Translational Oncology CRC II: Biospecimens, Data & Impact

Boston Medical Center; Boston (MA); On-site; USD 43,000 - 60,000; Full time

Benefits offered by this job

Competitive pay

Tuition reimbursement

Excellent benefits

Job summary

Boston Medical Center is seeking a Clinical Research Coordinator II to support the Translational Research Laboratory and Biospecimen Repository within the Section of Hematology & Medical Oncology. You will obtain informed consent, manage databases, and assist with biospecimen processing, data summaries, and manuscript preparation.

You will work closely with clinicians and researchers, ensure IRB compliance, and contribute to translational studies with opportunities for co-authorship on abstracts

Qualifications

• Master’s Degree or Bachelor’s Degree with 2–5 years of clinical research experience.
• Experience in patient recruitment and biospecimen handling preferred.

Responsibilities

• Recruit, screen, and obtain informed consent for research studies and biobank participation.
• Process, label, store, and ship biospecimens per protocol.
• Maintain accurate databases, research records, 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; coordinate servicing and monitor inventory.
• Ensure compliance with regulatory, privacy, and confidentiality requirements.

Skills

Microsoft Office

EMR experience

REDCap

Data management

Communication skills

Independent work

Education

Masters Degree

Bachelors Degree + 2-5 years experience

Tools

EMR systems

REDCap

Job description

Boston Medical Center is seeking a Clinical Research Coordinator II to support the Translational Research Laboratory and Biospecimen Repository within the Section of Hematology & Medical Oncology. You will obtain informed consent, manage databases, and assist with biospecimen processing, data summaries, and manuscript preparation.

You will work closely with clinicians and researchers, ensure IRB compliance, and contribute to translational studies with opportunities for co-authorship on abstracts