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
$90k - $125k
...and to each other is based on the humanity that we share. Senior Clinical Trial Associate Position Overview Ovid Therapeutics is seeking a detail-oriented and organized Senior Clinical Trial Associate (CTA) to support the execution of clinical studies and the day-...SeniorWork at officeFlexible hours- ...Role: Clinical Trial Associate supporting the execution and management of ophthalmology clinical studies, under supervision. Responsibilities Assisting with study planning, protocol and documentation development, IRB submissions, site communication, monitoring support...SeniorRemote work
- A biotechnology organization is seeking a skilled Clinical Trial Associate to join their innovative team remotely. The ideal candidate will have over 3 years of experience in clinical trial coordination and documentation management. This full-time contract position involves...SeniorRemote jobFull timeContract workWork at office
$75k - $130k
...Job Description Join us as Project Manager Clinical Supplies to manage the end-to-end supply chain for clinical trials, ensure timely and efficient distribution of trial... ...studies. • We are currently seeking Associate Project Managers, Project Managers, and Sr. Project...SeniorContract workTemporary workWork at officeRemote workWork from home$56.4k - $95.9k
...change and accelerate progress. Our Clinical Solutions team members act with a... ...activities, as assigned by the Clinical Trial Supplies Manager (CTSM) or Project... ...clearance, supply and return). The Senior Clinical Trial Supplies Associate operates independently, with...SeniorContract workWork at officeFlexible hours$60k - $68k
...major depressive disorder, agitation associated with dementia due to Alzheimer’s disease... ...AxsomeTherapeutics isseekingaClinical Trial Associate (CTA)thatisresponsible forsupporting the... ...to successfully develop and implement clinical trials across its product portfolio and...Local areaRemote work3 days per week- Job Description The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of clinical trials under the direction of the Vice President, Development Operations, with day‑to‑day guidance from the assigned Study Lead. The CTA plays a key...Work at office
- ...research institute, seeks a Principal Investigator/Senior Research Epidemiologist/Biostatistician for its Center for Clinical Research in Research Triangle Park, NC, or as a... ...centers for multi-site clinical studies, guide trial design and data analysis, and collaborate with...SeniorRemote job
- ...Academic Scholar - Pediatric Pulmonologist; Clinical Assistant/Associate/Full Professor Position Title: Academic Scholar‑Pediatric Pulmonologist... ...Leadership opportunities include program growth, clinical trials expansion, quality improvement, and regional/national...TraineeshipFlexible hours
$38 - $40 per hour
...from Baim Institute for Clinical Research Director,... ...Sr. Clinical Research Associate/Field Monitor Contractor... ...-house CRA Comply with Trial Master File (TMF) document... ...study specific needs. Seniority level Seniority level Mid... ...Clinical Trial Administrator (CTA) - Clinical Research...SeniorPart timeFor contractorsInterim roleRemote workWork from home10 hours per week$77k - $202k
...ServicesSpecialismOperationsManagement LevelSenior AssociateJob Description & SummaryThe OpportunityAs a Provider Clinical Operations Consultant, Senior Associate you will support healthcare provider clients in clinical operations modernization, helping shape work across...SeniorFull timeH1bShift work- ...A leading global CRO is seeking a Senior Lead Clinical Data Manager to act as the primary client contact and oversee clinical trial databases. With over 10 years of experience in Clinical Data Management, the ideal candidate will lead studies while collaborating with international...SeniorRemote work
$70k - $78k
...Clinical Safety Reviewer / Senior Clinical Safety Reviewer This role is subject to a flexible hybrid work arrangement requiring a minimum... ...the dissemination of safety information to the Clinical Trial Affairs (CTA) team members and clinical trial core team members, as...Temporary workWork at officeFlexible hours2 days per week1 day per week- ...recording laboratory tests. Assists in coordinating organization of patient needs including preparation and organization of patient clinic charts. Job Responsibility #1.Leads and guides Medical Assistants in the performance of duites. #2.Provides input for the...SeniorHourly pay
- ...Oruka Therapeutics Inc in the United States seeks a senior Data Manager to lead clinical data management across trials, ensuring high-quality, compliant data under ICH-GCP and SOPs. You will engage CROs and vendors for database start-up, cleaning and locking, while keeping...Senior
- ...will be valued and respected. Summary: The Clinical Specialist will be responsible for... ...Sales Manager, leading clinical evaluations, trials and installations, in addition to collecting... ...Clinical Specialist will report to the Senior Clinical Services Manager. This position...SeniorHourly payCasual workWorldwideNight shift
$165k - $185k
Arbor Biotechnologies, a clinical stage, next-generation gene editing company based in... ...keep reading. Why this role matters. The Senior Clinical Trial Manager will lead day-to-day clinical... ...such as pre-IND, IND, Scientific Advice, CTA, or similar filings. Strong knowledge...SeniorWork at officeRemote work$30 - $33.65 per hour
...Overview Join to apply for the Senior Medical Assistant role at Sana . This range is provided... ...patient care coordination and clinical support. The majority of the role (80-90... ...setting. High school diploma or GED required; associate degree preferred. Medical Assistant...SeniorHourly payFull timeRemote workFlexible hoursShift work- ...BridgeBio Pharma seeks a Sr. Clinical Research Associate/Clinical Trial Manager to support timely conduct of studies from planning through close-out on a remote US basis. You will collaborate with Clinical Operations to ensure adherence to protocols, GCP, SOPs and regulatory...SeniorRemote work
- ...Responsibilities Oversee global Phase 3 clinical trials and BLA filings Develop and execute integrated clinical trial programs including protocol design Provide medical oversight for new and ongoing studies Work cross-functionally with Medical Affairs, Regulatory, Commercial...Senior
- ...Senior Clinical Data Manager Small CRO | Full time | Remote, Canada or US Our client is a well established small CRO known for providing top... ...3 years of independent lead experience, and hands on oncology trial experience. Key responsibilities Manage data processing tasks...SeniorFull timeRemote work
- Pulmovant is seeking an Executive Assistant to support senior leaders in the clinical and clinical trial/program groups. The role requires exceptional organization, problem solving and the ability to handle multiple workstreams in a fast-paced startup environment. The successful...Senior
- Karius, a life sciences company focused on infectious diseases, seeks a Sr. Clinical Research Associate to oversee advanced site monitoring across clinical programs, ensuring adherence to ICH-GCP and sponsor procedures. The role emphasizes independent site ownership and...SeniorRemote job
- ...Senior Clinical Project Manager / Global Study Manager Global Clinical Development Position Summary The Senior Clinical Project... ...provides strategic and operational leadership for global clinical trials. This role is responsible for end-to-end study execution,...Senior
- ...Senior Manager, Clinical Data Management at Takeda Overseeing a team responsible for developing and optimizing clinical data management processes. Primary objectives include ensuring clinical trials are conducted efficiently, compliant with regulatory standards, and aligned...SeniorRemote workFlexible hours
- Takeda is seeking a Lead Clinical Study Manager to oversee clinical trial strategy and execution across development programs. This role ensures studies comply with ICH GCP and regulatory standards, stay on schedule, and meet budgets. Responsibilities include trial planning...SeniorRemote job
- Alpheva is seeking a senior clinical research expert to support AI evaluation projects centered on study protocols, endpoints, bias, safety reporting, and trial interpretation. This is remote, project-based contract work with scope, hours, and assignments determined by...SeniorRemote jobContract work
- Precision Medicine Group is seeking a Clinical Trial Manager/Senior Clinical Trial Manager to lead the planning, conduct, and oversight of operational aspects of clinical studies from a remote location in the United States. You will work as the primary client contact and...SeniorRemote job
- Arbor Biotechnologies seeks an experienced Senior Clinical Trial Manager to lead day-to-day operations for early-phase gene-editing studies. You will manage sites, CROs, vendors, budgets, and trial timelines, partnering with internal teams to ensure smooth execution. Reporting...SeniorRemote job
- NYU Grossman School of Medicine is seeking a Senior Clinical Research Coordinator to oversee a range of Eosinophilic Gastrointestinal Diseases (EGID) studies. This role demands effective management skills to ensure compliance and progress through all phases of studies....SeniorWork at office
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