Clinical Research & Evidence Generation Executive

Location: Chennai | Travel: As required

Product: paceB, AI-Integrated Gait & Foot Function Analysis System

Role Overview The Clinical Research & Evidence Generation Executive is an individual contributor responsible for coordinating paceB studies from initiation through publication. The role manages sites, documentation, data workflows, scientific outputs, and translation of findings into Clinical, R&D;, and Product inputs. It has no people-management responsibility.

Key ResponsibilitiesClinical 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.

Compensation & Growth

· Competitive salary based on experience and capability.

· Chance to grow within Clinical Research and Clinical Affairs as the company scales.

📌 clinical research and Evidence Generation executive (Chennai)
🏢 Sone India Group of Industries
📍 Chennai