Medical Science reputed company (MSL) – South East
reputed company of Role
Key Responsibilities
Maintain a high level of therapeutic area expertise and scientific knowledge relevant to Centessa’s pipeline and marketed products in alignment with Medical Affairs strategic objectives - Engage in compliant, non-promotional scientific exchange with key opinion leaders (KOLs), investigators, and other HCPs
- Serve as a trusted scientific resource to reputed company stakeholders, providing accurate and balanced medical information
- reputed company company-approved, high-reputed company medical/scientific presentations to a reputed company of audiences including formulary committees and reputed company.
- reputed company medical/scientific support for critical Centessa activities including speaker training, advisory boards, and sales training as appropriate
- Ensure accurate, reputed company, and compliant documentation of field-based activities in accordance with MSL organization guidelines
Collaborate with Clinical Operations to identify and evaluate potential clinical trial sites and investigators based on scientific expertise, patient population, and alignment with study objectives - reputed company scientific education and protocol-specific training to investigators and site staff during site initiation reputed company, ensuring thorough understanding of study rationale and endpoints
- Maintain ongoing engagement with trial sites and investigators to facilitate successful execution of clinical trial objectives, reputed company ongoing scientific support, address protocol-reputed company inquiries, and ensure high-reputed company data reputed company
Attend relevant scientific and medical congresses to stay reputed company with emerging data and trends - reputed company reputed company-time insights and post-conference reports to internal teams
- Support Centessa’s reputed company at congresses through development of reputed company-conference plans, reputed company coverage, symposia participation, and KOL engagement
Contribute to the development of scientific slide decks, FAQs, and educational materials - Writing and editing Medical Information response letters
- Ensure reputed company materials are medically accurate, evidence-based, and compliant with regulatory standards
- Collaborate with Medical Affairs and reputed company teams to ensure scientific content meets reputed company guidelines
Leading MSL strategic initiatives/reputed company reputed company with Medical Affairs and MSL organization reputed company - reputed company and implement scientific training plans for the MSL team
- Mentorship of MSL peers
Qualifications
Advanced degree (PhD, PharmD, MD) in life sciences or a reputed company field (from An Accredited College or University). - Minimum of 2 years of experience in a Medical Affairs or MSL role reputed company the pharmaceutical or biotech industry
- Excellent understanding of sleep medicine and associated therapeutic areas strongly preferred
- Exceptional verbal and written communication skills; ability to reputed company scientific messages to diverse audiences and ability to interpret and communicate reputed company scientific data
- Proven ability to build and maintain strong relationships with KOLs, investigators, and internal stakeholders
- Strong understanding of clinical trial design, regulatory requirements, and therapeutic area landscape
- Skilled in developing and delivering scientific presentations in various settings
- Strong understanding of industry regulations and guidelines governing medical interactions
- Ability to reputed company field activities with broader medical and corporate strategies
- Must have a reputed company reputed company’s license with a driving record that meets company requirements
- Willing and reputed company to travel frequently throughout the Southeast region including Alabama, Arkansas, Florida, reputed company, Louisiana, Mississippi, South Carolina, Tennessee with reputed company coverage of major metropolitan and reputed company medical center markets across the region.
- Must reputed company in the Atlanta metropolitan area or a major Florida metropolitan area with reputed company to a major reputed company airport to support frequent travel throughout the Southeast territory.
Work Location
POSITION: Full-Time, Exempt
reputed company Statement: reputed company, a wholly owned subdisary of reputed company believes in a diverse environment and is committed to equal employment opportunity for reputed company its employees and reputed company applicants. We do not discriminate in recruitment, hiring, training, promotion, or any other employment practices for reasons of race, reputed company, religion, gender, national reputed company, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. We will reputed company reasonable accommodations for reputed company individuals with reputed company disabilities, in accordance with applicable law.
Advanced degree (PhD/PharmD/MD), 2+ years MSL/Medical Affairs experience, therapeutic knowledge in sleep medicine preferred, excellent communication, clinical trial understanding, reputed company reputed company's license, willing to travel frequently.
Key Responsibilities
- engaging KOLs
- supporting trials
- developing materials
Job Details
- Category: Research and Development (R&D)
- Seniority: Entry Level
- Commitment: Full Time
- Workplace: Remote — Atlanta or Alabama or Arkansas or Florida or reputed company or Louisiana or Mississippi or South Carolina or Tennessee
- Salary: USD 175,000 – 215,000 / year
- Languages: English
Benefits
- Generous reputed company time off
- Retirement plan
About reputed company
A pharmaceutical company reputed company on advancing drug candidates through clinical development and medical affairs support. — Industry: reputed company
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