Clinical Trial Associate
Integrated Resources
Clinical Trial Associate
Responsible for assisting and providing support to the members of the clinical operations project team (i.e. Clinical Project Managers, Associate Directors, or Directors), in order to facilitate the management of pre- and post-approval clinical trial processes including quality review and document prep. The CTA performs work within established protocols under general supervision.
• Main priority is candidate is competent and able to do this role, and start ASAP.
• Candidate needs to be able to jump in and do work well.
• Candidate will be working on documentation review in QC.
• Candidate must understand clinical trial process and documentation.
• Must have SOME experience in clinical trial process and documentation.
• Willing to see new graduates as long as they have some experience.
$90k - $124k
Job DescriptionWe are seeking a motivated and detail-oriented Clinical Trial Associate (CTA) to support the execution of clinical studies within our Clinical Operations team. In this role, you will contribute to key trial activities and ensure that study components are...Suggested$115k - $159k
Job DescriptionWe are seeking a detail-oriented and proactive Sr. Clinical Trial Associate (Sr. CTA) to support the successful execution of clinical studies within Clinical Operations. In this role, you will partner closely with study leads and cross-functional teams to...Suggested$75k - $140k
...Clinical Trial Associate Waltham, MA Clinical Trial Associate/ Senior Clinical Trial Associate Skyhawk Therapeutics is seeking a highly motivated CTA to provide administrative and operational support to Clinical Operations. Responsibilities (including, but...SuggestedWork at office$86k - $105k
...Senior Clinical Trial AssociateWaltham, MACompany Overview:Dyne Therapeutics is focused on delivering functional improvement for people... ...families and communities.Role Summary:The Senior Clinical Trial Associate (CTA) is a key member of the Clinical Operations team...SuggestedWork at officeLocal area$115k - $140k
Senior Clinical Trial Associate (Sr. CTA) Burlington, MA Who We Are MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting‑edge technologies including optogenetics, in vivo physiology...SuggestedTemporary workWork at officeWorldwideFlexible hours$90k - $100k
Why join Cardurion Pharma? We are a clinical-stage biotechnology company discovering and developing new therapeutic approaches to treat... ...to join Cardurion's Clinical Operations team as Sr. Clinical Trial Associate (Sr. CTA). Reporting to the Senior Manager, Clinical...Contract workTemporary workWork experience placementFlexible hoursShift work3 days per week$108k - $132k
...the next wave of therapies for cancer patients. The Company’s clinical-stage pipeline includes its lead program, a PD-1 x VEGF bispecific... ...of Clinical Operations to support the conduct of clinical trials. You will partner with the Clinical Study Lead to ensure studies...Contract workTemporary workTrial periodFlexible hours$58k - $76.67k
Clinical Laboratory Process Development Associate I Join to apply for the Clinical Laboratory Process Development Associate I role at Broad Institute of MIT... ...research to population genomics, from cancer clinical trials to understanding cell circuitry. We are expanding...Full timeLocal areaImmediate startFlexible hours- Cardurion Pharmaceuticals in Massachusetts is seeking a Sr. Clinical Trial Associate to support operational planning and execution for Global Phase 1-3 studies. You will coordinate study documents, vendor activities, and TMF quality reviews, working with cross-functional...3 days per week
$110k - $120k
...Senior Clinical Trial AssociateBoston, MassachusettsOlema Oncology is a clinical-stage biopharmaceutical company committed to transforming... ...Senior Clinical Trial AssociateAs the Senior Clinical Trial Associate reporting to the Senior Manager, Clinical Trial Leader, you will...Contract workWork at officeFlexible hours$88k - $100k
...Our Science: Advancing Cancer Immunotherapies Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal... ...patients. Learn more: Position Summary: The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3...Work at office- ...Clinical Research CoordinatorResponsible for coordinating and performing the collection, distribution and storage/archival of data/study... ...supply generated for assigned studies during clinical research trials. Ensure that the assigned trials stay on track with applicable...
$20 - $23.1 per hour
...clinician.Responsible for cross coverage when needed.May assist clinical trainer in training new MAs and Gap Interns and retraining... ...Research Responsibilities include but not limited to:Lead clinical trials on various topical products and creams.Meet with patients at visit...Hourly payFull timeInternshipWork at officeLocal area$68.88k - $94.95k
...Clinical Trial Associate Watertown, Massachusetts, United States This individual will assist the clinical operations team in the day-to-day operations, study start up, execution, and closeout of trials across the portfolio. Responsibilities Support the...Fixed term contract- ...Verastem Oncology Clinical Trial Document ManagerAt Verastem Oncology, we address urgent needs of patients living with cancers driven by RAS/MAPK pathway mutations, a key driver of tumor growth and treatment resistance. FDA approval of AVMAPKI FAKZYNJA CO-PACK delivered...Contract work
$152.6k - $283.4k
Job Description Summary#LI-HybridLocation: CambridgeThe Clinical Sciences Associate Director may provide clinical leadership and strategic input for... ...are met.Lead a global cross functional Clinical Trial Team (CTT) to ensure all trial deliverables are met; set stretch...Full time- Olema Oncology is seeking a Senior Clinical Trial Associate to provide comprehensive administrative and operational support across in-house and outsourced trials. You will coordinate with internal teams, vendors and investigator sites, contributing to TMF maintenance and...Work at office
$78 - $86 per hour
A leading biotechnology firm is seeking a mid-senior level Account Executive to manage clinical trial processes in Cambridge, MA. Candidates should have over 3 years of Clinical Operations experience, a strong grasp of Good Clinical Practices, and excellent communication...Hourly pay- Job Summary The Clinical Trial Associate (CTA) is a core member of the Clinical Affairs team and is responsible for independently supporting the planning, execution, and closeout of domestic and international medical device clinical trials. This role operates with a high...
$78 - $86 per hour
...Executive at Stratacuity: Proven Scientific Placement Sr. Clinical Study Associate III This position requires 3x per week onsite in Cambridge... ...Manufacturing What You’ll Do Support day‑to‑day clinical trial activities in partnership with the Clinical Study Manager and...Contract work$71k - $96k
Responsibilities Job Summary The Senior Clinical Studies Associate supports the planning, execution and oversight of clinical studies throughout... ...Ensure timely filing, quality review, and completeness of Trial Master File (TMF) documentation. Assist with development and...Work experience placementWork at officeLocal areaRemote work- ...Description Job Description PROMETRIKA is a full-service clinical research organization (CRO) with extensive experience in clinical... ...and medical device companies of all sizes. The Clinical Trial Associate II (CTA II) supports, coordinates, and implements clinical...Work experience placementWork at office
$17.42 - $21.42 per hour
...skin, cheek swabs, and pheresis products.Establishes effective policies and procedures for obtaining, processing and handling all clinical trial-driven correlative blood and tissue samples.Collaborates with internal and external laboratories processing clinical trial...- Clinical Lab Process Development Associate I- Cell Factory Location: United States, Massachusetts, Burlington Posted: Mar 09, 2026 The Genomics Platform is dedicated to solving the world’s most challenging biomedical problems through continuous development and investment...Full timeLocal area
- ...research projects that are both challenging and complex. In support of continually changing initiatives, the Clinical Laboratory Process Development Associate II is committed to carrying out innovative, high-throughput lab processes and supporting the highest quality research...Full timeLocal areaImmediate startFlexible hours
- ...Clinical Research CoordinatorResponsibilities:Contribute to the development of study-related documents (Clinical protocols, ICFs, IBs,... ...activationsParticipate in the ongoing review and cleaning of clinical trial dataAssist with the management of tracking, logistics, and...Contract work
- ...Preference given to candidates with prior clinical research experience All positions... ...week out of our Boston office. The Data Associate is responsible for the quality control... ...participation in adult oncology clinical trials. The EAMRF provides the necessary support...Full timeImmediate startMonday to Friday2 days per week1 day per week
- Job DescriptionGeneral Summary:The Clinical Development Associate Medical Director will serve as the Medical Lead for clinical trials, working with cross-functional teams on trial strategy, design, execution, and reporting. In addition to oversight and accountability for...Full timeSummer workRemote workFlexible hours2 days per week
$61k - $87k
Relay Therapeutics is looking for a Clinical Project Associate in Cambridge, MA. The role involves coordinating clinical trial operations and supporting compliance with regulatory guidelines. Ideal candidates will have a Bachelor’s degree and at least 2 years of clinical...- Relaytherapeutics is seeking a Clinical Project Associate in Cambridge, Massachusetts. This role involves providing clinical trial coordination support and ensuring compliance with regulatory guidelines. You'll work closely with Clinical Project Managers and CROs, contribute...
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