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Mass General Brigham
Charlestown, MA, United States
Please note, the functions below are representative of major duties that are typically associated with these positions. Specific responsibilities may vary based upon departmental needs. Similarly, not all duties that have been outlined will be assign Clinical Research, Research Coordinator, Clinical, Coordinator, Research, Healthcare, Patient
Job Source: Mass General BrighamMassachusetts General Hospital
Boston, MA, United States
GENERAL SUMMARY/OVERVIEW STATEMENT: The Clinical Research Coordinator (CRC) is an integral member of an interdisciplinary research team, which supports the clinical studies in the Neuroendocrine Unit (Department of Medicine) that are focused on the endocrine regulation of eating behavior and metabolism in eating disorders and obesity. Under the su
Job Source: Massachusetts General HospitalMassachusetts General Physicians’ Organization
Boston, MA, United States
Job Description - Clinical Research Coordinator I (3285644) Clinical Research Coordinator I - ( 3285644 ) Under supervision of the Director of the MGH Ataxia Center, Dr. Jeremy Schmahmann, and working in collaboration with a multidisciplinary team, the incumbent will be responsible for supporting all aspects of clinical research coordination fo
Job Source: Massachusetts General Physicians’ OrganizationShriners Children's
Boston, MA, United States
Company Overview: Shriners Childrens is an organization that respects, supports, and values each other. We are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global impact. We foster a learning environment that values evidenced based practice, experience, innovation, and critical thinking
Job Source: Shriners Children'sShriners Children's
Boston, MA, United States
Company Overview: Shriners Childrens is an organization that respects, supports, and values each other. We are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global impact. We foster a learning environment that values evidenced based practice, experience, innovation, and critical thinking.
Job Source: Shriners Children'sChildren's Hospital Boston
Boston, MA, United States
76082BRJob Posting Title:Clinical Research CoordinatorDepartment:Computational Health Informatics ProgramAutoReqId:76082BRStatus:Full-TimeStandard Hours per Week:40 Job Posting Category:ResearchJob Posting Description: We are seeking a Research Coordinator to join PrecisionLink, a major research initiative at Boston Childrens Hospital. The aim of t
Job Source: Children's Hospital BostonBeth Israel Lahey Health
Boston, MA, United States
**Job Type:** Regular **Time Type:** Full time **Work Shift:** Day (United States of America) **FLSA Status:** Non-Exempt **When you join the growing BILH team, you're not just taking a job, youre making a difference in peoples lives.** The Innovation in Cancer (ICan) Program is a vibrant and fast-growing multi-disciplinary team conducting Early Dr
Job Source: Beth Israel Lahey HealthAlcanza Clinical Research
Roslindale
Job Description Job Description Description Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in Boston and Northern MA, Portsmouth, NH, Charleston, SC, Charlotteville, VA, and Detroit, MI. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccin
Job Source: Alcanza Clinical ResearchBoston, MA, United States
Overview:
The Clinical Research Coordinator I s responsibilities may be associated with one or more clinical research project(s). The Coordinator works directly with pediatric patients and their families, and is responsible for coordinating assigned study/studies.
As a health care organization, we have the responsibility to do everything in our power to care for and protect our patients, our colleagues and our communities. We require that all staff be vaccinated against influenza (flu) and COVID-19 as a condition of employment.
Responsibilities:
In all activities, adhere to Good Clinical Practice guidelines and maintain patient confidentiality per HIPAA regulations
Identify potentially eligible participants using appropriate data sources
Assess eligibility of potential study participants
Become familiar with relevant content of all relevant study protocols
Communicate clinical trial updates to other team members
Describe studies to potential participants, explain rationale for and details of participation
Obtain informed consent and assent, when appropriate
Schedule study visits and prepare relevant materials for each visit (tubes, paperwork, etc.)
Arrange participant travel, as applicable
Collect primary data from study participants and their guardians
After completing training, measure vital signs and perform other relevant procedures and tests
Ensure that study visits and source documents are completed in accordance with study protocols, including verifying the work of other staff members
Enter data into electronic data capture forms and respond to queries
Process laboratory samples and ship to central laboratories
Ensure timely reporting of abnormal findings to investigator and participants
Document and communicate all serious adverse events and other safety reports to the study team and investigator
Maintain up-to-date inventory of study supplies and place orders
Modify study documents, such as informed consent form and recruitment materials, when needed
Prepare documents for submission to IRBmay include initial protocol submissions, protocol amendments, annual continuing review, etc.
Maintain all regulatory and subject binders in audit-ready condition
Correspond with study sponsors, contract research organizations, and other collaborators, as applicable
Assist with study start-up and close-out activities, as relevant
Participate in study teleconferences, attend team meetings, and attend national meetings and/or investigator meetings, as relevant (may involve travel)
Participate in occasional off-site recruitment events (requires some schedule flexibility)
Other duties as assigned.
Qualifications:
Bachelors degree (in a relevant field of study preferred)
1-2 years of relevant post-graduate experience preferred
Fluency in written and spoken English
Spoken Spanish preferred
Basic knowledge of Microsoft Office Suite and ability to navigate at a basic level within various web-based applications.
Graphic design/layout skills (to design brochures, flyers, etc.) desirable
Ability to follow general instructions and procedures, as provided.
Strong interpersonal, organizational and communication skills (communicate clearly and effectively via verbal and written instruction).
Meticulous attention to detail
Professional and warm in demeanor, especially when relating to study participants and their families
Ability to maintain confidentiality
Ability to prioritize responsibilities through completion.
Ability to work independently and with others in the team - to interact respectfully with other employees, professional staff and/or external contacts.
Excellent critical thinking and problem-solving abilities
Ability to learn sophisticated concepts and detailed protocols quickly
Ability to work with minimal oversight, after training period
Ability to manage administrative complexity arising from multiple concurrent studies
Flexible schedule as necessary to accommodate study patients and recruitment activities
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Email Alert for Clinical Research Coordinator I jobs in Boston, MA, United States
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