Clinical Researcher Specialist

****If interested then kindly apply on below link****

https://noccarc.notion.site/clinicalresearcherspecialist

About Role:

To know more about Noccarc visit: www.noccarc.com

Noccarc office video: https://youtu.be/OoeD10ckrdU

Role:

Location:

Reporting To:

Mandatory Requirement:

Key Responsibilities:

(A) Product Definition & Development

• Provide clinical leadership by embedding frontline critical care expertise into product development.
• Work with product managers, system architects, and engineers to define clinical requirements, performance standards, and safety specifications for advanced critical care devices.
• Translate real-world ICU/OT workflows and customer pain points into evidence-based design inputs for product development.
• Guide the development of clinical algorithms, physiological models, and therapy workflows with engineering teams.
• Participate in risk assessment, usability analysis, and hazard evaluation from a clinical perspective.
• Provide structured clinical feedback during design reviews, prototyping, and verification phases to ensure alignment with international best practices.
• Support decision-making on trade-offs between usability, patient safety, clinical performance, and technical feasibility.

(B) Product Testing & Validation

• Design and coordinate ex-vivo, simulation, and clinical validation studies.
• Manage clinical validation/ trials, including protocol design, site selection, investigator coordination, and patient studies.
• Conduct comparative benchmarking of Noccarc devices with competitor products on performance, usability, and clinical outcomes.
• Prepare and maintain Clinical Evaluation Reports (CERs), Clinical Evaluation Plans (CEPs), and PMCF documents in compliance with EU MDR and other standards.
• Ensure validation data is scientifically robust and supports regulatory submissions.

(C) Medical Writing & Research Publications

• Author scientific papers, whitepapers, abstracts, and conference presentations in collaboration with hospitals and research partners.
• Write clinical manuals, usage guides, and training content for customers and internal teams.
• Contribute clinical documentation for regulatory submissions.

Requirements:

(A) Education

• MBBS degree (mandatory).
• Postgraduate degree in Critical Care, Anesthesiology, Pulmonology, or equivalent preferred.

(B) Experience

• 2+ years of ICU clinical experience in a reputed hospital (Mandatory)
• Prior exposure to clinical research, medical devices, is a plus.
• Experience in clinical trials, medical writing, or regulatory documentation (CER, CEP, PMCF) preferred.

(C) Skills

• Strong understanding of human physiology, respiratory therapy, and critical care workflows.
• Proficiency in interpreting clinical literature and writing scientific documents.
• Ability to define and evaluate product performance in real-world ICU settings.
• Strong communication skills with ability to influence both clinical and engineering teams.

Why Join Us?

• Work directly with the founders and R&D leads
• High ownership, fast learning curve, and direct impact on product outcomes
• ESOPs for high performers