- Allen Spolden (New Brunswick, NJ)
- New Brunswick, United States | Posted on 12/14/2023 The remote‑based Clinical Trial Associate (CTA) will perform tasks related to supporting operational ... to support clinical study activities as defined by the clinical trial operating model. Perform developmental tasks with oversight of CTA Manager.… more
- Allen Spolden (New Brunswick, NJ)
- New Brunswick, United States | Posted on 12/14/2023 The remote-based Clinical Trial Associate (CTA) will perform tasks related to supporting operational ... to support clinical study activities as defined by the clinical trial operating model. Perform developmental tasks with oversight of CTA Manager.… more
- Allen Spolden (New Brunswick, NJ)
- A clinical research organization is seeking a Remote Clinical Trial Associate to support operational strategy and execute clinical studies. ... Responsibilities include assisting with study startup, ensuring regulatory readiness, and collaborating with study teams and CROs. Candidates should have a Bachelor's degree and at least one year of experience in the pharmaceutical industry, along with strong… more
- Allen Spolden (New Brunswick, NJ)
- A leading pharmaceutical company is seeking a Clinical Trial Associate (CTA) to support operational strategies in clinical studies. This remote position ... and have over 3 years of experience in the pharmaceutical industry or clinical research. The role necessitates some travel as needed. Generous benefits and time… more
- Regeneron Pharmaceuticals, Inc (Basking Ridge, NJ)
- …involved in research activities for innovative statistical methods and applications in clinical trial development as well as providing training to ... communication skills. Solid knowledge of statistical analysis methodologies, experimental and clinical trial design Expertise in statistical software Does this… more
- Shionogi Inc. in (Florham Park, NJ)
- …of audits, inspections, and quality investigations. Responsibilities Provide quality oversight of clinical trial operations and PV to ensure GCP and GVP ... Overview The Associate Director, GCP/GVP Quality Assurance provides senior-level quality...clinical study teams and advisory to PV. Evaluate clinical trial documentation, processes, and study plans… more
- Hispanic Alliance for Career Enhancement (Rahway, NJ)
- …Engineering or related field plus 9 years SAS programming experience in a clinical trial environment. MS in Computer Science, Statistics, Applied Mathematics, ... related field plus 7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and Experience: Excellent interpersonal… more
- The Association of Technology, Management and Applied… (Rahway, NJ)
- …Sciences, Engineering or related field plus 9 years of SAS programming experience in a clinical trial environment. MS in the same fields plus 7+ years of SAS ... programming experience in a clinical trial environment. Department Required Skills & Experience Excellent interpersonal, negotiation, and collaboration skills.… more
- Vitalief (New Brunswick, NJ)
- …seeking a dynamic, strategic, and client-facing leader to build and lead our Clinical Trial Budgeting and Coverage Analysis Services. This role combines hands-on ... serve as the Subject Matter Expert (SME) and leader for Vitalief's clinical trial budgeting and coverage analysis outsourcing services. + Design, launch, and… more
- IQVIA (Parsippany, NJ)
- …owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... and uphold GCP, SOP, and local regulatory standards. **_Two years of clinical trial management experience is required within a role that is accountable for… more
- Merck (Rahway, NJ)
- …exposure to clinical drug development with emphasis on key elements of clinical trial planning, execution, data analysis and reporting of clinical ... 5 years. **Required Skills:** Clinical Development, Clinical Research, Clinical Sciences, Clinical Trial Planning, Clinical Trials, Clinical … more
- IQVIA (Parsippany, NJ)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. *… more
- Mallinckrodt Pharmaceuticals (Bridgewater, NJ)
- …policies. Research & Development Support: + Provide legal counsel on clinical trial agreements, investigator-initiated studies, and collaborations with academic ... Job Title Associate General Counsel, Advertising & Promotion / Clinical Development Requisition JR000015569 Associate General Counsel, Advertising &… more
- Bristol Myers Squibb (Madison, NJ)
- …projects + Efficiently plans, coordinates, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects + ... BMS R&D pipeline. This role may report into Director, Clinical Data Management or Associate Director, ...functional study team members to ensure on-going review of trial data currency, quality and completeness + Represents DM… more
- ThermoFisher Scientific (Bridgewater, NJ)
- …patient recruitment strategies and the implementation of digital and decentralized clinical trial solutions. + Proven experience providing protocol review ... of Patient-First technology solutions, supporting future innovation and advancing patient-centric clinical trial methodologies. At Thermo Fisher Scientific, we… more
- Merck (Rahway, NJ)
- …Engineering or related field plus 9 years SAS programming experience in a clinical trial environment. + MS in Computer Science, Statistics, Applied Mathematics, ... plus 7 or more years SAS programming experience in a clinical trial environment. **Department Required Skills and Experience:** + Excellent interpersonal skills… more
- Bristol Myers Squibb (Madison, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . Job Description The Associate Director, RBQM - HOCT, ICN will mainly be responsible for ... effective risk and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and establish a feedback loop to… more
- Sanofi Group (Morristown, NJ)
- …such as population pharmacokinetics (PPK), PK/PD, exposure response, model-based meta-analysis, clinical trial simulations and disease progression modeling to ... **Job Title:** Associate Director Quantitative Data Modeling **Location:** Morristown, NJ...translational and population PK modeling, PK/PD modeling, exposure-response modeling, clinical trial simulation, drug-disease modeling, PBPK modeling,… more
- Merck (Rahway, NJ)
- …Atherosclerosis, Cardiology Clinical Research, Cardiovascular Diseases, Clinical Development, Clinical Studies, Clinical Trial Designs, Clinical ... Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Statistical Project Leader ( Associate Director) **Location:** Morristown, NJ Cambridge, MA __ **About the Job** Join the engine of Sanofi's mission - ... and Decision Science (EGDS) group** at Sanofi unites Biostatistics, Clinical Statistical Modeling, and Real-World Evidence to revolutionize data-driven decision… more
