Job Summary :
We are seeking a highly skilled Clinical Trials Specialist to join our team. The ideal candidate will have expertise in conducting clinical trials, managing trial protocols, and collaborating with clinicians and research partners.
Key Responsibilities :
- Clinical Trial Conduct : Design, manage, and conduct clinical trials ensuring compliance with ethics and regulations.
- Protocol Management : Develop and implement clinical trial protocols, including obtaining IRB / ethics approvals and regulatory pathways.
- Collaboration : Work closely with hospitals, clinicians, and research partners to ensure successful patient trials.
- Certification : Assist in medical device certification ISO 13485 IEC 60601 CE FDA CDSCO etc.
- Data Analysis : Analyze clinical data, prepare validation reports, and publish papers in peer-reviewed journals or conferences.
Requirements :
Education : Degree in Medicine MBBS / MD / Physio OR Biomedical Engineering / Science.Experience : Prior experience with medical devices or clinical research is required.Skillset : Knowledge of clinical trial protocols, IRB / ethics approvals, and regulatory pathways is essential.Passion : Strong interest in AI / healthcare technology and ability to contribute to research papers and publications.Nice to Have :
Hands-on Experience : Hands-on experience with medical device certifications ISO CE FDA.Digital Health : Prior work in digital health wearables or AI-powered devices is desirable.Publications : Publications in peer-reviewed journals or conferences are an added advantage.What We Offer :
This role offers the opportunity to bridge medicine and research, bringing innovative healthcare products to patients.
About the Role :
This position requires strong analytical and communication skills, as well as the ability to work collaboratively with cross-functional teams.