Clinical Research Coordinator II, Clinical Research Network

Boston Medical Center’s Clinical Research Network (CRN) provides a centralized community engaged, equity support structure for BMC’s research community. Our mission is to pursue and share world class scientific discovery and innovation through the conduct of community-engaged clinical research that is responsive to cultural and linguistic differences and inclusive of all people. The CRN also provides focused clinical research staffing infrastructure to strategically important and under-resourced trials at BMC. The Clinical Research Network Clinical Research Coordinator II (CRC II) position provides clinical research support for studies managed by Boston Medical Center’s Clinical Research Network (CRN), under the direction of the CRN Manager, and affiliated Principal Investigators. The CRC II will coordinate CRN supported research protocols in the clinic setting within hospital policy and procedures, protocol compliance and regulatory guidelines consistently and independently. The CRC II will coordinate assigned administrative aspects of each assigned study and interact with study subjects, CRN Program Manager, CRN Community Engagement & Recruitment Specialist, study investigators, ancillary departments, and other research and clinical staff. Duties include but are not limited to, assisting with patient recruitment, eligibility screening, consenting, scheduling study visits, administering questionnaires (as applicable), collecting, entering and updating data, maintaining databases and participant documentation, running reports, and performing other administrative and research tasks in support of the clinical study. In addition to study management, the CRC II may be asked to support community engagement efforts at local community and hospital-based events. The CRC II maintains contact with sponsors to ensure complete and timely data collection, maintains patient study folders, assists with documenting financial and budgetary needs of CRN studies, and supporting the research team with the preparation of data and other reports.

Position: Clinical Research Coordinator II, Clinical Research Network

Location: Boston, MA

Schedule: 40 hours per week

ABOUT BMC:

At Boston Medical Center (BMC), our diverse staff works together for one goal — to provide exceptional and equitable care to improve the health of the people of Boston. Our bold vision to transform health care is powered by our respect for our patients and our commitment to ensure everyone who comes through our doors has a positive experience.

You’ll find a supportive work environment at BMC, with rich opportunities throughout your career for training, development, and growth and where you’ll have the tools you need to take charge of your own practice environment.  

POSITION SUMMARY:

The Clinical Research Coordinator II (CRC II) procures, processes and ships research specimens and conducts patient recruitment, administers questionnaires, abstracts medical records, maintains patient databases, enters data into sponsor-specific electronic data capture forms, performs administrative tasks, assists in grant preparation, and participates with the research team in preparation of data and other reports. Will also assist with audits, quality improvement projects, and CRN directed community engagement efforts

ESSENTIAL RESPONSIBILITIES / DUTIES:

• Evaluating and tracking the eligibility of all patients seen in the clinic, EMR reports, or community engagement events

• Obtaining informed consent and registering patients to cohort studies and other protocols. Reviewing and abstracting the medical records for patients, including review of pathology reports.

• Entering information into the appropriate EMR and eCRF systems and departmental systems in an accurate manner.

• Reviewing data for quality and completeness based on established queries.

• Assists with the coordination of the collection, processing, organization, and storage of biological specimens in the systems

• May be responsible for IRB and regulatory submissions and maintenance of regulatory files

• Maintaining on-going communications with research managers and PIs for data collection needs.

(The above statements in this job description are intended to depict the general nature and level of work assigned to the employee(s) in this job.  The above is not intended to represent an exhaustive list of accountable duties and responsibilities required).

JOB REQUIREMENTS

EDUCATION/EXPERIENCE:

• Baccalaureate Degree Required

• Master’s Degree preferred OR

• 2-5 years experience

• Special Intermittent Project Responsibilitie