- Dana-Farber Cancer Institute (Boston, MA)
- The Clinical Research Coordinator will support the Breast Oncology Cohort Studies Program and its clinical and translational research in the areas of screening, ... may also screen patients for protocol eligibility, obtain informed consent, and register study participants to cohort and banking studies . **We are considering… more
- Actalent (Natick, MA)
- Job Title: Study Coordinator (9 month contract) Job Description The Study Coordinator will engage in human subject research, monitoring participants ... using various technology products and collecting data throughout the study sessions. The role involves consenting participants, taking necessary vitals and… more
- Actalent (Natick, MA)
- Study Coordinator Job Description We are seeking a Study Coordinator to conduct human subject research. The role involves monitoring participants using ... ensuring the proper functioning of devices and data collection throughout the study sessions. Responsibilities + Consent participants according to protocol and take… more
- Actalent (Natick, MA)
- …ensuring the proper functioning of devices and data collection throughout the study sessions. Great opportunity to gain experience in clinical research! Schedule: + ... ensure proper data collection. + Guide participants through the study and support data collection directly. Required Skills +...data entry. + Ability to direct participants through the study , with examples of patient care or people interaction.… more
- Beth Israel Lahey Health (Burlington, MA)
- …varying degrees of complexity with moderate oversight. + Implements assigned research studies by reviewing study and assessing protocol and institutional ... coordinator /sponsor relationship. + Completes start-up checklists and implements study start-up plan, including source worksheet creation. + Prepares, completes… more
- Dana-Farber Cancer Institute (Boston, MA)
- A position is immediately available for a Neuropathology Clinical Research Coordinator to join the Precision Medicine Program within the DFCI Department of ... goals of this position are to facilitate human research studies which depend on tissue and blood specimens from...report forms, adverse events reporting, filing and archiving of study records, and resolution of data queries. + Participate… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …and coordination of assigned study monitoring and auditing visits with study coordinator , Investigator, DF/HCC ODQ, Industry Sponsors, and third party ... Center for RAS Therapeutics is looking for a Regulatory Coordinator (RC) to provide regulatory support for this new...and submits regulatory documents, and maintains records on assigned studies to ensure regulatory compliance with DFCI and DF/HCC… more
- Dana-Farber Cancer Institute (Boston, MA)
- …the quality of life for all of those affected by cancer. The Clinical Research Coordinator II (CRC II) will be an integral part of the clinical research program and ... protocol eligibility, and obtaining consent from patients for industry-sponsored and biobanking studies . In this way, the CRC II will be responsible for collecting,… more
- Dana-Farber Cancer Institute (Boston, MA)
- …and coordination of assigned study monitoring and auditing visits with study coordinator , Investigator, DF/HCC QACT, Industry Sponsors, and third party ... submissions, prepares and submits regulatory documents, and maintains records on assigned studies to ensure regulatory compliance with DFCI and DF/HCC policies as… more
- Dana-Farber Cancer Institute (Boston, MA)
- …Early Detection and Interception of Blood Cancers seeks a **Clinical Research Coordinator ** to assist in the day-to-day management of non-interventional trials. This ... responsible for the data collection and management of the non-interventional studies . The CRC will maintain timely communication with participants, collaborating… more
- Beth Israel Lahey Health (Boston, MA)
- … studies ), respond to IRB comments on applications submitted and work with study team in getting studies activated for enrollment of patients. + Prepare ... for the projects conducted by the BIDMC Clinical Research Coordinator Core The Clinical Research Coordinator Core...consent form changes, continuing reviews, violations and deviations to study protocols. + Oversees reporting of AEs, SAEs, IND… more
- Dana-Farber Cancer Institute (Boston, MA)
- …Cancer Institute Division of Population Sciences is currently seeking a Clinical Research Coordinator I to work on cancer research projects that focus on adult ... patient populations. The Clinical Research Coordinator 's efforts will primarily be focused on enrolling and...efforts will primarily be focused on enrolling and tracking study participants, administering survey to study participants,… more
- Tufts Medicine (Lowell, MA)
- …will assist the Principal Investigator (PI) in planning and implementing clinical research studies as assigned. This individual will play a key role in expanding ... professional who can navigate the challenges of implementing and conducting clinical studies with minimal on-site supervision. The CRC III will be responsible for… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible ... also screen patients for protocol eligibility, obtain informed consent, and register study participants to clinical trials. . Some travel may be required. Located… more
- Dana-Farber Cancer Institute (Boston, MA)
- …Research Program at Dana-Farber Cancer Institute is seeking a Clinical Research Coordinator (CRC) to join our program. The GI Oncology Clinical Research Program ... esophageal, stomach, liver, pancreas, colon, and neuroendocrine. The Clinical Research Coordinator works within the GI Oncology clinical research program and… more
- Beth Israel Lahey Health (Boston, MA)
- …people's lives.** This position will support the operations and conduct of clinical research studies at BIDMC as part of the BIDMC Clinical Research Coordinator ... Core. Projects supported cross therapeutic areas and research study types. Position may work in the main hospital setting or affiliated community locations. The … more
- Tufts Medicine (Boston, MA)
- …Principal Investigator (PI) in planning and implementing clinical research studies as assigned. **Job Description** **Minimum Qualifications** **:** 1. Bachelor's ... may be assigned. 1. Assists in the recruitment of study participants. 2. Completes follow up with study... study participants. 2. Completes follow up with study participants in prescribed settings as required. 3. Completes… more
- Tufts Medicine (Boston, MA)
- …the Principal Investigator (PI) in planning and implementing clinical research studies as assigned. **Principal Duties And Essential Functions:** * Responsible for ... assisting in the recruitment of study participants. Assesses potential patients and eligibility for inclusion...patients to obtain information for eligibility assessment, explain the study , and obtains signature for the informed consent form.… more
- Tufts Medicine (Boston, MA)
- …Center is seeking a highly motivated and detail-oriented Research Administrative Coordinator to join the Clinical and Translational Research Center (CTRC). The ... will be responsible for providing critical support across multiple research studies . This includes assisting with protocol review, budget creation and submission,… more
- Kelly Services (Waltham, MA)
- **Principal Clinical Trial Coordinator ** Kelly(R) Science & Clinical is hiring a contract Principal Clinical Trial Coordinator for one of our global CRO clients. ... and technical support to the Project Team as a study lead, acting as a cross functional liaison. Coordinates...line manager as appropriate. + Supports the maintenance of study specific documentation and global support with specific systems,… more