Eli Lilly and
Associate Director - Oncology - Clinical Laboratory Sciences
Eli Lilly and, Myrtle Point, Oregon, United States, 97458
Employer Industry: Pharmaceutical and Biotechnology
Salary up to $179,300
Eligibility for a company bonus based on performance
Comprehensive benefits package including medical, dental, vision, and 401(k) participation
Opportunities for career advancement and professional development within a leading global healthcare company
Supportive work environment with a commitment to diversity and inclusion
Chance to make a significant impact on oncology drug development and patient care
What to Expect (Job Responsibilities)
Collaborate with business and therapeutic teams to develop clinical lab, diagnostic, and biomarker strategies for trials and compounds
Shape protocol design for clinical laboratory operations and patient/site requirements
Execute clinical and biomarker sampling plans for clinical trials in coordination with Clinical Laboratory Sciences Associates
Maintain accurate inventory of research and clinical samples across drug programs and third-party labs
Participate in budget planning activities and provide integrated cost/time estimates for clinical trial lab plans
What is Required (Qualifications)
Bachelor’s degree with at least three years of experience in clinical drug development, preferably in oncology, focusing on laboratory sciences and diagnostics
Legal authorization to work in the United States; sponsorship for employment visa status is not provided
Demonstrated analytical, technological, and project management expertise
Proven ability to influence cross-functionally without direct authority
Experience in clinical diagnostic and laboratory needs in oncology in a regulated setting
How to Stand Out (Preferred Qualifications)
Advanced degree (e.g., MSc, PhD) in a scientific or healthcare field
Companion Dx development experience and sample management
Demonstrated ability to set and implement strategies to improve complex oncology drug development processes
Proven ability to lead the development of innovative clinical laboratory solutions
Experience developing diverse organizational talent with potential for growth
#Pharmaceutical #Oncology #ClinicalDevelopment #CareerOpportunity #DiversityAndInclusion
We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. If you encounter any employer not adhering to these principles, please bring it to our attention immediately.
We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer.
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Salary up to $179,300
Eligibility for a company bonus based on performance
Comprehensive benefits package including medical, dental, vision, and 401(k) participation
Opportunities for career advancement and professional development within a leading global healthcare company
Supportive work environment with a commitment to diversity and inclusion
Chance to make a significant impact on oncology drug development and patient care
What to Expect (Job Responsibilities)
Collaborate with business and therapeutic teams to develop clinical lab, diagnostic, and biomarker strategies for trials and compounds
Shape protocol design for clinical laboratory operations and patient/site requirements
Execute clinical and biomarker sampling plans for clinical trials in coordination with Clinical Laboratory Sciences Associates
Maintain accurate inventory of research and clinical samples across drug programs and third-party labs
Participate in budget planning activities and provide integrated cost/time estimates for clinical trial lab plans
What is Required (Qualifications)
Bachelor’s degree with at least three years of experience in clinical drug development, preferably in oncology, focusing on laboratory sciences and diagnostics
Legal authorization to work in the United States; sponsorship for employment visa status is not provided
Demonstrated analytical, technological, and project management expertise
Proven ability to influence cross-functionally without direct authority
Experience in clinical diagnostic and laboratory needs in oncology in a regulated setting
How to Stand Out (Preferred Qualifications)
Advanced degree (e.g., MSc, PhD) in a scientific or healthcare field
Companion Dx development experience and sample management
Demonstrated ability to set and implement strategies to improve complex oncology drug development processes
Proven ability to lead the development of innovative clinical laboratory solutions
Experience developing diverse organizational talent with potential for growth
#Pharmaceutical #Oncology #ClinicalDevelopment #CareerOpportunity #DiversityAndInclusion
We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. If you encounter any employer not adhering to these principles, please bring it to our attention immediately.
We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer.
#J-18808-Ljbffr