Senior Clinical Research Associate

Sunnyvale, CA, US • Posted 7 hours ago • Updated 7 hours ago

Contract W2

Contract Corp To Corp

On-site

Depends on Experience

Fitment

Dice Job Match Score™

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Job Details

Skills

Auditing
Clinical Research
Clinical Trial Management System
Clinical Trials
Collaboration
Communication

Summary

We are looking for Senior Clinical Research Associate for our client in Sunnyvale, CA

Job Title: Senior Clinical Research Associate

Job Location: Sunnyvale, CA

Job Type: Contract

Job Overview:

Pay Range: $87hr - $92hr

Support end to end clinical research activities to ensure successful study start up and execution through regulatory approval.
Manage and track clinical study data, site performance, and study progress.
Assist in investigator selection, training, and patient recruitment activities.
Support site start up and activation including preparation of study documentation and monitoring plans.
Work with clinical systems including EDC, CTMS, eTMF, and imaging platforms.
Review regulatory submissions, consent forms, and documentation to ensure compliance.
Assist in updating clinical study documents including protocols, CRFs, and monitoring plans.
Conduct site visits including qualification, initiation, monitoring, and close out activities.
Perform source data verification to ensure accuracy and compliance.
Support clinical trial sites with data entry, query resolution, and study oversight.
Collaborate with data management teams to support data cleaning and validation.
Maintain clinical documentation and reporting including study files and status reports.
Assist in audit preparation and support during internal and external audits.
Support investigator meetings, site training, and study presentations.

Requirements/Must Have:

Strong experience in clinical research and clinical trial management.
Knowledge of Good Clinical Practice and regulatory requirements.
Experience with clinical trial systems such as EDC, CTMS, and eTMF.
Experience in protocol development, informed consent, and regulatory documentation.
Ability to manage multiple priorities and work in cross functional teams.
Strong communication and stakeholder management skills.
Ability to travel as required.

Experience:

Minimum 8 plus years of clinical research experience with a bachelor s degree or equivalent.
Minimum 6 plus years of experience with advanced degree in nursing or related field.
Minimum 5 plus years of experience with advanced degrees such as master s, MD, or PhD.

Responsibilities:

Coordinate and manage clinical trial activities across sites.
Ensure compliance with protocols and regulatory requirements.
Conduct monitoring visits and validate study data.
Support study planning, execution, and reporting.
Assist in audit preparation and regulatory inspections.
Collaborate with stakeholders to ensure successful study delivery.

Skills:

Clinical research and trial management.
Regulatory compliance and Google Cloud Platform knowledge.
Data management and validation.
Communication and stakeholder coordination.
Problem solving and organizational skills.

Qualification And Education:

Bachelor s degree in a related field required.
Advanced degree such as Nursing, Master s, MD, or PhD is preferred.
Certification in clinical research or trial management is preferred.
Knowledge of statistics and clinical study design is preferred.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 10516350
Position Id: CA_SCRA_0319
Posted 7 hours ago

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