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.
Senior Clinical Development Scientist
Gilead Sciences. Support late-stage oncology clinical development .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in late-stage oncology clinical development, including protocol preparation, regulatory compliance, and data analysis. Proven ability to lead teams, adapt to changing project needs, and communicate effectively within clinical research environments.
Highest-signal resume keywords
PharmD Or PhD In Clinical ResearchMultiple Myeloma ExperienceCAR-T Therapy ExperienceFDA And EMA Regulations KnowledgeGood Clinical Practice (GCP) Standards
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Study Start-UpData AnalysisProtocol DevelopmentRegulatory Filings SupportClinical MonitoringData Management ManualsCRFs ContributionScientific PresentationsStudy Concept SheetsInvestigator Meeting Notebooks
Soft Skills
Strong Communication SkillsOrganizational SkillsAnalytical AbilitiesFlexibility And AdaptabilityTeam Coordination
Tools & Technologies
Microsoft Office
Industry Keywords
Oncology Clinical DevelopmentDrug Development PhasesICH GuidelinesClinical TrialsGilead SOPs
About the role
Key responsibilities & impact- Support late-stage oncology clinical development
- Collaborate with the Clinical Scientist Program Lead on ongoing clinical trial program activities
- Collaborate on functional area activities during program implementation
- Support clinical study start-up, execution, and closeout
- Contribute to data analysis and reporting
- Support regulatory filings
- Develop study concept sheets and protocols
- Participate in protocol review discussions
- Prepare protocols, amendments, study manual sections, Investigator meeting notebooks, and related documents
- Contribute to CRFs, Data Management Manuals, and Data Analysis Plans
- Address scientific and procedural questions from Investigators
- Contribute to data listings, summary tables, study results, manuscripts, and scientific presentations
- Assist with regulatory documents
- Anticipate obstacles and implement solutions with guidance
- Coordinate teams and provide direction when requested
- Provide clinical monitoring for clinical studies or study components
- Summarize published scientific information for new study development
- Adhere to regulatory requirements, Good Clinical Practice standards, and Gilead SOPs
- Create inclusion, develop talent, and empower teams as a people leader
Requirements
What you’ll need- PharmD or PhD in clinical research or clinical pharmacology with scientific and/or drug development experience
- MS with 6+ years’ relevant scientific and/or drug development experience
- BS or RN with 8+ years’ relevant scientific and/or drug development experience
- Relevant experience in Multiple Myeloma and/or CAR-T Therapy is preferred
- Experience with Microsoft Office and other job-related programs
- Ability to be a fast learner
- Ability to be flexible and adaptable to change and move between projects
- Proven analytical abilities through past experience and/or academic research
- Understanding of drug development phases and associated clinical trials
- Knowledge of FDA and EMA regulations, ICH guidelines, GCP and standard clinical procedures
- Strong communication and organizational skills
- Ability to travel when needed
Benefits
Comp & perks- Discretionary annual bonus
- Discretionary stock-based long-term incentives
- Paid time off
- Company-sponsored medical insurance
- Company-sponsored dental insurance
- Company-sponsored vision insurance
- Company-sponsored life insurance