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Scientist - Medical Affairs at ClinChoice. Location Information: USA. Job Title. Scientist, Medical Affairs. Department. Medical Affairs/Medical Affairs. Responsibilities. Primary Responsibilities:. ·       Effectively organize and delegate work where applicable to complete the assigned tasks to meet deadlines. ·       Mentor and bestow domain knowledge to the team.. ·       Ensure the assigned tasks are delivered 100% on time or before, as per project SLA or Internal set threshold. ·       Demonstrate Quality of Work & Commitment through excellence in work, ensure correctness and completeness in deliverables with minimum OR no re-work. ·       Be able to independently perform tasks with minimal guidance & supervision. ·       Functionally review the team’s work for accuracy and compliancee where applicable. ·       Ensure proper planning of the deliverable and foresee any risks that are likely to arise. ·       Ensure error free and 100% quality in assigned deliverables. ·       Ensure that all assigned goals [e.g. utilization and efficiency] are met as per set standards for the performance year. ·       Responsible to ensure training compliancee and timesheet compliancee. ·       Conduct functional training for the team members. ·       Support in the functional capability development of junior members. ·       Provides therapeutic area (e.g. Pain, Digestive Health, Smoking Cessation or UR/Allergy) knowledge support and clarification of science as needed and contributes to research activities via scientific publications.. ·       Conducts and evaluates literature searches and analyze scientific literature.. ·       Creates standard language for product information reference manuals including FAQs for new product launches, media issues, and publications.. ·       Provides medical support in reviewing the printed packaging components, labeling, and compendia.. ·       Collaborates with physicians as the medical representative on cross functional teams (copy clearance committees) to both marketed products and support to new marketed concepts for promotional and non-promotional pieces to ensure medical/scientific accuracy.. ·       Participates in creation of medical training materials and programs that are used to support initial and ongoing training for new employees.. ·       Trains employees who require in-depth scientific/medical knowledge of relevant products/therapeutic areas and in support of local and regional speakers upon solicited request.. ·       Creates and develops strategically targeted information in response to published scientific literature, news media releases, marketing initiatives, product recalls, or new or highly publicized medical discoveries or information.. ·       Assists in generating basic periodic or aggregate safety reports, regulatory submissions, PSURs, annual reports, CCDS.. ·       Supports Investigator initiated studies including correspondence with investigators, researching the investigator site and facilitating review and approval of IIS proposals. ·       Performs quality review of the Epidemiology authored sections of the RMP and provides feedback on quality assessment finding.. Secondary Responsibilities:. ·       Effectively organize work to complete the assigned tasks to meet deadlines. ·       Ensure the assigned tasks are delivered 100% on time or before. ·       Demonstrate Quality of Work & Commitment through excellence in work, ensure correctness and completeness in deliverables with minimum OR no re-work. ·       Support in review of work done by peer teammates, on need basis.. ·       Alerts and escalates to senior members as required, whenever project deliverable risks are visualized, OR issues encountered impacting the delivery schedule. ·       Ensure error free and acceptable quality in assigned deliverables. ·       Responsible to ensure training compliancee and timesheet compliancee. ·       Ensure that all assigned goals [e.g. utilization, quality and timeliness] are met as per set standards for the performance year. ·       Follow and comply with the Company’s Code of Conduct, Policies, and Procedures,. ·       Responsible for confidentiality, integrity, availability, and safeguarding of data,. ·       Responsible for reporting of security incidents and PIMS breaches as applicable,. ·       Comply with company QMS, ISMS and PIMS requirements and applicable regulatory requirements,. ·       Demonstrate adherence and compliancee to PIMS/GDPR requirements as follows: processed fairly, transparently, and lawfully; collected for specified and legitimate purposes; adequate, relevant, and limited to the specified purposes; processed in a secure manner. Skills and Qualifications. ·       Bachelor’s degree in science or above and in alignment with project /. business team requirements. PhD in Nutritional is preferred. ·       Minimum of 5 to 8 years of relevant experience in identified functional domain/ business workstream. #LI-PB1 #Remote