Clinical Research Coordinator II - Boston Medical Center
Boston, MA 02118
About the Job
POSITION SUMMARY:
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.
The CRCII will participate in multiple clinical studies as approved by the grant(s) in the areas of substance use disorder in pregnancy. The CRCII will oversee the administrative aspects of the grant and interact with study subjects, clinical research coordinators, study investigators, work study students and other research staff. Duties include but are not limited to, assisting with patient recruitment, scheduling study visits, administering questionnaires, creating and filing case report forms, entering and updating data, maintaining databases, running reports, collection of biological samples (blood, hair, saliva, placenta, urine), storing samples, and performing other administrative tasks in support of the clinical studies. The CRCII maintains contact with the participating sites to insure complete and timely data collection, maintains patient profiles, assists with documenting financial and budgetary needs of the grant, and supporting the research team with the preparation of data and other reports.
Position: Clinical Research Coordinator II
Department: Pediatrics
Schedule: Full Time
Requirements
Qualifications
Req id: 23755
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.
The CRCII will participate in multiple clinical studies as approved by the grant(s) in the areas of substance use disorder in pregnancy. The CRCII will oversee the administrative aspects of the grant and interact with study subjects, clinical research coordinators, study investigators, work study students and other research staff. Duties include but are not limited to, assisting with patient recruitment, scheduling study visits, administering questionnaires, creating and filing case report forms, entering and updating data, maintaining databases, running reports, collection of biological samples (blood, hair, saliva, placenta, urine), storing samples, and performing other administrative tasks in support of the clinical studies. The CRCII maintains contact with the participating sites to insure complete and timely data collection, maintains patient profiles, assists with documenting financial and budgetary needs of the grant, and supporting the research team with the preparation of data and other reports.
Position: Clinical Research Coordinator II
Department: Pediatrics
Schedule: Full Time
Requirements
- 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.
Qualifications
- 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
- CRC II: Experienced Level Position
- Baccalaureate Degree Required at time of hire
- 2-5 years experience preferred
- Special Intermittent Project Responsibilities (2-5/year)
Req id: 23755
Source : Boston Medical Center