- 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
- The Antibody Society (Princeton, NJ)
- …surveillance and escalation management. Cross-functional Collaboration Collaborate with Trial Management, Medical, Biomarker Operations, Clinical Programming, ... Serve as a portfolio-level lead for external data quality and clinical data-related operational strategy. Drive consistency of processes, quality expectations, and… 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
- 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
- Syneos Health, Inc. (New York, NY)
- …solutions organization built to accelerate customer success. We translate unique clinical , medical affairs and commercial insights into outcomes to address modern ... market realities. Our Clinical Development model brings the customer and the patient...and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is… more
- TANNER & ASSOC INC (Trenton, NJ)
- …booth activities Provides recommendations to Medical Affairs Teams on Phase IV clinical trial design regarding promotability of potential data/claims Works with ... Associate Director, Regulatory Affairs, Advertising & Promotion-New Jersey...closely with Marketing Brand Teams, Legal, Medical Affairs and Clinical Research in the development of advertising and promotional… more
- Princeton Legal Search Group, LLC (Trenton, NJ)
- …Collaboration Agreements: The Central Collaboration Agreements that include Master Clinical Trial Agreements, Subaward Agreements, Shared Resources Agreements, ... The Office of Innovation and Commercialization. Responsibilities: The Vice President, Associate General Counsel reports directly to the Senior Vice President, Deputy… more
- DBV Technologies (Trenton, NJ)
- …EU, and Canadian health agency regulatory standards Well-versed in scientific and clinical trial knowledge, documents, and vocabulary Proficiency in Microsoft ... Description : The Associate Director US Regulatory Affairs - Advertising &...approval of materials and projects. In this capacity, the Associate Director collaborates closely with cross-functional partners, including Medical… more
- Syneos Health, Inc. (Trenton, NJ)
- …solutions organization built to accelerate customer success. We translate unique clinical , medical affairs and commercial insights into outcomes to address modern ... market realities. Our Clinical Development model brings the customer and the patient...and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is… 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
- Taiho Oncology (Princeton, NJ)
- …sciences is preferred. Knowledge, Skills, and Abilities: + 2 years of relevant clinical trial support or site management experience in the pharmaceutical, ... team cultivating growth and learning. Position Summary: The Study Associate (SA) I is responsible for operational study support...to multi-task and effectively prioritize in order to ensure clinical trial goals. + Recognize potential obstacles… more
- System One (Basking Ridge, NJ)
- Job Title: Clinical Study Associate I Location: Basking Ridge, NJ Type: Contract - 1 year Contractor Work Model: Hybrid - must be able to go onsite 1-4 ... the life sciences industry? Joule is currently seeking a Clinical Study Associate to join an industry-leading...This is a high-visibility role where your expertise in Trial Master File (TMF) integrity will directly support the… more
- Bristol Myers Squibb (Princeton, NJ)
- … development, the position is responsible for various aspects of ongoing clinical trial program-related activities within the relevant therapeutic area. These ... their personal lives. Read more: careers.bms.com/working-with-us . **Summary** The Associate Director of Clinical Science plays a...may be assigned. + Acquires and utilizes knowledge of clinical trial design to develop or oversee… 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
- Bristol Myers Squibb (Princeton, NJ)
- …your application should be directed to Chat with Ripley. R1597891 : Associate Director, Oncology Clinical Biomarker Asset Lead, Translational Development ... will offer the greatest possible benefit to patients. **Position Summary** The Clinical Biomarker Asset Lead role will be responsible for development and execution… more
- IQVIA (New York, NY)
- …bring breakthrough treatments to patients faster._ **Job Overview** We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key ... role in ensuring the successful execution of clinical trials. In this position, you will be responsible...essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File… more
