Clinical Research Coordinator II – Oncology & Biospecimens

BMC Software; Boston (MA); On-site; USD 43,000 - 60,000; Full time

Benefits offered by this job

Competitive pay

Tuition reimbursement

Tuition remission

Medical, dental, vision insurance

Career advancement/professional dev

Pioneering research

Job summary

Boston Medical Center is seeking a Clinical Research Coordinator II in the Hematology and Oncology Research division. The role supports translational cancer studies, including biospecimen handling, data abstraction from medical records, and consent for studies and biobank enrollment.

You will work with clinicians and investigators to ensure compliance with IRB requirements and contribute to manuscript preparation.

Qualifications

• Master’s Degree or higher in a relevant field.
• Bachelor’s Degree with 2–5 years of clinical research experience.
• Intermittent project responsibilities (2–5 per year).
• Experience in clinical research, patient recruitment, and biospecimen handling preferred.
• EMR and data management experience beneficial.

Responsibilities

• Recruit, screen, and obtain informed consent for studies and biobank participation.
• Process, label, store, and ship biospecimens per protocol.
• Maintain databases and regulatory documentation.
• Coordinate study activities with clinical and research teams.
• Assist with literature reviews, data summaries, and report/manuscript preparation.
• Perform basic data analysis and prepare figures/tables.
• Operate, maintain, and troubleshoot laboratory equipment and monitor inventory.
• Ensure compliance with regulatory, privacy, and confidentiality requirements.

Skills

MS Office

EMR experience

REDCap

Organizational skills

Communication skills

Multitasking

Independent work

Data management

Education

Master’s Degree

Bachelor’s Degree + 2-5 years experience

Special Intermittent Project Responsibilities

Tools

SOPs

Laboratory equipment

Job description

Boston Medical Center is seeking a Clinical Research Coordinator II in the Hematology and Oncology Research division. The role supports translational cancer studies, including biospecimen handling, data abstraction from medical records, and consent for studies and biobank enrollment.

You will work with clinicians and investigators to ensure compliance with IRB requirements and contribute to manuscript preparation.