Job Description Role Overview:
/n We are seeking a skilled and experienced Clinical research Manager to lead the clinical study associated activities along with preparing the Clinical Documents efforts for non-active implantable medical devices. This role will also be responsible for guiding the team through design and develop clinical protocols and execute clinical studies (pre-market or post-market studies).
The candidate should have extensive experience in clinical evidence generation strategy and scope research topics to provide recommendations on clinical trial strategy. The ideal candidate will bring in-depth knowledge of international medical device clinical research expertise, robust scientific writing capabilities, and demonstrated experience in end-to-end clinical evaluation and evidence generation.
/n Key Responsibilities:
/n Clinical Evidence Development:
/n · Author and maintain high-quality clinical documents including CERs, CEPs, PMCFPs, PMCFRs, PMSP, PSURs, and SSCPs in line with EU MDR and other international standards.
/n · Conduct thorough risk–benefit analyses and integrate data from preclinical, clinical, and post-market sources.
/n Cross-functional Collaboration:
/n · Interface closely with R&D;, Clinical Affairs, Marketing, and Regulatory teams to access and identify the necessary preclinical, clinical and technical information.

/n · Develop clinical and marketing communication tools such as peer-reviewed manuscripts, white papers, one-pagers, slide decks, surgical techniques, and more.

/n Scientific Literature Research & Analysis: /n · Design robust and reproducible literature search strategies.





/n · Perform systematic literature reviews and create comprehensive State of the Art summaries across diverse indications and implant technologies.
/n · Critically appraise scientific literature and write clinical summaries to determine evidence gaps, assist in research and development of clinical strategies for clinical investigational protocols.
/n Clinical Study Documentation:

/n · Draft clinical trial protocols, ethics approval submissions, case report forms, informed consent documents, investigator brochures, clinical study reports, and support regulatory related submissions.

/n · Develop and manage clinical trial documentation: site master files, trial master files, Clinical trial logs, etc.
/n Clinical Operations & Oversight:
/n · Lead clinical budgeting and financial management, including preparation and negotiation of trial budgets, oversight of vendor contracts and clinical study agreements, management of investigator, and site payments.
/n · Oversee aspects of clinical operations, including monitoring visits, generation of reports, and coordination with third-party CROs and sites.
/n · Draft clinical study agreements, insurance documents, and ensure operational compliance across trial activities.
/n · Initiate, monitor and close-out clinical studies on study sites in accordance with applicable national and international regulations,



MDCGs, guidelines of ICH-GCP and NDCT-2019.
/n Regulatory & Compliance Frameworks:
/n · Ensure documentation aligns with latest MDR 2017/745 and relevant guidance (e.g., MEDDEV 2.7.1 Rev. 4, MDCGs, ISO 14155:2020, ISO 14971, ICH-GCP, etc.).
/n · Interpret and apply risk management standards and post-market surveillance frameworks, contributing to proactive safety strategies.
/n · Leading the team of clinical research and guiding Regulatory teams by providing inputs on intended use/clinical clinical research material preparation etc.
/n Essential Requirements:

/n · Domain Expertise: Proven experience in authoring regulatory and clinical documents for non-active implantable medical devices.

/n · Regulatory Acumen: Solid understanding of relevant global regulatory frameworks, especially EU MDR, MEDDEV, MDCG guidance documents, ISO standards, and ICH-GCP guidelines.

/n Core Competencies: /n · Risk–benefit analysis

/n · Scientific writing (CER, BER, PMCF, PSUR, SSCP, etc.)
/n · Managing and supporting clinical studies/trials on medical devices
/n · Clinical trial documentation & project coordination
/n · Literature review & data appraisal

/n · Cross-functional communication and stakeholder engagement

/n Required Knowledge of Guidelines and Standards: /n · EU MDR 2017/745

/n · MEDDEV 2.7.1 Rev. 04
/n · MEDDEV 2.12/2 Rev. 2
/n · MEDDEV 2.12/1
/n · MDCG 2020-5/6/7/8
/n · MDCG 2019-9 Rev.1
/n · ISO 14155:2020
/n · ICH-GCP
/n · Current Drugs and Clinical Trials Rules, 2019
/n · ISO 10993-1
/n · ISO 14971

/n · ISO 24971

📌 Clinical Research Manager (Surat)
🏢 CHETAN MEDITECH PRIVATE
📍 Surat