Senior CRA (West Coast)
San Diego, United States · Remote · Full-time
- Posted 4d ago
- From Sitero LLC’s careers page
- Location
- San Diego, United States
- Work mode
- Remote
- Type
- Full-time
- Level
- Senior
- Experience
- 3+ years
- Department
- Other
Opens the listing on sitero.bamboohr.com
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About the role
Job Title:
Senior CRA (West Coast)
Location:
Remote
Function:
Clinical Operations
ESSENTIAL DUTIES AND RESPONSIBILITIES:
- Primary point of contact for site personnel during life cycle of clinical trial. This includes study start up support, site activation, trial conduct and closeout of a clinical trial.
- Provides support to the Global Project Lead and CTM during project start up to ensure timely site selection and feasibility. Assists with collection of essential documents from the site. May assist with submission of central EC Applications, Local EC applications, RA applications and any other local regulatory applications/Approvals required.
- Ability to identify protocol deviations and pharmacovigilance issues that might affect data accuracy or patient safety.
- Conduct Site qualification, site initiation, routine site monitoring close out visits (remote and onsite), Central monitoring in compliance with study protocol and ICH-GCP.
- Expert documentation of monitoring priorities/activities via site visit confirmation and follow up letters, monitoring visit reports, and any trial associated logs.
- Oversees conduct trials by reviewing study data listings, vendor dashboards, and CTMS issues/actions documentation to identify trends, errors, and any potential breeches that can impact data integrity.
- Ability to present essential function of CRA role in Bid Defenses, Investigator Meetings, and Sponsor Face to Face meetings.
- Assists the Global Project Lead in identification of out-of-scope activities.
- Basic understanding of assigned projects scope, milestones and budget and manages site level activities to ensure project deliverables are met.
- Provides support to the CTM and Global project lead in negotiation of site budgets and contracts.
EDUCATION AND EXPERIENCE REQUIRED:
- Bachelors degree
- 5 Years of experience with a CRO with 3 years independent drug trial monitoring experience
COMPENSATION & BENEFITS:
Sitero proudly offers an impressive compensation package and benefits, including a competitive salary, paid time off, and healthcare and retirement benefits.
EMPLOYMENT TYPE:
Full Time, Permanent
COMMITMENTS:
- Standard Hours 40 hours per week, one hour lunch, Monday – Friday. Additional hours as needed.
- Willing to work in shifts as and when needed.
- Up to 80% travel for Days on Site visits
DISCLAIMER:
Sitero is an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.
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About Sitero LLC
Clinical research services and eClinical technologySitero is a contract research organization offering clinical operations, site support, data management, biostatistics, medical writing, and eClinical technology.
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