Clinical Trial Associate: Average Salary in California in 2024

Collaborate with Clinical Trials Manager (CTM) and Clinical Research Associates (CRAs) to resolve clinical trial documentation issues. Responsible for clinical trials administration to ensure the most effective and efficient conduct of clinical research studies. Support the Clinical Operations teams...

A company is looking for a Clinical Trial Associate. ...

As a Senior Clinical Trial Associate (Sr. Review study plans, including Clinical Monitoring, Communication, Project Management, and electronic Trial Master File (eTMF) Management. Clinical Trials Design and Management Certificate). Bachelor’s degree, preferably in biological sciences, health care ma...

A company is looking for a Clinical Trials Associate. ...

CTM, Clinical Operations and will be responsible for supporting the day-to-day operations of one or more phase 1-3 clinical trials including trial start up, conduct and close-out activities. Coordinate tracking of a clinical trial(s) under the oversight of the Clinical Trial Management. Senior Clini...

A company is looking for a Global Clinical Trial Associate - Home-Based in the US or Canada. ...

As a Clinical Trials Associate in Oncology, you will play a crucial role in supporting the planning, coordination, and execution of clinical trials within the oncology portfolio. We are seeking a detail-oriented and highly motivated Clinical Trials Associate to join our oncology research team. Previ...

The Clinical Trial Assistant (CTA) supports study teams in the planning, designing, executing, monitoring, and reporting of clinical trials. To assist project teams with trial progress tracking by updating the Clinical Trial Management systems. Clinical Trial Assistant in life sciences industry pref...

Clinical Trial Manager/Associate Director manages the operational activities of assigned clinical programs. Responsible for the review and oversight oftasks in study monitoring plans foroperations and all operational activities associated with clinical trials. Coordinate and plan for availability of...

Clinical Operations plays a key role in ensuring all clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of products. Clinical Trial Manag...

The Clinical Trial Associate will be located in-office and, under supervision, will support the Clinical Affairs department in the conduct of clinical research studies (IDE/Post-Approval/Post-Market) sponsored by our client. This person will support the clinical studies by assembling and distributin...

If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Adheres to GCP and compliance regulations for clinical trials. Minimum one (1) year of experience in clinical trials protocols involving research methodology/research study design, and hypothesis testing; OR. May part...

We are seeking a Clinical Trials Management Associate - I for a very important client Must meet all requirements for Clinical Project Assistant position and have demonstrated proficiency in all relevant areas Provides administrative assistance in site selection, study implementation and ongoing coor...

If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Adheres to GCP and compliance regulations for clinical trials. Minimum one (1) year of experience in clinical trials protocols involving research methodology/research study design, and hypothesis testing; OR. May part...

Clinical Trials Management Associate - I*. Clinical Trials Management Associate - I*,. Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable. Must meet all requirements for Clinical Project Assistant position and have demonstrated pr...

Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable. Must meet all requirements for Clinical Project Assistant position and have demonstrated proficiency in all relevant areas. Under supervision may assist in review of protocols, i...

Our pharmaceutical client is recruiting for a Clinical Trial Management Associate to join their growing team. Support review of protocols, informed consents, case report forms, monitoring plans, abstracts, presentations, manuscripts and clinical study reports. ...

Clinical Trials Management Associate - I*. Clinical Trials Management Associate - I*,. Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable. Must meet all requirements for Clinical Project Assistant position and have demonstrated pr...

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. ...

Collaborate with Clinical Trials Manager (CTM) and Clinical Research Associates (CRAs) to resolve clinical trial documentation issues. Responsible for clinical trials administration to ensure the most effective and efficient conduct of clinical research studies. Support the Clinical Operations teams...

Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is be able to participate in departmental or interdepartmental strategic initiative under general supervision. Must meet all requirements for Clinical Project Assistant position and have demon...

Job Title: Clinical Trials Management Associate - I*. Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable. Must meet all requirements for Clinical Project Assistant position and have demonstrated proficiency in all relevant areas. ...

The Clinical Trial Associate (CTA) provides administrative support to the Clinical Operations Department. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising...

Job title: Clinical Trials Management Associate - I*. Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable. Must meet all requirements for Clinical Project Assistant position and have demonstrated proficiency in all relevant areas. ...

Clinical Operations plays a key role in ensuring all clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of products. Clinical Trial Manag...