- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. **Purpose:** The Trial Capabilities Associate (TCA) provides clinical trial ... maintenance and close-out. The TCA may be assigned responsibilities within any trial capability, including obtaining clinical trial authorizations and ethics… more
- Lilly (Indianapolis, IN)
- …that will help solve our world's greatest health challenges. North America Trial Capabilities supports clinical development, a critical component to Lilly's ... Associate Director provides leadership, guidance and technical expertise to the Trial Capabilities Consultants, Associates and Assistants focusing on results… more
- Ankura (Atlanta, GA)
- …Lateral Thinking That Deliversᵀᴹ, hard-earned experience, expertise, and multidisciplinary capabilities drive results and Ankura is unrivalled in its ability ... to assist clients to Protect, Create, and Recover Valueᵀᴹ. For more information, please visit, ankura.com. more
- Bristol Myers Squibb (Princeton, NJ)
- …+ Develop and communicate a product vision, strategy, and roadmap for Trial Simulation & Modeling that align with business objectives and market opportunities. ... data products, and analytic ready data solutions for GDD Clinical Intelligence ( Trial Simulation & Modeling, Clinical Data Review, Programming and Submission). +… more
- Lilly (Indianapolis, IN)
- …3 days onsite/2 days remote **Purpose:** This role is responsible for trial level clinical data strategy including database structure, content and meaning, ... and deliver clinical data management packages. This role is responsible for providing trial leadership and ownership for a particular trial , set of trials,… more
- AbbVie (Oregon City, OR)
- …research, turning science into medicine for patients, and leveraging advanced capabilities to drive industry-leading performance. The CRA II partners with ... trials. The role focuses on site clinical research by ensuring proper trial conduct, while continually working to improve data integrity, compliance, overall study… more
- Gilead Sciences, Inc. (Foster City, CA)
- …timely and high-quality clinical data that supports clinical study endpoints. ** Associate Director, Biomarker and Bioanalytical Operations** leads a team of direct ... and bioanalytical strategy in clinical trials + Strong knowledge of clinical trial processes, thorough knowledge of sample management, and regulatory requirements. +… more
- AbbVie (Waltham, MA)
- …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director, Patient Centered Outcomes Research, is responsible for the ... functions (eg, Clinical Development & Operations, Regulatory, Commercial). The Associate Director, Patient-Centered Outcomes Research, will support multiple programs… more
- Merck (North Wales, PA)
- …spanning all our company therapeutic areas except early oncology. The Associate Principal Programmer will gather and interpret user requirements for analysis ... develop tables and figures according to statistical/modeling analysis plan. The Associate Principal Programmer will partner with stakeholders to solve problems;… more
- Merck (Rahway, NJ)
- …or related field plus 9 years SAS programming experience in a clinical trial environment. + MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, ... plus 7 or more years SAS programming experience in a clinical trial environment. **Department Required Skills and Experience:** + Excellent interpersonal skills and… more