Regional Medical Scientific Director – Myeloid

This is a fully remote position, open to applicants in Connecticut, +4 more states.

📋 Description

• Engage in two-way scientific and medical information exchange with Scientific Leaders.

• Offer balanced and factual scientific information regarding non-product areas and address scientific inquiries, including those concerning Company products.

• Build and maintain professional relationships with both national and regional Scientific Leaders.

• Facilitate peer-to-peer scientific discussions while ensuring consistent medical contact with Scientific Leaders.

• Address scientific inquiries and refer out-of-scope questions to the relevant Company resources.

• Keep up-to-date with the evolving scientific and clinical landscape in the pertinent therapeutic area.

• Initiate conversations with Scientific Leaders and potential investigators about scientific/data exchange, research methodologies, study concepts, scientific validity, and qualifications.

• Improve understanding of investigator-sponsored research foundations and objectives.

• Identify challenges related to patient enrollment and retention.

• Suggest study sites and pinpoint potential investigators for Phase II-IV clinical development programs.

• Conduct Site Initiation Visits and assist protocol leadership in Global Clinical Trial Operations.

• Respond to investigator inquiries and provide information regarding Company-sponsored clinical studies.

• Participate in scientific congresses and medical meetings, facilitating scientific/data exchange for both Company and competitor data.

• Collect feedback and insights on the medical or scientific needs, priorities, and concerns of Scientific Leaders and patients.

• Act as a role model and assist in onboarding and sharing therapeutic expertise.

• Foster an inclusive environment that promotes belonging and empowerment.

⛳️ Requirements

• PhD, PharmD, DNP, DO, or MD required.

• At least 3 years of relevant therapeutic area experience beyond the terminal degree program.

• Capability to engage in doctoral-level discussions with key external stakeholders.

• Commitment to scientific excellence with a strong emphasis on scientific education and dialogue.

• Exceptional stakeholder management, communication, and networking abilities.

• Comprehensive understanding of FDA, OIG, HIPAA, and other ethical guidelines, laws, and regulations pertinent to the pharmaceutical sector and its clientele.

• Skill in organizing, prioritizing, and working efficiently in a fast-paced and changing environment.

• Proficient knowledge of Microsoft Office Suite (Word, PowerPoint, Excel, Teams, OneNote).

• Familiarity with virtual meeting platforms.

• Consistent compliance with field and corporate policies, Global Medical Scientific Affairs strategy, field SOPs, GCP guidelines, and administrative/operational duties.

• Required expertise in malignant hematology, medical affairs, medical knowledge, oncology, pharmaceutical medical affairs, professional networking, scientific communications, scientific research, and stakeholder engagement.

• Possession of a current valid driving license.

• Willingness and ability to travel 50% of the time.

• Must reside in the United States or Puerto Rico.

• No visa sponsorship available.

🏝️ Benefits

• Annual bonus.

• Long-term incentive, if applicable.

• Healthcare coverage including medical, dental, and vision.

• Additional insurance benefits for employees and their families.

• Retirement benefits, including a 401(k) plan.

• Paid holidays.

• Vacation time.

• Compassionate leave.

• Sick leave.

• Remote work options.

• No relocation assistance available.