Clinical Research Coordinator 1

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.

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. Videnovics research is centered on how sleep affects neurological outcomes and includes several clinical research projects in Parkinsons Disease (PD) and REM Sleep Behavior Disorder (RBD). Current projects include studies investigating biomarker discovery for synuclein-specific neurodegenerative disorders such as Parkinsons 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 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.

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 accuracy of study forms
Regularly inform 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 & 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 ability to resolve technical problems.
Excellent communication and interpersonal skills.
Strong organizational and data management skills.

Job Summary

Summary
Following established policies procedures and study protocols provides assistance on clinical research studies including recruiting evaluating and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy EKGs etc.; and maintaining and updating data generated by the study. Candidates who are in the process of completing their bachelors degree have a six-month grace period from their hire date (up to one year if starting on a per diem basis)to provide degree equivalency verification.

Does this position require Patient Care
No

Essential Functions
-Reviews proposals for compliance with sponsor and organizational guidelines; verifies that all sponsor requirements are met.

-Recruiting patients for clinical trials and conducting phone interviews.

-Verifies the accuracy of study forms and updates them per protocol.

-Prepares data for analysis and data entry.

-Documents patient visits and procedures.

-Assists with regulatory binders and QA/QC Procedures.

-Assists with interviewing study subjects.

-Assists with study regulator submissions.

Education
Bachelors Degree Related Field of Study required

Can this role accept experience in lieu of a degree
Yes

Licenses and Credentials

Experience
Some relevant research project work 0-1 year preferred

Knowledge Skills and Abilities
- Careful attention to detail and good organizational skills.
- Ability to follow directions.
- Good interpersonal and communication skills.
- Computer literacy.
- Working knowledge of clinical research protocols.
- Ability to demonstrate respect and professionalism for subjects rights and individual needs.

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%)

Onsite

165 Cambridge Street

40

Regular

Day (United States of America)

Pay Range

$20.16 - $29.01/Hourly

Grade

5

At Mass General Brigham we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive and any offer extended will take into account your skills relevant experience if applicable education certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however it does not encompass all elements contributing to your total compensation addition to competitive base pay we offer comprehensive benefits career advancement opportunities differentials premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply and our Talent Acquisition team will provide an overview of your potential compensation and benefits package.

1200 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 Veterans 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 .

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