Senior Clinical Research Associate

Remote Jobs; United States; Remote; USD 75,000 - 95,000; Full time

Job summary

A leading clinical research company in the United States is seeking an experienced on-site monitor to manage study activities and site communication. The ideal candidate has over 5 years of experience in oncology trials and a strong background in life sciences. This position offers flexible work options, including home-based opportunities, in a collaborative environment.

Qualifications

• Minimum of 5 years of independent on-site monitoring experience.
• Experience in Phase II and/or III oncology studies.
• Full working proficiency in English.

Responsibilities

• Conduct and report onsite monitoring visits.
• Manage site communication and study timelines.
• Support regulatory documentation preparation.

Skills

On-site monitoring experience

Knowledge of oncology trials

Proficiency in English

Communication skills

MS Office applications

Education

College/University degree in Life Sciences

Job description

Employer Industry: Clinical Research

Why consider this job opportunity

• Opportunity to advance your career in clinical research with a dynamic global company
• Engage in challenging full-service projects on a country/regional level
• Hands-on involvement in every aspect of the study
• Work in a supportive and collaborative environment that prioritizes its people
• Flexible work options: office-based or home-based positions available

What to Expect (Job Responsibilities)

• Conduct and report all types of onsite monitoring visits
• Manage site communication and oversee study activities, timelines, and schedules
• Perform CRF review, source document verification, and query resolution
• Support the regulatory team in preparing documents for study submissions
• Participate in quality control, including compliance monitoring and report reviews

What is Required (Qualifications)

• College/University degree in Life Sciences or an equivalent combination of education, training, and experience
• Minimum of 5 years of independent on-site monitoring experience in the USA
• Experience in all types of monitoring visits for Phase II and/or III studies
• Proven experience monitoring complex Oncology trials, specifically breast cancer
• Full working proficiency in English and proficiency in MS Office applications

How to Stand Out (Preferred Qualifications)

• Demonstrated ability to plan, multitask, and work in a dynamic team environment
• Strong communication, collaboration, and problem-solving skills
• Valid driver's license (if applicable)

#ClinicalResearch #CareerAdvancement #OncologyTrials #DynamicWorkEnvironment #RemoteWorkOptions

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