Senior CRA – Oncology/Rare Disease, East Coast, Remote

Ergomed Group; Boston (MA); On-site; USD 140,000 - 154,000; Full time

Job summary

Ergomed Group is seeking a Senior Clinical Research Associate based on the East Coast (Boston area) to support on-site and remote monitoring activities across phase 2/3 trials in oncology and rare diseases.

You will verify investigator qualifications, train site staff, assist with regulatory submissions, and mentor junior staff while ensuring compliance and data integrity.

This full-time role offers a collaborative global environment where science, quality, and patient safety are the priority.

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
• Communication, collaboration, and problem-solving skills
• Ability to plan, multitask and work in a dynamic team environment

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 verifiesthat the investigator has adequate qualifications,resources, facilities, equipment and staff toconduct the clinical study throughout the study period.
• Trains investigational site staff as necessary
• When applicable, supports preparation of regulatory and / 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

Regulatory understanding

Clinical trial coordination

English proficiency

Travel nationwide

Education

College/University degree in Life Sciences

Job description

Ergomed Group is seeking a Senior Clinical Research Associate based on the East Coast (Boston area) to support on-site and remote monitoring activities across phase 2/3 trials in oncology and rare diseases.

You will verify investigator qualifications, train site staff, assist with regulatory submissions, and mentor junior staff while ensuring compliance and data integrity.

This full-time role offers a collaborative global environment where science, quality, and patient safety are the priority.