Clinical Research Associate II

Remote Jobs; United States; Remote; USD 70,000 - 90,000; Full time

Job summary

A leading placement agency is seeking a Clinical Research Monitor with a College degree in Life Sciences and at least 2 years of independent monitoring experience. Responsibilities include acting as a liaison between project teams and sites, ensuring compliance, and conducting training. The role offers the chance to work on diverse studies, with opportunities for travel and skill development in a collaborative environment.

Qualifications

• Minimum of 2+ years of independent on-site monitoring experience.
• Experience in all types of monitoring visits, in phases I-III.
• Experience in GI preferred.

Responsibilities

• Act as the main line of communication between the project team, sponsor, and site.
• Prepare, conduct, and report site selection, initiation, routine monitoring, and close-out visits.
• Ensure timely definition and communication of subject recruitment targets.

Skills

Independent on-site monitoring

Experience in Oncology

Full working proficiency in English

Strong planning

Multitasking

Team collaboration

Education

College/University degree in Life Sciences

Tools

MS Office

Job description

Why consider this job opportunity

• Opportunity for career advancement and growth within the organization
• Chance to work on diverse clinical studies across various therapeutic indications
• Supportive and collaborative work environment
• Great opportunity to further develop skills and expertise in clinical research
• Ability to travel up to 75%, providing exposure to different sites and experiences

What to Expect (Job Responsibilities)

• Act as the main line of communication between the project team, sponsor, and site
• Prepare, conduct, and report site selection, initiation, routine monitoring, and close-out visits
• Ensure timely definition and communication of subject recruitment targets and project timelines at the site level
• Perform source data verification and manage study risks at the site level
• Conduct project-specific training of site investigators

What is Required (Qualifications)

• College/University degree in Life Sciences or an equivalent combination of education, training, and experience
• Minimum of 2+ years of independent on-site monitoring experience
• Experience in all types of monitoring visits, in phases I-III
• Experience in Oncology mandatory; experience in GI preferred
• Full working proficiency in English and proficiency in MS Office applications

How to Stand Out (Preferred Qualifications)

• Located in Central or West Coast preferred
• Experience in radio-pharm preferred
• Strong planning, multitasking, and team collaboration skills
• Valid driver's license (if applicable)

#ClinicalResearch #ContractResearchOrganization #CareerOpportunity #Oncology #MonitoringExperience

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