채용
Benefits & Perks
•Healthcare
•401(k)
•Healthcare
•401k
Required Skills
Medical affairs management
Clinical research
Scientific writing
Project management
Regulatory knowledge
GCP knowledge
JOB DESCRIPTION:PRIMARY OBJECTIVE:
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.
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:
- Bachelor’s degree in a pharmacy plus a higher education in a master’s 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)
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About Abbott

Abbott
PublicAbbott is a global healthcare company that develops medical devices, diagnostics, branded generic medicines, and nutrition products.
10,001+
Employees
Abbott Park
Headquarters
Reviews
3.4
10 reviews
Work Life Balance
2.5
Compensation
4.0
Culture
2.8
Career
3.2
Management
2.5
45%
Recommend to a Friend
Pros
Good benefits and compensation
Supportive management/teams
Good company reputation and mission
Cons
Poor management and communication
Stressful work environment
Limited career advancement/favoritism
Salary Ranges
1,330 data points
Mid/L4
Senior/L5
Intern
Mid/L4 · Project Manager
215 reports
$136,922
total / year
Base
$117,670
Stock
-
Bonus
$11,503
$94,554
$201,278
Interview Experience
3 interviews
Difficulty
2.7
/ 5
Duration
14-28 weeks
Offer Rate
67%
Experience
Positive 67%
Neutral 33%
Negative 0%
Interview Process
1
Application Review
2
Recruiter Screen
3
Phone Screen
4
Hiring Manager Interview
5
In-person/Final Interview
6
Offer
Common Questions
Technical Knowledge
Behavioral/STAR
Past Experience
Culture Fit
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