- Lilly (Indianapolis, IN)
- …and geographic location. The anticipated wage for this position is $63,000 - $155,100 The Trial Capabilities Associate (TCA) provides clinical trial ... support of clinical development. The TCA is accountable for performing clinical trial site activation activities to ensure the investigator sites meet requirements… more
- Sumitomo Pharma (Columbus, OH)
- …. **Job Overview** The Sr. Clinical Trial Associate (CTA) is responsible ... diverse pipeline of early- to late-stage assets, and in-house advanced technology capabilities , we aim to accelerate discovery, research, and development to bring… more
- Ankura (GA)
- …producing large volumes of visuals in high-pressure environments. ROLE OVERVIEW: The Trial Technology Associate will be responsible for consulting with attorneys ... founded on innovation and growth. PRACTICE OVERVIEW: Ankura's Visual Communications & Trial Technology consulting group knows the power of visual persuasion. We… more
- Lilly (Branchburg, NJ)
- …for this position is $111,000 - $162,800 **Position Description:** The Clinical Trial (CT) Supply Management Associate Director will provide operational ... performance and speed drug development. **Responsibilities:** + Deliver improved clinical trial supply chain performance, assess and mitigate risk, and perform… 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
- Lilly (Indianapolis, IN)
- …(CDDA) provides leadership in the strategy and development of contemporary clinical trial processes, technologies, information, and capabilities and in shaping ... should have extensive experience supporting data collection and aggregation systems. Clinical Trial Foundations as part of Clinical Design, Delivery & Analytics… more
- Lilly (IN)
- …and other site staff. Lead internal relationships across the CDDA ( Trial Capabilities , Investigator Engagement, Patient Engagement, Clinical Design, Clinical ... (CCSI) organization is responsible for strategically planning and supplying materials, trial support services and innovative capabilities to support the… more
- Merck (North Wales, PA)
- **Job Description** **Position Description:** ** Associate Principal Statistical Programmer - Oncology (Hybrid)** In BARDS (Biostatistics and Research Decision ... programming analysis and reporting deliverables for global stakeholders. The Associate Principal Programmer will gather and interpret user requirements for… more
- AbbVie (Mettawa, IL)
- …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 (Rahway, NJ)
- …high-quality data to support decision making in clinical trials. The Associate Principal Scientist, Statistical Programmer supports the design, development, and ... plus 9 or more years of SAS programming experience in a clinical trial environment + MS in Computer Science, Statistics, Applied Mathematics, Life Sciences,… more
- Bristol Myers Squibb (Princeton, NJ)
- …and implementation of innovative strategies and technologies for clinical trial programming. Associate Director develop collaborative relationships and ... and in their personal lives. Read more: careers.bms.com/working-with-us . Associate Director, Statistical Programming, provides functional expertise and leadership… more
- Lilly (Indianapolis, IN)
- …Product, Commercial Product, and Ancillary strategies to ensure technology enables clinical trial design and execution. The Associate Director, Clinical Supply ... management of clinical processes, information, and technologies within Clinical Trial Foundations (CTF) organization, Clinical Supply and Delivery (CS&D)… more
- Takeda Pharmaceuticals (Boston, MA)
- …the development of scientific communications strategy and deliverables, the ** Associate Director, Scientific Communications Lead, Solid Tumors** proactively defines ... in life sciences, and excellent project management skills. The Associate Director, Scientific Communications Lead, develops and implements strategic publications… more
- BlackRock (Princeton, NJ)
- **About this role** ** Associate , Investment Accounting Migrations Specialist:** Are you an Investment Accounting professional searching for an exciting, significant, ... bringing strategic visions to fruition, then look no further! BlackRock is pursuing an Associate to become a part of the team. We recognize that strength comes from… more
- Sumitomo Pharma (Columbus, OH)
- …diverse pipeline of early- to late-stage assets, and in-house advanced technology capabilities , we aim to accelerate discovery, research, and development to bring ... a dynamic, highly motivated, and experienced individual for the position of Associate Director, elluminate (R) Data Programming. This role will drive the programming… more
- Merck (Rahway, NJ)
- …years Statistical Analysis System (SAS) programming experience in a clinical trial environment. + MS (preferred) in Computer Science, Statistics, Applied ... 7 years Statistical Analysis System (SAS) programming experience in a clinical trial environment. **Required Experience and Skills:** + Proven track record for… more
- Merck (Rahway, NJ)
- …in research activities for innovative statistical methods and applications in clinical trial development. + Mentors and guides junior staff in functional activities. ... eg SAS and/or R. + Good understanding of worldwide regulatory requirements and clinical trial expertise from phase II to V. + Strong oral and written communication… more
- Merck (Rahway, NJ)
- …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
- Gilead Sciences, Inc. (Foster City, CA)
- …and help create possible, together. **Job Description** Job Description ** Associate Director, Biostatistics** **Position Overview:** Are you passionate about ... our on-going regulatory submissions. If you have a solid background in clinical trial design and analysis and are eager to tackle challenges that drive scientific… more
- ADM (Kennesaw, GA)
- **92116BR** **Job Title:** Associate Director, Microbiome Regulatory Science - Kennesaw, GA **Department/Function:** Legal, Compliance, Regulatory Affairs, Corporate ... Security **Job Description:** ** Associate Director Microbiome - Decatur, IL; Chicago, IL: Erlanger,...and Wellness Clinical Trials Board (CTB), ensuring ADM's clinical trial strategy for is aligned with the RSA global… more