Board Certified Medical Affairs Specialist (BCMAS) Canada

Note: You will be directed to the BCMAS website to register directly through ACMA
In a new BenchSmart™ report entitled BENCHMARK STUDY ON MEDICAL AFFAIRS IN THE CANADIAN PHARMACEUTICAL INDUSTRY;
“Participants recommended offering Medical Affairs training and certification to those interested in developing the competencies necessary for a future career in MA.”
The ACMA Board Certified Medical Affairs Specialist Program (BCMAS) offers an in-depth perspective on the dynamic role medical affairs / MSLs plays in scientific exchange and data generation. This thought-provoking entirely online program encompasses the most comprehensive overview of the integral concepts necessary to be successful as a medical affairs professional / MSL in the pharmaceutical, biotechnology, and medical device industries. This program also includes important topics such as health economics outcomes research, regulatory affairs, clinical trial design, and presentation and communication skills.
The BCMAS program connects you to the clinical knowledge real-world experience, and leadership skills needed to be successful within the pharmaceutical industry’s clinical medical affairs / MSL space.
What Does the BCMAS Indicate?
- Improved professional stature & credibility
- Recognition as an advanced medical affairs professional
- Your commitment to continued professional development
- Thorough understanding of Pharma Industry ethics & compliance standards
PROGRAM OBJECTIVES
After completing the program, the participant will be able to:
- Develop critical and strategic thinking that is necessary to understand how medical affairs operates and integrates with other functions
- Acquire knowledge of medical affairs practices that are necessary to guide in the development, implementation, and evaluation of both data dissemination and presentation strategies: this will enhance HCP knowledge and ultimately improve patient care
- Develop the leadership and management skill necessary to facilitate socio-scientific and organizational change within your institution
- Enhance knowledge in both regulatory and compliance issues related to publications, clinical trials, drug development, and interactions with health care providers
WHO CAN TAKE THE COURSE?
The program is recommended for: medical affairs professionals/MSLs and clinical development/clinical operations professionals and those who aspire to these positions.
ELIGIBILITY REQUIREMENTS
- Current MSLs and MA personnel
- Non doctoral-degree with relevant industry experience
- Graduated with a PharmD, MD, DO, or PhD from an accredited program
EXAM INFORMATION
The BCMAS Certification Exam is a proctored, three-hour on-line exam administered online with ProctorU. The exam has three sections:
- Multiple choice questions
- Case studies
- True and False
What will I need for the exam:
- Calculator
- Pencil/Pen
- Web camera
EXAM SCHEDULING
The exam can be scheduled at any time that is convenient for the learner’s schedule through ProctorU.
NOTE
This course will count towards CCPE awards but is not eligible for CCPE medals
Course Features
- Suggested Hours of Study 20
- Quizzes 0
- Suggested Hours of Study 40 hours
- Course Completion 6 months
- Course Format E-Learning
- RxTx No
- Language English
- C.E. Credits What is this? 4
Exam Details
- Time Limit 3 hrs (see exam info)
- Passing Grade 70 %
Pricing
- Price $2600 CDN
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The Pharmaceutical Industry
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Medical Device Industry
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Diagnostics Industry
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Rules Governing Interactions with Healthcare Professionals
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Health Economics Outcome Research
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Evidence-Based Medicine
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Clinical Trial Designs
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Presentation and Communication Skills
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Regulatory Affairs
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Compliance
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Abstract and Medical Writing
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Publication Practices
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Drug Development Process
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Medical Information
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Medical Science Liaisons and Field Based Medical Teams
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Grant and Investigator-Initiated Study Funding and Process
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Advisory Boards
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Post-Approval Studies
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Risk Management Plans (RMP)
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Medication Safety and Pharmacovigilance