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Regional Medical Advisor

3.00 to 5.00 Years   Ahmedabad   29 Jun, 2019
Job LocationAhmedabad
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaMedical Transcription
EmploymentTypeFull-time

Job Description

  • The RMA (Regional Medical advisor) is a credible and valued representative of the company in field to interact with key stakeholders across their regions/products/TAs to establish and maintain scientific relationships with opinion leaders and other healthcare professionals via scientific approach that is aligned with the Brand Team objectives and therapeutic area Medical Plan.
  • The RMA is responsible for providing a variety of external and internal customers with medical and scientific information on the appropriate utilization of specific company products and with more general information about their therapeutic area and disease state.
  • The RMA attends conferences and meetings on behalf of the company as scientific expert and serve as support to the field based sales team within a defined region
  • KEY ACCOUNTABILITIES:
  • Identify, establish and maintain collaborative relationships with KOLs, investigators and institutions strategic to expand research, advisory, and educational partnership opportunities and the effective use of company products.
  • Provide stakeholders with credible, fair balanced, scientific information in assigned disease areas.
  • Obtain feedback and advice about company products or pipeline through various interactions and communicate relevant information back to internal stakeholders.
  • Collect, analyze, and communicate fair-balanced information concerning therapeutic area, treatment options, emerging standards of care, and competitive intelligence, reviews scientific publications and address medical information inquires
  • Provide effective clinical presentations to internal and external audiences and tailors presentations to meet specific audience needs
  • Conduct local scientific educational programs that aim to satisfy the specific scientific needs of individual KOLs and Institutions
  • Provide clinical input to the regulatory affairs department in the preparation of regulatory submissions and product registrations.
  • Provide clinical support to manufacturing and quality for sustaining commercial products; e.g. resolution of quality concerns, evaluation of customer complaints
  • Assist in protocol development, site selection, recruitment strategies, clinical operations collaboration, and communication with the Brand team and the Medical Advisor
  • To act in accordance with the local Country legislation
  • Dispose of all rights to the srvice works created during the execution of the employment contract, including , but not limited to , the rights to computer software ( including software and object codes and other elements , without which the work and / or modification of these programs is difficult or possible) , other aspects of copyright.
  • Regularly review corporate e-mail to ensure the timely response within the powers granted in accordance with this instruction, requests , tasks and orders coming from both the Companys employees and third-party organizations.
  • Timely and accurately performs oral and written housekeeping tasks and assignments of their leader and the Companys management. Correspondence by electronic means (fax, e-mail, etc.) is equivalent to writing correspondence. Service tasks and assignments, thus obtained, are binding.
  • Respond to requests from employees of the Company in the manner and within the competence of its officers.
  • Do not make on behalf of the Company any public statements, representations, including written, does not provide statements, except separately agreed in writing with the head of the Department of Communications, or cases.
  • It is mandatory to regularly attend events held on behalf of the Companys management, as well as training and briefings related to the employee.
  • Passes the annual and semi-annual evaluation of the fills and sends to the Department of Human Resources required documents in the prescribed form and the Company no later than the dates indicated in official emails from the Department of Human Resources of the Company.
  • Confirms in writing his/her introduction to the newly created and the current laws of the Company, wearing an obligatory nature, in the terms established by the Companys management.
  • For proper and efficient performance of duties on behalf of the Company on official travel.
  • Knows and complies with the requirements of the current legislation, in particular the requirements of legislative acts listed in the documents regulating the activities of this job description.
  • Comply with the applicable local regulations Companies, orders, regulations, instructions, policies, procedures, rules and other documents bearing the obligatory character, regardless of their shape, which is familiar for his signature or by reading the corporate e-mail.
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Keyskills :
managementintelligencerecruitmentresearchadvisorytrainingsoftwaremailmanufacturingcorrespondenceompetitiveregulatoryaffairs

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