Clinical Trial Associate: Average Salary in Boston, MA in 2024

Maintain the Trial Master File all clinical projects. Keep abreast of SOPs, Good Clinical Practice (GCP) and ICH guidelines as well as state and federal laws and ethical standards. Assemble and distribute regulatory binders to clinical sites. Draft and/or assist with preparation of trial-related doc...

Maintain the Trial Master File all clinical projects. Keep abreast of SOPs, Good Clinical Practice (GCP) and ICH guidelines as well as state and federal laws and ethical standards. Assemble and distribute regulatory binders to clinical sites. Draft and/or assist with preparation of trial-related doc...

Responsible for assisting and providing support to the members of the clinical operations project team to facilitate the operational execution of the clinical trial processes in accordance with regulatory guidelines and ICH/GCP standards. Manages trial-related documents in the Veeva Vault Trial Mast...

The Human-centered AI team in Digital Health Oncology R&D is looking for an Associate Director of Data Science to specialize in the development of novel digital endpoints using data science, statistical learning, and innovative machine learning methods on multi-modal datasets including clinical ...

The Clinical Trials Manager (CTM) is responsible for leading the execution of clinical studies on schedule and on budget. A minimum 5+ years of experience or demonstration of equivalent capability in a Clinical Trials Manager role. Accountable for project related efforts for the delivery of studies ...

The Clinical Trials Manager (CTM) is responsible for leading the execution of clinical studies on schedule and on budget. A minimum 5+ years of experience or demonstration of equivalent capability in a Clinical Trials Manager role. Accountable for project related efforts for the delivery of studies ...

The Clinical Trials Manager (CTM) is responsible for leading the execution of clinical studies on schedule and on budget. A minimum 5+ years of experience or demonstration of equivalent capability in a Clinical Trials Manager role. Accountable for project related efforts for the delivery of studies ...

This role will process clinical documents for anonymization and/or pseudo anonymization in support of Health Canada's PRCI process, EMA policy 0070, EU Clinical Trial Regulation (CTR) and other disclosures of clinical documents that must be redacted or otherwise anonymized to support results posting...

The Clinical Trial Manager, Site Start-up role plays a significant contribution to the clinical trial execution and ability to meet the corporate study goals for the Company clinical programs. The Clinical Trial Manager, Site Start-up will lead internal process improvements related to study start up...

The Clinical Trial Manager, Site Start-up role plays a significant contribution to the clinical trial execution and ability to meet the corporate study goals for the Company clinical programs. The Clinical Trial Manager, Site Start-up will lead internal process improvements related to study start up...

Clinical Trial Assistant or Associate Clinical Trial Manager to join our client based in Waltham. Clinical Trial Assistant / Associate CTM. Responsible for trial related activities from startup to close-out of a clinical trial in close collaboration with internal stakeholders and CROs. Drive the ope...

The Clinical Trials Manager (CTM) is responsible for leading the execution of clinical studies on schedule and on budget. A minimum 5+ years of experience or demonstration of equivalent capability in a Clinical Trials Manager role. Accountable for project related efforts for the delivery of studies ...

The Clinical Trials Manager (CTM) is responsible for leading the execution of clinical studies on schedule and on budget. A minimum 5+ years of experience or demonstration of equivalent capability in a Clinical Trials Manager role. Accountable for project related efforts for the delivery of studies ...

The Clinical Trials Manager (CTM) is responsible for leading the execution of clinical studies on schedule and on budget. A minimum 5+ years of experience or demonstration of equivalent capability in a Clinical Trials Manager role. Accountable for project related efforts for the delivery of studies ...

The Clinical Trials Manager (CTM) is responsible for leading the execution of clinical studies on schedule and on budget. A minimum 5+ years of experience or demonstration of equivalent capability in a Clinical Trials Manager role. Accountable for project related efforts for the delivery of studies ...

This is a contract job opportunity.Position: Financial Data Scientist 0Location: Remote job - prefer local to Durham NC but open to candidates in EST and CSTSchedule: 8 am - 5 pm M-FProjected duration: 6 months + potential for permJob code:CVDJP Benefits are available Highlights:.Large volumes of da...

The Clinical Trial Manager, Site Start-up role plays a significant contribution to the clinical trial execution and ability to meet the corporate study goals for the Company clinical programs. The Clinical Trial Manager, Site Start-up will lead internal process improvements related to study start up...

The Clinical Trial Manager, Site Start-up role plays a significant contribution to the clinical trial execution and ability to meet the corporate study goals for the Company clinical programs. The Clinical Trial Manager, Site Start-up will lead internal process improvements related to study start up...

The Clinical Trial Manager, Site Start-up role plays a significant contribution to the clinical trial execution and ability to meet the corporate study goals for the Company clinical programs. The Clinical Trial Manager, Site Start-up will lead internal process improvements related to study start up...

Working closely with our service providers, central laboratories and other specialized clinical trial vendors to support clinical sample and central imaging/ePRO reconciliation activities. Serve as the key point of contact for sample management for the clinical trial teams and cross functional depar...

As a core member of the Clinical Operations Team and leader of the Clinical Trial Team, aligns clinical trial team with organizational goals, Clinical Operations Team, and/or Global Program Strategy Team. Leads the development of the clinical trial strategy while accountable for successful project e...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...

The Clinical Trial Associate (CTA) will administer, maintain, and coordinate the logistical aspects of clinical trials and participate in a variety of clinical activities to support and facilitate the efficient conduct of Agios’ clinical research programs. Clinical Trial Associate, Clinical Operatio...

The Clinical Trial Associate (CTA) provides clinical trial coordination support to Project Teams for assigned. As a Clinical Trial Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Assist the Clinical Operations...

The Clinical Trial Manager, Site Start-up role plays a significant contribution to the clinical trial execution and ability to meet the corporate study goals for the Company clinical programs. The Clinical Trial Manager, Site Start-up will lead internal process improvements related to study start up...