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ICONMA
Foster City, CA, United States
JOB TITLE: Sr. Clinical Trial Management Associate (Senior CTMA) FUNCTION: Clinical Operations – Biomarker and Bioanalytical Operations POSITION OVERVIEW: Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all Gilead therapeutic areas. Clinical Operations plays a key role in ensuring all Gil
Job Source: ICONMAThe Fountain Group
Foster City, CA, United States
Pay: $62.98 Sr. Clinical Trial Management Associate (Senior CTMA) FUNCTION: Clinical Operations – Biomarker and Bioanalytical Operations POSITION OVERVIEW: Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all therapeutic areas. Clinical Operations plays a key role in ensuring all clinic
Job Source: The Fountain GroupAIC
San Mateo, CA, United States
Innova Solutions is immediately hiring for a Clinical Trials Management Associate - III Please read the information in this job post thoroughly to understand exactly what is expected of potential candidates. Position type: Full time Contract. Duration: 6 months Location: Foster City, CA As a Clinical Trials Management Associate - III, you will
Job Source: AICProfessional Diversity Network
Foster City, CA, United States
JOB TITLE: Sr. Clinical Trial Management Associate (Senior CTMA) FUNCTION: Clinical Operations – Biomarker and Bioanalytical Operations POSITION OVERVIEW: Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all Gilead therapeutic areas. Clinical Operations plays a key role in ensuring all Gilea
Job Source: Professional Diversity NetworkLanceSoft
Foster City, CA, United States
Summary: Contract Role 6 Months + POSITION OVERVIEW: Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all Company therapeutic areas. Clinical Operations plays a key role in ensuring all Company clinical trials are performed in accordance with applicable SOPs, company policies and regulato
Job Source: LanceSoftApTask
Foster City, CA, United States
About Client: The client is a leading American biopharmaceutical company. It specializes in the discovery, development, and commercialization of innovative therapeutics, particularly in antiviral drugs for HIV, hepatitis B, hepatitis C, and influenza. Known for key products like Truvada, Biktarvy, and Sovaldi, it invests heavily in research and de
Job Source: ApTaskICONMA
San Mateo, CA, United States
JOB TITLE: Sr. Clinical Trial Management Associate (Senior CTMA) FUNCTION: Clinical Operations - Biomarker and Bioanalytical Operations POSITION OVERVIEW: Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all Gilead therapeutic areas. Clinical Operations plays a key role in ensuring all Gilea
Job Source: ICONMAThe Fountain Group
Foster City, CA, United States
Pay: $62.98 Sr. Clinical Trial Management Associate (Senior CTMA) FUNCTION: Clinical Operations – Biomarker and Bioanalytical Operations POSITION OVERVIEW: Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all therapeutic areas. Clinical Operations plays a key role in ensuring all clinic
Job Source: The Fountain GroupSan Mateo, CA, United States
Pay: $62.98
Sr. Clinical Trial Management Associate (Senior CTMA)
FUNCTION: Clinical Operations - Biomarker and Bioanalytical Operations
POSITION OVERVIEW:
Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all therapeutic 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.
You will support other Clinical Operations team members in the start-up, maintenance, and close-out of clinical studies.
You may manage certain components of clinical studies and act as a member of the study team.
You may also manage vendors and/or manage investigator-sponsored research.
You may assist in the review of clinical study protocols and other study documents, contribute to SOP development and/or participate in special projects.
RESPONSIBILITIES:
•Leads or manage components of Phase I, II or III studies
•Assists Biomarker Sciences, Clinical Virology, and/or Clinical Pharmacology in vendor selection and coordinates all interactions and deliverables from vendors.
•May assist as operational contact for Clients studies
•Plans and coordinates all operational activities required with the collection, delivery and analysis of biological samples within a clinical trial
•Manages study timelines, including documentation and communications
•Serves as the point of contact with internal and external stakeholders for successful implementation of all biological sample analysis strategy in Client and Collaborative (CO) programs
•Participates in and manages project meetings and conference calls with CROs, other vendors and cross-functional teams.
•Participates in the functional review of study protocol and other study related documents such as clinical sample management plan, study communication plan, or presentations for Investigator and/or Study Kick-Off meeting.
•Participates in the review and approval of main study and optional informed consents, and may review additional study specific informed consents
•Contributes to SOP development and/or participates in special projects
•Develops tools and processes that optimize project efficiencies and effectiveness.
•Proactively identifies potential operational challenges and collaborates with key stakeholders to provide solutions to ensure study execution remains on track to projected budgets and timelines.
•Ensures own work complies with established practices, policies and processes, and any regulatory or other requirements.
REQUIREMENTS:
We are all different, yet we all use our unique contributions to serve patients. Please see the following for the qualifications and skills we seek for this role.
Minimum Education & Experience
•MA/ MS / PharmD / PhD with 2 + years' relevant clinical or related experience in life sciences.
•BA / BS / RN with 4 +years' relevant clinical or related experience in life sciences.
•Experience in managing the work of external vendors.
•Meets all requirements for Clinical Trial Management Associate (CTMA) grade 25 position with demonstrable proficiency.
Knowledge & Other Requirements
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Email Alert for Clinical Trials Management Associate - III* jobs in San Mateo, CA, United States
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