RESPONSIBILITIES :  - Primarily serves as Global Medical Advisor on assigned projects.  - Serves as Scientific Advisor and provides guidance to Project Leaders on the medical and scientific aspects of assigned projects.  - Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility.  - Performs medical review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs).  -Provides therapeutic area/indication training for the project clinical team.  - Attends and presents at Investigator Meetings.  - Performs review and clarification of trial-related Adverse Events (AEs).  - May perform medical case review of Serious Adverse Events (SAEs), including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department.  - May provide medical support for the Analysis of Similar Events (AOSE), in collaboration with or on behalf of Pharmacovigilance department.  - May perform medical review of adverse event coding.  - Performs review of the Clinical Study Report (CSR) and patient narratives.  - Attends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.  STRATEGY :  - Provides expert advises to the development of medically sounded delivery strategies for small to large and/or complex multi-region studies in partnership with sales and other functions responsible for business development activities.  - Responsible for the development of the medically related aspects of client proposals including the budget related to medical monitoring.  - Provides medical and scientific advises to key internal stakeholders developing proposals: this may include, but is not limited to, reviewing the protocol for scientific/regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.  - Attends and presents at bid defense meeting, as required.  - Participates in strategic business development activities including presentations to prospective clients.  - Maintains awareness of industry development and may author related publications.  - May serve as Regional/Multiregional/Global Therapeutic Lead for specific indication(s).  REQUIRED KNOWLEDGE, SKILLS AND ABILITIES :  - Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in applicable therapeutic area.  - Knowledge of applicable local regulations and guidelines pertaining to clinical research.  - Strong communication, presentation and interpersonal skills, including good command of English language (both written and spoken).  - Ability to establish and maintain effective working relationships with coworkers, managers and clients.  - Proven skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility.  MINIMUM REQUIRED EDUCATION AND EXPERIENCE :  - A medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education, along with a medical license, or equivalent, from the country or region in which he/she resides and works is required, plus a minimum of 5 years' experience in clinical medicine. Preferably MBBS, MD both  SALARY : Best in the industry

Delhi NCR

Associate Director - Medical Affairs - Diabetes 

Associate Director - Medical Affairs - Diabetes  ,Job Description for Associate Director - Medical Affairs - Diabetes  in ProEdge in  Delhi NCR for (5-15) years of experience. Apply Now!

Job Description for Associate Director - Medical Affairs - Diabetes  in ProEdge in  Delhi NCR for (5-15) years of experience. Apply Now!