Clinical Research Coordinator II, Neurology

BMC Software•Boston, MA

5d•Onsite

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. The Department of Neurology is seeking a Clinical Research Coordinator (CRC) II for multiple projects in clinical research and clinical trials. Under the supervision of the Principal Investigators and with some leadership by the Associate Director and Project Manager for assigned research studies, the Clinical Research Coordinator (CRC) will perform research activities using approved techniques. The CRC will manage tasks related to clinical trials: recruitment, data management, and regulatory management. Will also assist with audits and quality assurance reviews; and prepares and attends site visits.

Requirements

CRC II: Experienced Level Position
Master’s Degree OR Bachelor’s Degree plus 2-5 years of experience
Special Intermittent Project Responsibilities (2-5 per year)
Excellent organization and communications skills required
Strong interpersonal skills; ability to effectively interact with all levels of staff and externals contacts
Cultural sensitivity and comfort with a wide range of social, racial and ethnic populations
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

Nice To Haves

Bilingual in Spanish preferred
REDCap knowledge strongly preferred
Phlebotomy skills a plus

Responsibilities

Evaluating and tracking the eligibility of all patients seen in the clinic.
Recruits subjects to participate in the assigned study by using approved methodologies, such as, reaching to healthcare providers for referrals, visiting clinics, using approved advertisements.
Conducts the enrollment of study participants, including explaining research procedures, and obtaining informed consent of subject and registering patients to cohort studies and other protocols.
Schedules appointments of study participants; conducts reminder phone calls and/or sends mail-outs.
Performs biospecimen collection for study purposes, including but not limited to: blood (phlebotomy), saliva (cheek swabs), urine collection.
Performs office-related duties such as answering phones, picking up and delivering mail, storing and distributing office supplies, handling faxes, scanning, filing, photocopying, collating materials, maintaining the update of policy manuals, etc.
Reviews and abstracts the medical records for patients, including review of all records for inclusion/exclusion criteria.
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.
Supervises and trains student research assistants in EMR data abstraction and data entry.
Reviewing data for quality and completeness for each enrollee for completion and quality (QA).
Answers queries; performs data collection entry into database; maintains clear, concise, accurate and legible records.
Assists with the coordination of the collection, processing, organization, and storage of biological specimens in the systems
May assist in the preparation for IRB and regulatory submissions and maintenance of regulatory files