Director – Clinical Research Scientist – Immunology/Gastroenterology Development
Eli Lilly and Company
full-time
Posted on:
Location Type: Remote
Location: United States
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Salary
💰 $177,000 - $338,800 per year
Job Level
About the role
- The primary responsibilities of the Development CRS are generally related to late-phase and marketed compounds.
- Clinical Planning: product lifecycle plan, clinical strategies, development plans and study protocol design.
- Provide subject matter expertise and keep updated with the pre-clinical and clinical data relevant to the molecule.
- Clinical Trial Execution and Support: Plans, collaborates on and reviews scientific content of clinical documents such as protocols, informed consent documents, final study reports, and submissions.
- Supports the monitoring of patient safety during study and engages in the global product safety reviews.
- Cross function collaboration with clinical trial teams in the design, conduct and reporting of mid to late phase clinical trials.
- Conduct study start-up meetings, investigator meetings and other activities to provide the appropriate training and information to investigators and site personnel.
- Engage in reporting of clinical trial data in Clinical Trial Registry activities.
- Support the planning of symposia, advisory board meetings, and other meetings with health care professionals.
- Establish and maintain collaborations and relationships with thought leaders.
- Support clinical trial data analysis and publications.
- Provide medical expertise to regulatory scientists and support regulatory strategy.
Requirements
- An advanced health/medical/scientific (for example, in Pharmacology, physiology, microbiology) or related graduate degree such as, PharmD, PhD
- 3+ years of clinical development experience, including mid-to-late-stage development
- Demonstrated ability to balance scientific priorities with business priorities with examples of successful leadership skills
- Demonstrated strong communication, interpersonal, teamwork, organizational, and negotiation skills
- Previous GI drug development experience
- Pediatric drug development experience
- Oral/written communication/listening skills are essential
- Strong relationship-building and interaction skills with peers and management
Benefits
- eligibility to participate in a company-sponsored 401(k)
- pension
- vacation benefits
- eligibility for medical, dental, vision and prescription drug benefits
- flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
- life insurance and death benefits
- certain time off and leave of absence benefits
- well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical planningclinical strategiesdevelopment plansstudy protocol designclinical trial executionclinical trial data analysisregulatory strategyclinical document reviewpatient safety monitoringGI drug development
Soft skills
leadershipcommunicationinterpersonal skillsteamworkorganizational skillsnegotiation skillsrelationship-buildinginteraction skillslistening skills
Certifications
PharmDPhD