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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in oncology clinical research and the execution of clinical trials, with a strong ability to translate scientific insights into strategic recommendations. Proven track record in building collaborative relationships with stakeholders and maintaining compliance with regulatory standards.
Highest-signal resume keywords
Oncology Clinical ResearchClinical Trials ExecutionScientific CommunicationStakeholder EngagementRegulatory Compliance
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Advanced Degree in Scientific DisciplineMedical Affairs ExperienceScientific Methods ApplicationClinical Development KnowledgeProblem-Solving Skills
Soft Skills
Excellent InitiativeJudgmentRelationship BuildingCommunication SkillsCollaboration
Industry Keywords
Clinical ResearchPharmaceutical IndustryMedical StrategyField Medical InsightsCompliance Standards
About the role
Key responsibilities & impact- Facilitate clinical research and interventional phase 1–3 trials with AbbVie drugs
- Support requests for medical and scientific information on products and therapeutic areas
- Partner with Site Management & Monitoring staff on site feasibility, site engagement, training, recruitment issues and site queries
- Provide senior scientific input into study feasibility, site identification and selection, recruitment strategy and medically complex site questions
- Build and maintain relationships with investigators, thought leaders, scientific institutions and collaborative study groups
- Consult with physicians, pharmacists and other medical professionals regarding patient referral to clinical trial sites and clinical practice topics
- Facilitate investigator-initiated study ideas and pipeline collaboration requests
- Deliver scientific presentations on the disease area and AbbVie’s pipeline
- Identify qualified external experts for research collaborations, advisory boards, congresses and symposia
- Identify R&D collaboration opportunities and liaise with Search & Evaluation, Discovery and Clinical Development teams
- Generate and communicate medical and scientific field intelligence
- Provide strategic scientific input to protocol feasibility, country and site strategy, evidence needs and development decisions
- Attend relevant internal and external scientific meetings and conferences
- Assist with named-patient or compassionate-use requests when requested
- Provide early-touchpoint insights on clinical practice, external experts and future clinical development programs
- Develop long-term medical strategy and plans from clinical trials through health authority approval and access
- Provide senior scientific leadership across affiliate, regional and global interfaces and translate field insights into actionable recommendations
- Ensure all activities comply with applicable laws, regulations, guidelines, codes of conduct and AbbVie policies
- Provide scientific and technical input to local study teams, brand teams and external investigators
- Develop collaborative relationships that facilitate AbbVie research and contribute to pipeline success
- Potentially provide scientific coaching and best-practice guidance to Pipeline MSLs and other field medical colleagues
Requirements
What you’ll need- Advanced degree (e.g. PhD, PharmD, etc.) in a relevant scientific and biologic discipline is strongly preferred; candidates with an undergraduate degree in a relevant discipline and demonstrated experience will be considered
- At least 8+ years of professional experience in medical affairs or a similar field-based R&D role involving clinical trials and clinical development
- Strong understanding of the oncology clinical research landscape and implementation and conduct of oncology clinical trials
- Ability to connect clinical-trial execution, external scientific insights and the evolving competitive landscape with portfolio-level medical and development priorities
- Demonstrated ability to develop and maintain excellent working relationships with internal stakeholders, study investigators and site staff
- Solid knowledge and problem-solving skills to advance the medical and scientific objectives of a pharmaceutical company
- Ability to translate complex scientific, clinical and field information into strategic recommendations influencing cross-functional and senior stakeholders
- Excellent initiative and judgment and ability to represent AbbVie in a compliant manner
- Expertise in scientific methods applied to clinical research and current legislative/regulatory controls applicable to this research
- Excellent written and spoken communication and presentation skills
- Ability to develop and maintain strong collaborative relationships with thought leaders, physicians and other healthcare decision makers
- Ability to engage effectively in both Korean and English with affiliate, regional and global stakeholders
- Good understanding of written and oral English is desirable
- Strong commitment to compliance with relevant rules and procedures and to scientific quality and integrity
Benefits
Comp & perks- Equal opportunity employer
- Commitment to operating with integrity, driving innovation, transforming lives and serving the community