Clinical Research Coordinator II, General Internal Medicine (Gout Study, part time)
About The Position
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 Under the supervision of the Lead CRC, Senior Research Manager and Principal Investigator for assigned research studies, the Clinical Research Coordinator (CRC) II will perform research activities using approved techniques. The CRC 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 and quality improvement projects.
Requirements
- CRC II: Experienced Level Position
- Baccalaureate Degree Required
- OR 2-5 years experience
- Excellent organization and communications skills required.
- Strong interpersonal skills; ability to effectively interact with all levels of staff and externals contacts.
- Must be detail oriented and have the ability to follow-through.
- Ability to effectively manage time and prioritize workload.
- Must practice discretion and adhere to hospital confidentiality guidelines at all times.
- Must have computer skills including the use of Microsoft Office Suite
- The CRC II will work exclusively on the TRUST trial (Treat-to-Target Serum Urate versus Treat-to-Avoid Symptoms in Gout) which test two different treatment strategies for managing gout.
- This is a hybrid, position (20-26 hours/week).
- A minimum 2-year commitment is strongly preferred.
- Flexibility to work some evening hours as needed.
Nice To Haves
- Master’s Degree preferred
Responsibilities
- Evaluating and tracking the eligibility of all patients seen in the clinic.
- Obtaining informed consent (for non-treatment studies) and registering patients to cohort studies and other protocols.
- Reviewing and abstracting the medical records for patients, including review of pathology reports.
- Accessing patient demographic and clinical information from the clinical systems.
- 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.
Benefits
- Competitive pay
- Tuition reimbursement and tuition remission programs
- Highly subsidized medical, dental, and vision insurance options
- Career Advancement/Professional Development: Access a wealth of ongoing training and development opportunities that will not only enhance your skills but also expand your knowledge base especially for individuals pursuing careers in medicine or biomedical research.
- Pioneering Research: Engage in groundbreaking research projects that are driving the forefront of biomedical science.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Part-time
Career Level
Mid Level
Number of Employees
1,001-5,000 employees
