Clinical Research Coordinator 1

Mass General Brigham; Boston (MA); On-site; USD 50,000 - 75,000; Full time

Job summary

A leading healthcare institution in Boston seeks a Clinical Research Coordinator I to manage various research studies under the supervision of a principal investigator. This role requires a Bachelor's degree and prior clinical research experience, focusing on studies related to neurological outcomes and sleep disorders. The coordinator will engage in both administrative and operational support, assisting with participant recruitment, regulatory compliance, and data management. This position provides an opportunity to contribute to groundbreaking research in a collaborative environment.

Qualifications

• Bachelor's degree required.
• Prior experience in clinical research preferred.
• CITI Certification can be completed upon hire.

Responsibilities

• Coordinate research studies, ensuring compliance with regulations.
• Assist with data collection and participant scheduling.
• Prepare study reports and maintain study documentation.

Skills

Attention to detail

Communication skills

Analytical skills

Organizational skills

Education

Bachelor's Degree

Job description

Site: The General Hospital Corporation

Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.

Job Summary

The CRC I will work under the general supervision of Dr. Aleksandar Videnovic at the MGH Neurological Clinical Research Institute (NCRI). The coordinator will act as the primary coordinator for one to two research studies performed at the NCRI. Dr. Videnovic’s research is centered on how sleep affects neurological outcomes and includes several clinical research projects in Parkinson’s Disease (PD) and REM Sleep Behavior Disorder (RBD). Current projects include studies investigating biomarker discovery for synuclein-specific neurodegenerative disorders such as Parkinson’s disease, projects centered on the sleep-wake cycles and circadian rhythms in PD and RBD, applications of light therapy aimed at improving sleep and fatigue in patients with PD for as well as several clinical research studies dedicated to neuroimaging and novel therapeutic drugs and devices. These studies require both individual and team efforts to complete. Dr. Videnovic frequently works with internal staff members and at other institutions, both inside and outside of Boston, in coordinating multi-center trials.

Qualifications

PRINCIPAL DUTIES AND RESPONSIBILITIES:

Administrative

• Provide support to the Principal Investigator (PI, Aleksandar Videnovic, MD MSc), co-investigators, and all other study collaborators
• Ensure regulatory requirements are met in accordance with GCP (Good Clinical Practice) and HIPAA (Protection of Human Research Subjects) standards
• Assist in the maintenance of all study regulatory documents, including the preparation of annual IRB submissions, any needed IRB modifications, correspondence with the study sponsors, and the physical regulatory binder
• Verify the accuracy of study forms
• Regularly inform the PI and study team of progress towards recruitment targets and milestones
• Assist the Principal Investigator in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials
• Perform other related duties as required (e.g., data entry, data checking/cleaning, literature reviews)
• Prepare data for analysis and data entry
• Work with PI to prepare and complete study reports

Operational:

• Provide a basic explanation of study details and, in some cases, obtain informed consent from subjects
• Assist in the administration of clinical assessments of the study subjects, including but not limited to screening, evaluation, and administration of online assessments to participants, and coordination of biospecimen collection
• Assist with the setup of sleep studies, actigraphy, and pupillometry
• Communicate frequently with MGH employees and sponsor representatives to ensure study visits are conducted appropriately
• Abstract medical records
• Contact participants regarding scheduling and data collection
• Assist with data collection, processing, entry, storage, and quality control for clinical research studies
• Coordinate study intervention sessions
• Participate in subject recruitment and assist with determining the suitability of research subjects
• Assist with developing and implementing recruitment strategies

Complete study visits that require EKG, phlebotomy, and vital signs collection

SKILLS AND COMPETENCIES REQUIRED:

• Ability to work well independently as well as with co-workers, peers, supervisors, and patients
• Careful attention to detail and accuracy
• Ability to manage multiple tasks & priorities, and set deadlines
• Computer literacy
• Working knowledge of clinical research protocols
• Analytical skills and the ability to resolve technical problems
• Excellent communication and interpersonal skills
• Strong organizational and data management skills

EDUCATIONAL REQUIREMENTS:

Bachelor's Degree

EXPERIENCE:

CITI Certification may be completed upon hire

Prior experience working in a clinical research setting preferred

Additional Job Details (if applicable)

Physical Requirements

• Standing Frequently (34-66%)
• Walking Frequently (34-66%)
• Sitting Occasionally (3-33%)
• Lifting Frequently (34-66%) 35lbs+ (w/assisted device)
• Carrying Frequently (34-66%) 20lbs - 35lbs
• Pushing Occasionally (3-33%)
• Pulling Occasionally (3-33%)
• Climbing Rarely (Less than 2%)
• Balancing Frequently (34-66%)
• Stooping Occasionally (3-33%)
• Kneeling Occasionally (3-33%)
• Crouching Occasionally (3-33%)
• Crawling Rarely (Less than 2%)
• Reaching Frequently (34-66%)
• Gross Manipulation (Handling) Frequently (34-66%)
• Fine Manipulation (Fingering) Frequently (34-66%)
• Feeling Constantly (67-100%)
• Foot Use Rarely (Less than 2%)
• Vision - Far Constantly (67-100%)
• Vision - Near Constantly (67-100%)
• Talking Constantly (67-100%)
• Hearing Constantly (67-100%)

Remote Type

Onsite

Work Location

165 Cambridge Street

Scheduled Weekly Hours

40

Employee Type

Regular

Work Shift

Day (United States of America)

EEO Statement:

The General Hospital Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran’s Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at (857)-282-7642. Mass General Brigham Competency Framework

At Mass General Brigham, our competency framework defines what effective leadership “looks like” by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.