Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

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.
Syneos Health

Medical Strategist – Oncology

Syneos Health

. Deliver medical and scientific contributions across clinical development programs and strategic partnerships .

Posted 11/5/2026full-timeMorrisville • North Carolina • United StatesSeniorLead💰 $142,300 - $256,100 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical trial design, protocol development, and regulatory compliance, with a strong focus on therapeutic strategy and client relationship management. Proven ability to translate scientific strategy into actionable clinical plans while collaborating effectively with multidisciplinary teams.

Highest-signal resume keywords
Medical Degree (MD, DO, or Equivalent)Clinical Trial DesignICH-GCP GuidelinesTherapeutic Strategy DevelopmentClient Relationship Management

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Protocol DevelopmentMedical ReviewRegulatory ComplianceFeasibility AssessmentsRisk Mitigation StrategiesBid DefenseStudy DesignTherapeutic InsightDecentralized TrialsAdaptive Design
Soft Skills
CollaborationNegotiationCommunicationStrategic ThinkingRelationship Building
Certifications & Qualifications
PhDMPHMBA
Industry Keywords
Clinical DevelopmentCROBusiness DevelopmentOperational FeasibilityScientific RigorClient SolutionsMedical Monitoring PlansDigital BiomarkersOncologyRegulatory Affairs

About the role

Key responsibilities & impact
  • Deliver medical and scientific contributions across clinical development programs and strategic partnerships
  • Ensure medical integrity, scientific rigor, and strategic alignment of proposals, protocols, and development plans
  • Translate scientific strategy into actionable clinical plans, including protocol development, indication positioning, and feasibility assessments
  • Support business development through RFP responses, bid defenses, and client solutions
  • Serve as medical lead in multidisciplinary teams responding to RFPs
  • Contribute to study design, indication strategy, and operational feasibility assessments
  • Provide therapeutic and medical insight during bid defense meetings and client consultations
  • Collaborate with business development and operational teams to align proposed solutions with client goals, budgets, and timelines
  • Maintain awareness of and share insights on industry pipeline and the scientific and business landscape
  • Lead development of clinical trial protocols, medical monitoring plans, and other key deliverables
  • Ensure scientific accuracy and regulatory compliance of medical content and clinical strategies
  • Provide expert input into therapeutic feasibility analyses, indication assessments, and risk mitigation strategies
  • Act as a key contact for medical and strategic questions throughout the proposal and trial lifecycle
  • Build client relationships as a trusted advisor and ensure high-quality service delivery
  • Collaborate with Clinical Operations, Regulatory Affairs, Biostatistics, and Pharmacovigilance teams
  • Provide subject matter expertise in at least one therapeutic area, including Oncology
  • Stay abreast of medical and regulatory developments affecting clinical trial design and execution
  • Champion innovative technologies and methodologies such as decentralized trials, adaptive design, and digital biomarkers
  • Contribute to white papers, conference presentations, and publications representing the CRO’s thought leadership

Requirements

What you’ll need
  • Medical degree (MD, DO, or equivalent)
  • Additional training such as PhD, MPH, or MBA is advantageous
  • 8-10 years of relevant experience for Senior or 10–15 years for Executive
  • At least 5 years in a CRO or client-facing strategic role
  • Strong knowledge of ICH-GCP guidelines, clinical trial design, and global regulatory requirements
  • Demonstrated experience in therapeutic strategy, protocol development, and medical review
  • Proven ability to collaborate with business development teams and present to clients
  • Ability to simplify complex scientific information for diverse audiences
  • Ability to understand customer needs, have difficult conversations, negotiate solutions, and understand impacts on the overall offering
  • Advanced business acumen, innovative and strategic thinking, confidence with financial considerations, negotiation and influencing skills, and comfort in sales and operational environments
  • Ability to establish and maintain effective relationships with internal and external stakeholders
  • Fluency in written and spoken English
  • Travel up to 60% may be required

Benefits

Comp & perks
  • Career development and progression
  • Supportive and engaged line management
  • Technical and therapeutic area training
  • Peer recognition and total rewards program
  • Company car or car allowance
  • Medical, Dental and Vision health benefits
  • Company match 401k
  • Eligibility to earn commissions/bonus based on company and individual performance
  • Flexible paid time off (PTO)
  • Sick time
  • Reasonable accommodations when appropriate