Medical Advisor

Whiteice Network was established in April 2004 through an idea sharing a common vision of enhancing net worth of business services in Overseas and Domestic Recruitment Services. The path chosen was to not only offer and ensure high quality business services but also to have wide range scalability for the services.
- We would like to take this opportunity to introduce
- **Whiteice Network** |
- **360°**
**Recruitment Service Provider** as an emerging Recruitment Company based at
- **Ahmedabad - INDIA**.

We have a position matching your profile. Requirement is as follow.**Medical Advisor**
- **WNTMA20072023**
- Provide medical and scientific insights to support product development, clinical trial design, and regulatory strategy.
- Collaborate with the clinical research team to design and implement clinical trials, ensuring protocol development and patient selection criteria.
- Oversee the safety and well-being of participants in various study projects as the Medical Monitor.
- Review adverse event reports, safety data, and protocol compliance to ensure participant safety.
- Stay up-to-date with the latest developments in digital therapeutics, medical technology, and relevant therapeutic areas.
- Work closely with cross-functional teams to translate medical insights into user-friendly and impactful digital therapeutic interventions.
- Collaborate with regulatory affairs to ensure compliance with applicable regulations.
- Participate in interactions with regulatory authorities to address medical and scientific queries.
- Support the development of scientific content, educational materials, and training programs for healthcare professionals.
- Contribute to the interpretation and analysis of study results, preparation of clinical study reports, and regulatory submissions.

**Medical and Scientific Expertise**
- Stay up-to-date with the latest developments in digital therapeutics, medical technology, and relevant therapeutic areas.
- Provide medical and scientific insights to support product development, clinical trial design, and regulatory strategy.
- Conduct literature reviews, analyze clinical data, and contribute to the generation of scientific evidence supporting the efficacy and safety of our digital therapeutic products.

**Clinical Research Support**
- Collaborate with the clinical research team to design and implement clinical trials, including protocol development, patient selection criteria, and outcome measures.
- Monitor ongoing clinical trials, review data, and contribute to the interpretation and analysis of study results.
- Assist in the preparation of clinical study reports, manuscripts, and regulatory submissions.

Medical Monitoring- Serve as the Medical Monitor for various study projects, overseeing the safety and well
- being of participants.
- Review and evaluate adverse event reports, safety data, and protocol compliance to ensure participant safety.
- Collaborate with the clinical research team and investigators to address medical queries, protocol deviations, and safety concerns.

Regulatory Compliance- Stay informed about relevant regulatory guidelines and requirements, ensuring our products adhere to applicable regulations.
- Market Surveillance Reports.
- Participate in interactions with regulatory authorities to address medical and scientific queries related to our digital therapeutic products.

Cross-Functional Collaboration- Work closely with product management, software engineering, and user experience teams to translate medical insights into user-friendly and clinically impactful digital therapeutic interventions.
- Collaborate with the marketing team to develop scientific content, educational materials, and training programs for healthcare professionals.
- Support the commercial team in interactions with key opinion leaders, healthcare providers, and external stakeholders, providing medical expertise and insights.

**Key Skills**
- Strong knowledge of clinical trial design, data analysis, and interpretation of medical literature.
- Familiarity with regulatory requirements for medical devices, digital health products, or pharmaceuticals is highly desirable.
- Experience in medical monitoring, pharmacovigilance, or clinical safety oversight.
- Excellent communication skills, with the ability to present complex medical information effectively.
- Strong analytical and critical thinking abilities, with attention to detail.
- Collaborative mindset, capable of working in a fast-paced, dynamic environment.

**Salary**
- ₹100000/- to ₹125000/- pm

**Industry**
- HealthTech Industry

**Age Limit**
- Maximum 55 Years

**Education**
- **Medical Degree (MD) / Equivalent Qualification **specializing in a

**Experience**
- Minimum 4 to 7 Years of experience as a
**Medical Advisor /**
**Equivalent**
**Prior Experience** in
**Medical Affairs, clinical research, or regulatory affairs** within the
**Pharmaceutical / Biotechnology / Digital Health Industry**
**on Priority...**

**Location**
-