Doctorate level degree (Pharm.D., Ph.D., M.D., or D.O.), 5+ years of industry or related field experience, Extensive clinical or clinical trial experience in rare diseases and/or genetic medicine, Exceptional communication and presentation skills..
Key responsibilities:
Spearhead education of Principal Investigators and healthcare teams on CRISPR-based gene editing technologies
Foster strong relationships with investigators and institutional stakeholders
Develop and implement strategies to enhance patient recruitment and site activation
Gather and analyze insights on patient experiences and healthcare system dynamics.
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The Medical Affairs Company (TMAC)
51 - 200
Employees
About The Medical Affairs Company (TMAC)
Your Partners in Medical Affairs - The Medical Affairs Company (TMAC) provides a full range of flexible and customizable medical affairs solutions to meet our Clients' needs. TMAC’s services include the provision of contract field-based medical teams, medical information, and medical affairs consulting, all designed to address company resource, timing and budget challenges.
Field-based Medical Affairs Careers: We’ve set the industry standard in contract field-based medical affairs recruiting. TMAC’s internal specialized Talent Acquisition Team has a 20-year track record of success in building national field-based Medical Affairs and MSL Teams. They are adept at identifying and attracting the right individuals to fit the needs of each specific program and matching a candidate's talent to the skill set required for each position. Work alongside our clients, including many of the top ten pharma companies around the globe, as well as up and coming companies who are advancing cutting edge science and novel technology. Mesh your own science and business acumen as we improve the way medicine impacts lives. Whether you’re actively seeking a position or just keeping an open door to opportunities, we deliver the right people to the right companies, every time.
TMAC’s Executive Leaders and management team have been actively involved in the outsourced medical affairs sector for over 20 years and have continued to further develop and evolve strategic solutions that meet the needs of today’s biopharmaceutical, diagnostic and medical device clients. TMAC realizes that not all programs are alike and customizes each program to the specific company’s culture, therapeutic area, product lifecycle stage and stakeholders needs. The Management Team of department leads, field medical Directors & Managers is made up of some of the best talent in the industry with unmatched experience working with programs of all sizes and specialties and in a wide range of therapeutic areas.
Regional Scientific Director - Rare Disease, Gene Therapy (Southeast)
Be at the Forefront of Revolutionary Gene-Editing Therapies
The Medical Affairs Company (TMAC) is seeking visionary Regional Scientific Director (RSD) to join an expanding global field medical team. This is your opportunity to set the standard for a new class of medicine and make a lasting impact in the field of gene therapy.
About The Role
As a Regional Scientific Director, you will:
Spearhead the education of Principal Investigators, Centers of Excellence, Key Opinion Leaders, and healthcare teams on cutting-edge CRISPR-based gene editing technologies
Play a crucial role in our client's groundbreaking Phase 3 trials for Hereditary Angioedema and ATTR amyloidosis with cardiomyopathy
Bridge the gap between clinical development and real-world application of revolutionary therapies
Key Responsibilities
Foster strong relationships with investigators and institutional stakeholders to optimize clinical trial execution
Provide expert scientific support and operational insights to study sites
Develop and implement strategies to enhance patient recruitment and site activation
Educate stakeholders on CRISPR/Cas9 technology and emerging approaches in disease management
Gather and analyze valuable insights on patient experiences and healthcare system dynamics
Ideal Candidate Profile
Doctorate level degree (Pharm.D., Ph.D., M.D., or D.O.) with 5+ years of industry or related field experience
Extensive clinical or clinical trial experience in rare diseases and/or genetic medicine. Priority given to candidates with HAE experience.
Prior experience as a Medical Science Liaison or Clinical Trial Liaison
New product launch experience (preferred)
Exceptional communication and presentation skills
Strategic thinker with the ability to influence and drive results
Passion for advancing medical science and improving patient outcomes
What We Offer
Opportunity to work with cutting-edge gene-editing technologies
Collaborative and innovative work environment
Competitive salary commensurate with experience and expertise
Chance to make a significant impact on patient lives and the future of medicine
Are you ready to shape the future of medicine? Join us in revolutionizing healthcare through gene therapy. Apply now to be part of this exciting journey!
Note: This position requires 50-70% travel, including overnight stays. Candidates must have a valid driver's license and the ability to manage a geographically assigned territory from a home-based office.
Salary offers to be determined based on industry experience, education, and therapeutic expertise.
Required profile
Experience
Spoken language(s):
English
Check out the description to know which languages are mandatory.