Job Description

Primary Job Function:
•    Supports Global Director Medical & Scientific affairs  to define medical affairs strategy and conduct medical activities related to IVDR process. .
Core Job Responsibilities:
Supports and conducts the following responsibilities under supervision of Global Director Medical & Scientific affairs:
•    Functions as a scientific / medical liaison to key stakeholders in the IVDR core team
•    Drives and generates medical actions  in order to resolve medical/scientific issues related to different IVDR actions require by the team.
•    Participate in all IVDR meeting in order to represent Medical Affairs functions and provide support for all medical need identify by the IVDR team. 
•    Review publish literature and real life publish evidence related to our products, analyze  and present in the format need, to support IVDR team to remediate needs.  
•    Collaborates on planning and execution of Advisory Board Meetings or other non-promotional medical projects in order to provide the medical evidence need it for IVDR process. 

•    Provides sound and up-to-dated medical information, disease knowledge and medical training when necessary to other business functions. 
•    Drives medical scientific knowledge, reviews medical literature, generates potential new different ideas to enhance and maximize potential benefit for disease management and patient care.  
•    Maintains all relevant documentation for medical affairs projects and activities for compliance, including related to IVDR process.

•    Contributes to medical education content generation for digital activities and platforms intended for patients and HCPs. 
•    Identifies & oversees establishment and maintenance of scientific collaborative relationships with Key Opinion Leaders (KOLs), accountable and responsible for KOL development, KOL engagement, and approaching KOLs for provision of services.

Minimum Education:
•    M.D. required

Minimum Experience/Training Preferred:
•    Good understanding and experience in the conduct of clinical trials or in medical research in the industry or academia or equivalent.
•     Minimum 3 years + of experience in related role in industry. 
•    Experience in seek medical information and write medical documents 
•    Prior experience in global medical affairs role is desirable.
•    Must have attention to detail, able to work in a team environment, good organizational skills, and multi- tasking ability.
•    Project management skills needed.
•    Strong written and verbal communication skills.
•    Strong presentation skills.

Pay ranges between $70-80/hr based on experience 

Job Tags

Contract work,

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