Clinical Research Coordinator II

McLean Hospital; Belmont (MA); On-site; USD 33,000 - 49,000; Full time

Job summary

McLean Hospital in Belmont, MA is seeking a dedicated clinical research support professional. Working independently under general supervision, you will assist in screening potential trial participants, support recruitment strategies, and help manage study datasets.

You will collaborate with the Principal Investigator, train new staff, and may supervise in a smaller area. A Bachelor's degree and 1–2 years of related experience are required, with strong data literacy and communication skills.

Qualifications

• Bachelor's degree required; experience may not substitute the degree.
• Must have at least 1 year of directly related clinical research experience.
• High computer literacy and knowledge of data management programs.
• Ability to work independently with excellent communication and detail-oriented skills.
• Strong knowledge of clinical research protocols and data interpretation.

Responsibilities

• Coordinate implementation of sponsored clinical studies internally and externally.
• Screen applicants for eligibility and assess suitability for participation.
• Develop and implement patient recruitment strategies with the PI.
• Develop, organize, and maintain the study database with quality control.
• Assist with literature reviews and preparation for publications.
• Train and orient new staff; may supervise in smaller areas.
• Support data analyses with the lab's statistical consultant when needed.
• Ensure compliance with IRB approval and protocol changes.

Skills

Data management

Independence

Interpersonal skills

Communication skills

Analytical skills

Clinical research protocols

Organizational skills

Attention to detail

Respect for subjects' rights

Education

Bachelor's degree

Tools

MS Office

Data management software

Job description

McLean Hospital in Belmont, MA is seeking a dedicated clinical research support professional. Working independently under general supervision, you will assist in screening potential trial participants, support recruitment strategies, and help manage study datasets.

You will collaborate with the Principal Investigator, train new staff, and may supervise in a smaller area. A Bachelor's degree and 1–2 years of related experience are required, with strong data literacy and communication skills.