Senior Medical Affairs Manager Pharma
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Job Location:
Monthly Salary:
Posted on:
8 hours ago
Vacancies:
1 Vacancy
Job Summary
JOB DESCRIPTION:
PRIMARY OBJECTIVE:
The position represents the affiliates 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.
CORE JOB RESPONSIBILITIES:
- Develop and maintain in depth knowledge for assigned product(s)/ relevant therapeutic area(s)
- Provide expert medical/scientific advice for assigned products and related therapeutic areas
- Provide medical/scientific input into marketing strategy and key commercial initiatives as required. Deliver scientific and medical education programs to healthcare professionals
- 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
- Develop scientific material and initiates its request for approval
- 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
- Assures that clinical research program design meets scientific objectives and is aligned with our Medical Affairs Strategy
- Ensure compliance with Corporate and Divisional Standard Operating Procedures SOPs Good Clinical Practice and local regulatory requirements pertaining to the conduct of clinical studies
- Building relationships with Investigators and applying their inputs to enhance study design and protocols
- Provide monitoring visits and site management for a variety of protocols sites and therapeutic areas
- Collaborate and liaise with study team members for project execution support as appropriate
- Serves as scientific expertise on clinical research matters and govern regulatory requirements
- Administer and maintain appropriate documentation such as protocol approval and related study expenditure to internal stakeholders
- Accountable for supporting sites to adapt drive and track subject recruitment plan in line with project needs to enhance predictability
- Manage internal TARC review and approval of local clinical activities in assigned therapeutic area(s)
- Lead local clinical trial application through central research committee (if required)
- Complete data entry to monthly metric
- Manage CLIMATE and Clinical Tracker Sharepoint
- 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
EDUCATION/QUALIFICATIONS/EXPERIENCE:
- Bachelors degree in a pharmacy plus a higher education in a masters degree.
- Minimum 2 years Medical Affairs Manager experience in pharmaceutical company
- Excellent ability to prioritize and handle multiple tasks
- Good project management analytical decision-making
- General knowledge on drug development and clinical research an advantage
- Keen interest in developing and maintaining expert knowledge for assigned therapeutic area/product and in medical research in general
- Excellent communication skills including strong presentation skills
- High customer orientation
- Excellent skills to set stakeholders relationship networking tact and diplomacy
- Fluent in English and Thai (both verbal and written)
- Good computer skills and ability to learn and to adapt working with IT systems
- Knowledge of ICH GCP regulations industry practices and applicable standards
- Strong commitment to compliance with the relevant rules and procedures and to scientific quality and integrity
- Willingness to travel upcountry and oversea
The base pay for this position is
N/AIn specific locations the pay range may vary from the range posted.
JOB FAMILY:
Medical & Scientific Affairs
DIVISION:
EPD Established Pharma
LOCATION:
Thailand > Bangkok : Q-House Lumpini Building
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes 15 % of the Time
MEDICAL SURVEILLANCE:
Yes
SIGNIFICANT WORK ACTIVITIES:
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)
Required Experience:
Manager
Key Skills
- Proofreading
- Adobe Acrobat
- FDA Regulations
- Manufacturing & Controls
- Biotechnology
- Clinical Trials
- Research & Development
- GLP
- cGMP
- Product Development
- Chemistry
- Writing Skills
About Company
WHO WE ARE CREATING LIFE-CHANGING TECHNOLOGY From removing the regular pain of fingersticks as people manage their diabetes to connecting patients to doctors with real-time information monitoring their hearts, from easing chronic pain and movement disorders to testing half the world’s ... View more
