Clinical Trial Physician

2 days ago

Ahmedabad, Gujarat, India Theia New Consultancy Full time ₹ 12,00,000 - ₹ 36,00,000 per year

The Clinical Trial Physician is responsible for providing medical input within the organization as well as to external partners and performing medical review tasks within the context of clinical trials. Furthermore, the Clinical Trial Physician is responsible for undertaking scientific/medical writing tasks within the organization.

Role & responsibilities

Is responsible for the development of:

  • All study related documents that fall under the Clinical Science Department scope (e.g., Study Protocols, ICFs - in collaboration with other departments e.g., Clinical Operations, Regulatory, as required -, Pharmacy Manuals, Medical Review Plans, etc.),
  • Scientific presentations and manuscripts,

  • Medical training material (i.e. therapeutic area and study protocol training material)

  • Delivers internal and external study protocol and therapeutic area training courses

  • Provides medical expertise and consultation within the Company on key therapeutic areas of the clinical development program
  • Provides guidance to all involved departments on the medical and scientific aspects of the assigned clinical trials/projects.
  • Responds to medical queries from all involved parties in assigned clinical trials (e.g., CRAs, Project Managers, Clinical Operations Managers, Investigators) and collaborates with all concerned staff in maintaining an up-to-date study-specific Q&A log
  • Is available 24/7 to respond to urgent medical/protocol related issues derived from an Investigational Site, as applicable
  • Performs periodic medical review of the data from clinical trials according to the study-specific Medical Review Plan requirements (e.g., review of eligibility, review of efficacy and safety data).
  • Performs real-time medical review on urgent medical and safety issues, as needed
  • Collaborates with and provides medical input to the Data Management staff to ensure the successful development of the study-specific eCRF
  • Attends Investigator Meetings and Conferences, as applicable
  • Complies with the Company's Quality and Information Security Management Systems and applicable national and international legislation, including legislation for data protection and ICH GCP requirements

Preferred candidate profile

  • Required Medical Degree (MBBS, MD)
  • Preferred: Clinical experience in the therapeutic area of the assigned study or of the Companys clinical development program - Preferred: 2 years of experience in a CRO or in the pharma industry in a relevant role (Clinical, Medical Information, Medical Affairs or PV)

Key competencies

  • Exceptional written and oral use of English
  • In-depth knowledge of medical and drug terminology
  • Good medical judgement and ability to make medical decisions
  • Excellent communication skills
  • Excellent business acumen
  • Initiative taking and team working attitude
  • Excellent Organizational skills
  • Innovative thinking
  • Excellent IT skills
  • Deep understanding of the Clinical Development industry

  • Clinical Trial Assistant

    2 weeks ago

    Ahmedabad, Gujarat, India HREE Research Pvt Ltd Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    Company DescriptionHREE Research Pvt. Ltd. is a full-service Clinical Research Organization (CRO) offering comprehensive, end-to-end clinical research solutions. We specialize in supporting pharmaceutical, biotechnology, and medical device companies across all phases of clinical trials. Our services include study design and protocol development, regulatory...

  • Clinical Trial Operations

    2 weeks ago

    Ahmedabad, Gujarat, India Morgan Placement Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    Job Title: AGM / DGM – Clinical Trials (Protocol & Report Writing)Department: Clinical Research / Clinical OperationsMinimum 10–15 yrs of relevant experience in clinical trials, protocol writing, CSR writing, and regulatory documentation

  • Clinical Research Physician

    2 weeks ago

    Ahmedabad, Gujarat, India Vgcro Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    Responsibilities:Conduct clinical trials with precisionManage clinical data accuratelyCollaborate on drug safety initiativesEnsure compliance with regulatory standardsMonitor adverse events promptly

  • Clinical Compliance Specialist

    1 week ago

    Ahmedabad, Gujarat, India beBeeCompliance Full time ₹ 20,00,000 - ₹ 25,00,000

    Clinical Quality Assurance SpecialistThe Role:This position will oversee end-to-end clinical trial activities from a quality perspective.Oversight of Clinical Trial Medical Science, Operations, and Clinical Data Management teams' quality compliance.Review of study-related activities, processes, procedures, and adherence to applicable regulations and...

  • Clinical Affairs Lead

    2 weeks ago

    Ahmedabad, Gujarat, India Zydus Group Full time ₹ 15,00,000 - ₹ 20,00,000 per year

    Position- Lead - Clinicals AffairsCompany:Zydus Medtech Pvt LtdReporting:Zydus Medtech HeadLocation:AhmedabadKey ResponsibilitiesThe Lead of Clinical Affairs will lead the strategic planning, execution, and oversight of all clinical research and evaluation activities across Zydus Medtech's medical device portfolio. This role ensures that clinical evidence...

  • Clinical Affairs Lead

    2 weeks ago

    Ahmedabad, Gujarat, India Zydus Group Full time

    Position - Lead - Clinicals Affairs Company: Zydus Medtech Pvt Ltd Reporting: Zydus Medtech Head Location: Ahmedabad Key Responsibilities The Lead of Clinical Affairs will lead the strategic planning, execution, and oversight of all clinical research and evaluation activities across Zydus Medtech's medical device portfolio. This role ensures that...

  • Clinical Affairs Lead

    1 week ago

    Ahmedabad, Gujarat, India Zydus Group Full time

    Position - Lead - Clinicals AffairsCompany: Zydus Medtech Pvt LtdReporting: Zydus Medtech HeadLocation: AhmedabadKey ResponsibilitiesThe Lead of Clinical Affairs will lead the strategic planning, execution, and oversight of all clinical research and evaluation activities across Zydus Medtech's medical device portfolio. This role ensures that clinical...

  • Clinical Affairs Lead

    7 days ago

    Ahmedabad, Gujarat, India Zydus Group Full time

    Position - Lead - Clinicals AffairsCompany: Zydus Medtech Pvt LtdReporting: Zydus Medtech HeadLocation: AhmedabadKey ResponsibilitiesThe Lead of Clinical Affairs will lead the strategic planning, execution, and oversight of all clinical research and evaluation activities across Zydus Medtech's medical device portfolio. This role ensures that clinical...

  • Clinical Research Associate

    1 week ago

    Ahmedabad, Gujarat, India Sterling Accuris Wellness Full time ₹ 4,00,000 - ₹ 8,00,000 per year

    About the Role:Key role as a project manager would be Single Point of Contact (SPOC) for the Sponsor from Sterling Accuris Wellness Pvt. Ltd. for laboratory testing and the associate services for clinical trials.The role will require the ability to support the clinical trial study pipeline which could include various projects covering various therapeutic...

  • Global Clinical Affairs Director

    1 week ago

    Ahmedabad, Gujarat, India beBeeClinicalAffairs Full time ₹ 2,22,12,000 - ₹ 2,59,40,000

    Clinical Affairs LeadThe Clinical Affairs Lead is a strategic and collaborative role that drives the planning, execution, and oversight of all clinical research and evaluation activities across medical device portfolios. This position ensures that clinical evidence supports product safety, efficacy, and regulatory compliance, while enabling innovation and...