Senior Clinical Research Associate - East Coast (Remote/On‑Site)

Ergomed Group; Raleigh (NC); On-site; USD 90,000 - 120,000; Full time

Job summary

Ergomed Group seeks a Senior Clinical Research Associate based on the East Coast to conduct on-site and remote monitoring activities for phase 2/3 trials, primarily in oncology or rare diseases. The role involves training staff, mentoring, and supporting regulatory submissions.

You will collaborate across sites, ensure compliance, and travel nationally to monitor study sites. English proficiency is required, with a flexible approach to on-site and remote work.

Qualifications

• College/University degree in Life Sciences or an equivalent combination of education, training & experience.
• Extensive on-site monitoring experience in phase 2/3 trials, ideally with experience of complex trials in oncology or rare disease.
• Full working proficiency in English.
• Ability to travel nationally.

Responsibilities

• Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study.
• Identifies the investigators and verifies that the investigator has adequate qualifications, resources, facilities, equipment and staff to conduct the clinical study throughout the study period.
• Trains investigational site staff as necessary
• When applicable, supports preparation of regulatory and / or EC submissions
• Participates in mentoring/training of new staff as well as performing co-monitoring visits, to assess junior staff performance.

Skills

On-site monitoring

Remote monitoring

Study coordination

English proficiency

Education

Life Sciences degree

Job description

Ergomed Group seeks a Senior Clinical Research Associate based on the East Coast to conduct on-site and remote monitoring activities for phase 2/3 trials, primarily in oncology or rare diseases. The role involves training staff, mentoring, and supporting regulatory submissions.

You will collaborate across sites, ensure compliance, and travel nationally to monitor study sites. English proficiency is required, with a flexible approach to on-site and remote work.