D; and Product inputs, research gaps, and future-study opportunities.

Required Qualifications & Experience

• Bachelor's or Master's degree in Life Sciences, Biotechnology, Pharmacy, Physiotherapy, Biomedical Sciences, or a related discipline.
• 2-3 years of relevant experience in clinical or healthcare research, medical devices, CROs, hospitals, academia, or life sciences.
• Minimum two peer-reviewed research publications as an author or co-author are mandatory. Candidates must demonstrate meaningful involvement in study design, data acquisition, analysis, interpretation, manuscript drafting, or substantive scientific review, together with authorship-level approval and accountability.
• Preference will be given to candidates who have taken studies through data collection, cleaning or analysis, interpretation, manuscript preparation, journal submission, peer-review responses, revision, and publication.

Success Measures

• Studies delivered to milestone with complete documentation, reliable data, and timely query closure.
• Scientific outputs completed and submitted, with peer-reviewed publications accepted and published.
• Clinical findings converted into documented R&D; and Product inputs.