FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in scientific and medical information exchange, with a strong focus on stakeholder management and communication. Possesses a thorough understanding of FDA regulations and clinical development processes, alongside the ability to foster professional relationships within the therapeutic area.
Highest-signal resume keywords
PhD, PharmD, DNP, DO, Or MD3 Years Therapeutic Area ExperienceStakeholder ManagementFDA, OIG, HIPAA ComplianceMicrosoft Office Suite Proficiency
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Scientific Information ExchangeClinical Development ProgramsSite Initiation VisitsResearch StrategiesData ExchangeScientific DiscussionsPatient Enrollment StrategiesScientific PublicationGCP GuidelinesTherapeutic Area Knowledge
Soft Skills
Communication SkillsNetworking SkillsOrganizational SkillsDedication to Scientific ExcellenceTeam Collaboration
Tools & Technologies
Microsoft Office SuiteVirtual Meeting Platforms
Industry Keywords
GYN OncologyClinical Trial OperationsEthical GuidelinesField-Based Medical ExperienceInvestigator-Sponsored Research
About the role
Key responsibilities & impact- Engage in bidirectional scientific and medical information exchange with Scientific Leaders
- Provide balanced, factual scientific information on non-product areas and respond to scientific questions, including questions about Company products
- Develop professional relationships with national and regional Scientific Leaders
- Conduct peer-to-peer scientific discussions and maintain a reliable presence as a company medical contact
- Address scientific questions and direct out-of-scope inquiries to appropriate company resources
- Maintain current knowledge of the scientific and clinical environment in the relevant therapeutic area
- Initiate discussions with Scientific Leaders and potential investigators regarding scientific/data exchange, research strategies, study concepts, scientific merit, and qualifications
- Enhance understanding of investigator-sponsored research foundations and goals
- Identify barriers to patient enrollment and retention
- Recommend study sites and identify potential investigators for Phase II-IV clinical development programs
- Conduct Site Initiation Visits and support protocol leadership with Global Clinical Trial Operations
- Address investigator questions and provide information about Company-sponsored clinical studies
- Engage in scientific congresses and medical meetings and facilitate scientific and data exchange
- Gather feedback and insights on medical or scientific needs, priorities, and concerns of Scientific Leaders and patients
- Serve as a role model and support onboarding and sharing of therapeutic expertise
- Contribute to an inclusive environment and help create, lead, and retain the workforce
Requirements
What you’ll need- Minimum PhD, PharmD, DNP, DO, or MD
- Minimum 3 years of relevant therapeutic area experience beyond that obtained in the terminal degree program
- Ability to conduct doctoral-level discussions with key external stakeholders
- Dedication to scientific excellence with a strong focus on scientific education and dialogue
- Excellent stakeholder management, communication, and networking skills
- Thorough comprehension of FDA, OIG, HIPAA, and other relevant ethical guidelines, laws, and regulations
- Ability to organize, prioritize, and work effectively in a constantly changing environment
- Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel, Teams, OneNote)
- Familiarity with virtual meeting platforms
- Desire to contribute to an environment of belonging and empowerment
- Consistent adherence to field and corporate policies, GMSA strategy, field SOPs, GCP guidelines, and administrative/operational responsibilities
- Candidates must reside within the territory covering GA, FL, SC, AL, MS, and LA
- Ability to travel up to 50% within the territory
- Valid driving license required
- VISA sponsorship unavailable
- Preferred: field-based medical experience, with GYN Oncology strongly preferred
- Preferred: research experience
- Preferred: demonstrated record of scientific/medical publication
Benefits
Comp & perks- Annual bonus
- Long-term incentive, if applicable
- Medical, dental, and vision healthcare
- Other insurance benefits for employee and family
- Retirement benefits, including 401(k)
- Paid holidays
- Vacation
- Compassionate days
- Sick days
- Remote work arrangement