Senior Medical Affairs Manager - Pharma

<p style="text-align:inherit">&nbsp; &nbsp; &nbsp;</p><h2><b>JOB DESCRIPTION:</b></h2><p><b>PRIMARY OBJECTIVE:</b></p><p>The position represents the affiliate’s medical/ scientific voice of expertise for assigned relevant therapeutic areas and special task assignment.  The position provides medical / scientific expert advice / guidance to key customers for assigned products and relevant therapeutic areas, including scientific exchange and professional relationship development with key opinion leaders.  It provides medical / scientific input into marketing strategy and key commercial initiatives, as required, and medical / scientific support for medical department activities under the direction of the Head of the affiliate medical function.</p><p></p><p><b>CORE JOB RESPONSIBILITIES:</b></p><ul><li>Develop and maintain in depth knowledge for assigned product(s)/ relevant therapeutic area(s)</li><li>Provide expert medical/scientific advice for assigned products and related therapeutic areas</li><li>Provide medical/scientific input into marketing strategy and key commercial initiatives, as required. Deliver scientific and medical education programs to healthcare professionals</li><li>Review and approve promotional materials. Ensure that it is based on good clinical practice, is of the highest standards of medical accuracy and is fair, objective and balanced</li><li>Develop scientific material and initiates its request for approval</li><li>Co-operation on clinical research activities with the global and regional by taking responsibility for the implementation/ manage of local clinical trials, including IIS, BE, feasibility studies and non-interventional clinical research activities throughout project</li><li>Assures that clinical research program design meets scientific objectives and is aligned with our Medical Affairs Strategy</li><li>Ensure compliance with Corporate and Divisional Standard Operating Procedures SOPs, Good Clinical Practice, and local regulatory requirements pertaining to the conduct of clinical studies</li><li>Building relationships with Investigators and applying their inputs to enhance study design and protocols</li><li>Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas</li><li>Collaborate and liaise with study team members for project execution support as appropriate</li><li>Serves as scientific expertise on clinical research matters and govern regulatory requirements</li><li>Administer and maintain appropriate documentation such as protocol approval and related study expenditure to internal stakeholders</li><li>Accountable for supporting sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability</li><li>Manage internal TARC review and approval of local clinical activities in assigned therapeutic area(s)</li><li>Lead local clinical trial application through central research committee (if required)</li><li>Complete data entry to monthly metric</li><li>Manage CLIMATE and Clinical Tracker Sharepoint</li><li>Responsible and accountable for coaching and management of MA specialist performance including monitoring monthly metrics ensuring excellence in execution of his/her role towards achieving strategic and tactical Medical Affairs goals</li></ul><p></p><p><b>EDUCATION/QUALIFICATIONS/EXPERIENCE:</b></p><ul><li>Bachelor’s degree in a pharmacy plus a higher education in a master’s degree.</li><li>Minimum 2 years Medical Affairs Manager experience in pharmaceutical company</li><li>Excellent ability to prioritize and handle multiple tasks</li><li>Good project management, analytical, decision-making</li><li>General knowledge on drug development and clinical research an advantage</li><li>Keen interest in developing and maintaining expert knowledge for assigned therapeutic area/product and in medical research in general</li><li>Excellent communication skills including strong presentation skills</li><li>High customer orientation</li><li>Excellent skills to set stakeholders relationship, networking, tact and diplomacy</li><li>Fluent in English and Thai (both verbal and written)</li><li>Good computer skills and ability to learn and to adapt working with IT systems</li><li>Knowledge of ICH, GCP, regulations, industry practices and applicable standards</li><li>Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity</li><li>Willingness to travel upcountry and oversea</li></ul><p style="text-align:inherit">&nbsp; &nbsp; &nbsp;</p><p><b>The base pay for this position is </b></p>N/A<p style="text-align:left"><span>In specific locations, the pay range may vary from the range posted.</span></p><p style="text-align:inherit">     </p><h2><b>JOB FAMILY:</b></h2>Medical &amp; Scientific Affairs<p style="text-align:inherit">&nbsp; &nbsp; &nbsp;</p><h2><b>DIVISION:</b></h2>EPD Established Pharma<p style="text-align:inherit">&nbsp; &nbsp; &nbsp; &nbsp;&nbsp;</p><h2><b>LOCATION:</b></h2>Thailand &gt; Bangkok : Q-House Lumpini Building<p style="text-align:inherit">&nbsp; &nbsp; &nbsp;</p><h2><b>ADDITIONAL LOCATIONS:</b></h2><p style="text-align:inherit">&nbsp; &nbsp; &nbsp;</p><h2><b>WORK SHIFT:</b></h2>Standard<p style="text-align:inherit">&nbsp; &nbsp; &nbsp;</p><h2><b>TRAVEL:</b></h2>Yes, 15 % of the Time<p style="text-align:inherit">&nbsp; &nbsp; &nbsp;</p><h2><b>MEDICAL SURVEILLANCE:</b></h2>Yes<p style="text-align:inherit">&nbsp; &nbsp; &nbsp;</p><h2><b>SIGNIFICANT WORK ACTIVITIES:</b></h2>Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)<p style="text-align:inherit">&nbsp; &nbsp; &nbsp;</p><p style="text-align:inherit">     </p><p style="text-align:inherit">     </p>