Senior Clinical Research Associate - Oncology/ Rare Disease

ERGOMED; Boston (MA); Hybrid; USD 90,000 - 130,000; Full time

Job summary

Ergomed is seeking a Clinical Monitor to perform on-site or remote monitoring across Pre-Study, Initiation, Interim and Close-Out visits to ensure sites are qualified and prepared for trials. You will train site staff, support regulatory submissions, and mentor junior staff, with strong English, life sciences background, and willingness to travel nationally.

Join Ergomed to contribute to safe and effective clinical research across oncology and rare disease programs, collaborating with global

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

Life Sciences degree

English proficiency

Travel nationally

Multitasking

Team collaboration

Communication skills

Education

College/University degree in Life Sciences

Job description

Ergomed is seeking a Clinical Monitor to perform on-site or remote monitoring across Pre-Study, Initiation, Interim and Close-Out visits to ensure sites are qualified and prepared for trials. You will train site staff, support regulatory submissions, and mentor junior staff, with strong English, life sciences background, and willingness to travel nationally.

Join Ergomed to contribute to safe and effective clinical research across oncology and rare disease programs, collaborating with global