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The Senior Clinical Trial Administrator (CTA) is responsible for performing a variety of research, database, and clerical duties of a complex and technical nature in support of multiple clinical trials. This position also provides administrative support to clinical teams by reviewing vendor invoices for accuracy against budget, tracking vendor payments in compliance with
Posted 1 day ago
Under the direction and as requested by the Lead Clinical Research Associate of assigned studies, the Clinical Research Associate (CRA) Ensures assigned studies are conducted in compliance with the currently approved Protocol(s)/Amendment(s), SOPs, Code of Federal Regulations (CFR), Good Clinical Practice (ICH GCP), and local or country regulations Participates in Investi
Posted 3 days ago
Responsible for leading, implementing, and managing a dedicated flexible sourcing initiative specific to client's needs. Establish Key Performance Indicators (KPIs), and Governance/Steering Committee/s. Act as primary liaison to hiring managers and candidates. Ensure that client's needs, expectations and goals are met and exceeded. Craft and Implement program and quality
Posted 11 days ago
The PRC Legal Regulatory Reviewer tasks include reviewing claims within promotional materials to ensure alignment with applicable laws and regulations. EXPERIENCE PharmD preferred 10 + years of Promotional Review experience in the Pharma or Biotech Industry Experience with Veeva vault platform preferred REQUIRED SKILLS Ability to understand and interpret clinical data Gen
Posted 14 days ago
We are currently searching for a skilled professional to join a well known client's team as a remote Study Planning and Feasibility Manager. Their work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity. The Study Planning & Feasibility Manager within the Clinical Development; Strategic Business Operati
Posted 25 days ago
Work with the Global and US regulatory & commercial team to support pipeline advancement, on market strategy/execution and FDA approval and post marketing commitments for parenteral nutrition (PN) products, providing medical / scientific support. Mentor, manage, and ensure development of the PN Medical Affairs Team. Lead team to support medical content development and rev
Posted 28 days ago
Ensure efficient study execution, including oversight of CROs, vendors and consultants that are involved with the clinical trial Responsible for oversight and project management of individual studies as assigned Offer advice related to study milestones and ensure accurate tracking and reporting of study metrics and timelines. Risk identification and mitigation efforts and
Posted 29 days ago
OVERVIEW We are currently searching for a skilled professional to join a well known client's team as a Scientist III 509796 in Remote or Ridgefield, CT (Hybrid). Their work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity. RESPONSIBILITIES Duties and responsibilities Apply advanced statistics and mach
Posted 1 month ago
Conduct site qualification, initiation, remote and interim monitoring and study closeout visits for pediatric and adult nutrition and Phase 1 4 studies in accordance with the protocols, federal regulations, Good Clinical Practices (GCPs), ICH Guidelines, and Company Standard Operating Procedures (SOPs) and business processes. Set up study site management in Clinical Trial
Posted 1 month ago
Provide scientific expertise necessary to support the data quality and delivery of clinical studies and programs. Work directly with the Sr Director, Clinical Sciences to implement activities supporting clinical development plans for assigned program(s) including o Review, query, analyze, and interpret emerging clinical trial data o Present, review, and interpret the full
Posted 1 month ago
Provide quality leadership and direction to Sponsor's R&D stakeholders on GCP related activities/issues and act as GCP expert/consultant for R&D colleagues. Act as a Clinical Compliance member of clinical study teams for relevant Therapeutic Areas. Develop strong relationships with R&D personnel across functions and teams providing coaching and compliance guidance as need
Posted 2 months ago
Providing strategic leadership and demonstrating accountability for the clinical pharmacology programs supporting Phase 1 4 clinical development for development compounds Representing the department and providing subject matter expertise on cross functional project teams Developing and maintaining collaborative working relationship with colleagues within and outside the d
Posted 2 months ago
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