- Merus (Cambridge, MA)
- Clinical Trial Associate /Senior Clinical Trial Associate Department: Clinical Operations Employment Type: Full Time Location: Cambridge, MA Description ... The Clinical Trial Assistant (CTA) / Senior CTA plays a vital...standards. The CTA/Sr. CTA is responsible for maintaining essential trial documents, structuring filing systems, managing clinical systems, coordinating… more
- Dyne Therapeutics (Waltham, MA)
- …and follow us on X, LinkedIn and Facebook. Role Summary: The Clinical Trial Associate (CTA) provides Clinical Operations support in the initiation, execution ... for proactive, study-wide problem solving regarding study progress and trial issues during the study Track metrics related to...as internal meetings Collect and track documents for the trial master file (TMF), and perform TMF reviews to… more
- Genmab (NJ)
- …like a fit? Then we would love to have you join us!The RoleThe Associate Director acts as a statistical expert supporting the clinical development of compounds as ... and/or indication lead for both early and late-stage programs, and/or as trial responsible statistician with responsibilities as described below. The Associate … more
- Vanguard-IP (Los Angeles, CA)
- …patent law and patent litigation practices. REQUIREMENTS Seeking a patent litigation associate with experience in trial , motions, depositions, expert reports, ... and discovery management. Additional requirements include strong organizational and writing skills, strong academic credentials including an undergraduate science degree, and a desire to excel in a law firm environment. SUMMARY Vanguard Intellectual Partners… more
- Merck & Co. (South San Francisco, CA)
- …West Point, PA / Rahway, NJ is seeking a curious and collaborative Associate Director to support our rapidly expanding cardiometabolic and ophthalmology pipelines. - ... As an Associate Director, you will represent QP2 on cr o...strategies ( translational PK/PD strategies, mechanistic model, POPPK/PD, clinical trial simulations, etc) for quantitative analyses, within and across… more
- Merck & Co. (North Wales, PA)
- …field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering ... plus 7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and Experience: Excellent interpersonal skills and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …rare diseases and immune disorders. Summary: Oversees typically a single non-pivotal trial (small size, standard complexity in design and geographic scope). Prepares ... guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to Clinical Operations. Represents… more
- Merck & Co. (North Wales, PA)
- …for the operational planning, feasibility, execution and conduct of clinical trial (s).Serves as the Clinical Trial Team lead. Leads and ... subsidiary country teams, vendors, committees, etc.) in support of clinical trial objectives.Liaises with partners, vendors, and vendor management team . Review… more
- Merck & Co. (San Francisco, CA)
- …of decision-making at our Company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. - This Associate ... PK/PD models, exposure response (ER) models, model-based meta-analysis (MBMA), clinical trial simulations (CTS) and disease progression modeling into programs and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …analyses and collection, missing data, demographic/representativeness of samples from clinical trial and screen failures.Clinical trial protocol development and ... reviews (clinical trial protocols and medical device protocols)ICF reviews to ensure adequate disclosure for collection, retention, testing and retesting of samplesProject Team Participation: Provide device-specific regulatory insight/guidance during CDx… more
- Merck & Co. (North Wales, PA)
- …field plus at least 7 years SAS programming experience in a clinical trial environment OR a Bachelor's degree in Computer Science, Statistics, Applied Mathematics, ... or related field plus 9 years SAS programming experience in a clinical trial environment. Required Skills and Experience: Experience in CDISC SDTM and ADaM standards… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and life-cycle ... Clinical Investigations, Clinical Judgment, Clinical Reporting, Clinical Research, Clinical Trial Documentation, Clinical Trial Planning, Consultative Approach,… more
- Insmed Incorporated (Los Angeles, CA)
- …Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Associate Director Medical Science Liaison will develop and maintain professional ... Clinical Operations, and Medical Affairs Departments. This may include trial site identification, ongoing recruitment motivation, and issue/problem solving.Provide… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …detection and characterization for ongoing studies and compound level pooled clinical trial data of project(s). Act as statistical expert consultant within company ... direction from group head and provide statistical scientific leadership for clinical trial safety data. Lead the statistical support for safety signal monitoring for… more
- Merck & Co. (San Francisco, CA)
- Job Description Position Description: Associate Director, DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) ... Under the broad guidance of the DSCS Digital Program Mgmt Lead, the Associate Director, DSCS Digital Project Manager, will be responsible for implementing improved… more
- Eisai, Inc (Nutley, NJ)
- …difference. If this is your profile, we want to hear from you. The Associate Director (AD), Global Medical Affairs Training and Education is responsible for the ... training (eg medical insights workshops, presentation skills, understanding clinical trial design, statistics, etc.) to supplement MSL development.Collaborate with… more
- Merck & Co. (Rahway, NJ)
- …and increasing overall operational effectiveness.We are seeking a dynamic and experienced Associate Director of Outside Counsel and Vendor Management to join our ... Report Automation, Supplier Management, Team Leadership, Training and Development, Trial Preparation, Vendor Contract Negotiations, Vendor Management, Vendor Management… more
- Infinium Staffing (Irvine, CA)
- Overview: The Litigation Associate Attorney performs substantive billable legal work under the supervision of the Managing Partner. This role supports the firm's ... hearings, and engaging in settlement negotiations. We are seeking a Litigation Associate Attorney who is passionate about helping property owners and landlords… more
- Formation Bio (New York, NY)
- …to patients faster and more efficiently.About the PositionWe are seeking an Associate Director, Program Management to drive the execution of critical drug ... execution, ensuring the team stays at the forefront of innovation in clinical trial operations. About You You're excited about the intersection of AI and program… more
- BUCHALTER, A PROFESSIONAL CORPORATION (Scottsdale, AZ)
- …AZ Education Level JD Description We are currently seeking a mid level associate to support our Scottsdale office's Litigation Practice Group. The ideal candidate ... case or first chair a simpler case Effectively assist lead trial attorneys in all pre- trial issues and proceedings Prepare complex pre- trial motions Assist… more
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