Senior Clinical Trial Associate (CTA)
$40 - $45 per hourPlanet Pharma
This range is provided by Planet Pharma. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $40.00/hr - $45.00/hr Join a growing and innovative biotechnology organization developing next-generation therapies across multiple therapeutic areas. This is an exciting opportunity for a skilled and organized Clinical Trial Associate who thrives in a collaborative, detail-oriented environment. We’re seeking someone proactive, reliable, and passionate about delivering high-quality clinical operations support — someone who takes ownership, communicates effectively, and keeps studies on track from start-up through completion. What You’ll Do Coordinate study start-up tasks, submissions, and documentation for IRB/EC approvals Manage and maintain Trial Master Files (TMF) and Investigator Site Files (ISF) Track budgets, purchase orders (POs), invoices, and site payments Assist with IVRS/IRT setup and study tracking systems Prepare and distribute study materials, Investigator Brochures, and patient documents Organize and participate in Investigator and Study Team meetings Maintain study contact lists, correspondence, and document trackers Support development and review of SOPs and clinical quality documentation Ensure adherence to ICH-GCP and all regulatory requirements What We’re Looking For 3+ years of experience as a Clinical Trial Associate (CTA) Proven experience with study start-up, TMF management, and IVRS Experience handling budgets, trackers, and clinical documentation systems Working knowledge of Veeva Vault eTMF Understanding of IRB and regulatory submission processes Proficiency in Microsoft Word, Excel, and PowerPoint Exceptional organization, attention to detail, and communication skills Contract length: 6+ months (potential to extend) Schedule: Full-time, standard business hours EST Location: 100% Remote (must reside in Eastern Time Zone) Seniority level Mid-Senior level Employment type Contract Job function Research, Project Management, and Quality Assurance Industries: Biotechnology Research, Pharmaceutical Manufacturing, and Medical Equipment Manufacturing Medical insurance, Vision insurance, and 401(k) benefits available. #J-18808-Ljbffr Planet Pharma
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About the role. The Senior Clinical Trial Manager will lead day-to-day clinical trial operations for assigned early-phase studies of our gene-editing... ...submissions, such as pre‑IND, IND, Scientific Advice, CTA, or similar filings. Strong knowledge of GCP, ICH guidelines...SeniorWork at officeRemote work- Worldwide Clinical Trials is seeking a Clinical Data Associate II for a remote role based in Argentina. You will contribute to day-to-day data management, data cleaning, UAT, and study documentation, collaborating with global teams across time zones. We value attention...Remote jobWorldwide
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Provide medical direction and oversight for clinical trials, including emergency cover. Partner with GCO on business development, proposals, and feasibility. Qualifications: MD/DO with relevant fellowship and board certification. 3-10 years of clinical research experience...SeniorRemote jobContract work- Montefiore Medical Center in Bronx, NY seeks a Cancer Clinical Trials Senior Research Associate to support the conduct of clinical trials under GCP. This role functions independently as the lead Research Associate for the disease group, mentoring junior staff and reviewing...Senior
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$137k - $215.27k
...For our client, we are seeking a Senior Manager, Clinical Data Management to join the team of a leader in the Pharmaceuticals & Biotech space.... ...will guide a clinical data management team supporting complex trials, with a focus on data quality, regulatory compliance, and...SeniorRemote workVisa sponsorshipFlexible hours- Generate:Biomedicines is seeking a senior Clinical Operations leader to shape and oversee the strategy for programs in development. You will partner with cross-functional teams to drive protocols, safety reports, investigator brochures, and regulatory submissions. The role...Senior
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