JouléNewResearch Coordinator JouléResearch CoordinatorBoston, MA$25–$28 / hourProject Manager and team members with all phases of clinical research, including Trial Initiation, Coordination, Implementation, Maintenance, and Close-out. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America.
JobotNewSr. Oncology Clinical Research Associate JobotSr. Oncology Clinical Research AssociateBoston, MA$120,000–$140,000 / yearInformation collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. Conducts site visits including but not limited to Pre-study visits, initiation visits, interim monitoring visits, close-out visits to ensure compliance with protocols, Sponsor SOPs, ICH/GCP and all applicable regulations.
South Shore HealthRN Clinical Research Nurse / Dana-Farber Cancer Center South Shore HealthRN Clinical Research Nurse / Dana-Farber Cancer CenterWeymouth, MAIn addition, the Research Nurse utilizes evidence-based nursing practice and has expertise in developing and coordinating a plan of care designed to meet the physical, psychological, and social needs of those cancer patients and their families undergoing therapy in a clinical research trial. Participates in Division of Nursing / Institute committees at the main DFCI Longwood campus, including, but not limited to, the monthly Research Nurse Practice Committee meeting.
Hebrew SeniorLifeNewClinical Nurse Coordinator- PT Nights Hebrew SeniorLifeClinical Nurse Coordinator- PT NightsBoston, MA$69,669–$104,503Assume responsibility for intervention in family matters requiring immediate attention, and refer appropriately to Nurse Manager/DON and/or Social Service Department for long-term management and follow-up. Communicate with the Administrative Coordinator and appropriate Nurse Manager/DON on staffing, scheduling, clinical, and administrative issues.
Hebrew SeniorLifeNewClinical Nurse Coordinator Hebrew SeniorLifeClinical Nurse CoordinatorDedham, MA$102,162–$153,244Assume responsibility for intervention in family matters requiring immediate attention, and refer appropriately to Nurse Manager/DON and/or Social Service Department for long-term management and follow-up. Communicate with Administrative Coordinator and appropriate Nurse Manager/DON on staffing, scheduling, clinical and administrative issues.
Boston Children's HospitalNewSenior Program Coordinator Boston Children's HospitalSenior Program CoordinatorBoston, MARemote$55,369.60–$88,576.80Knowledge and skills necessary to solve complex problems in the areas of clinical/research operations, business planning, financial management, marketing, personnel and information systems management. Supporting the Nursing Science Fellowship (basic overview of fellowship below)To provide a structured program of clinical inquiry scholarship and its use in advancing nursing science.
Clinical Dynamix, Inc.NewAssociate Director, Clinical Operations Clinical Dynamix, Inc.Associate Director, Clinical OperationsWatertown, MAWork closely with translational medicine team to ensure appropriate incorporation of bioanalytical sampling plan into clinical protocols and relevant data output of the trial is provided to functional groups for review. Provide study-specific training and leadership to clinical research staff, CRO, CRAs, sites and other contract personnel.
Joslin Diabetes CenterClinical Research Coordinator I (Clinical, Behavioral & Research Outcomes) Joslin Diabetes CenterClinical Research Coordinator I (Clinical, Behavioral & Research Outcomes)Boston, MAFull timeOverview As a member of the clinical research team, the Clinical Research Coordinator's responsibilities will be associated with multiple clinical research projects including dietary intervention studies, pharmaceutical trials, studies evaluating novel diabetes care technologies, with an emphasis on weight management in diabetes. Recruits, schedules, and interviews patients, performs routine laboratory procedures (including measuring blood pressure, height and weight, blood glucose), and escorts patients to testing locations.
Boston Medical CenterClinical Research Coordinator III, Clinical Research Network Boston Medical CenterClinical Research Coordinator III, Clinical Research NetworkBoston, MA$47,500–$66,500 / yearThe 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. Career Advancement/Professional Development: Access a wealth of ongoing training and development opportunities that will not only enhance your skills but also expand your knowledge base especially for individuals pursuing careers in medicine or biomedical research.
Boston Medical CenterClinical Research Coordinator II Boston Medical CenterClinical Research Coordinator IIRoxbury, MAThe CRC II 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, grant supporting document preparation, and participates with the research team and pediatric research services central team in preparation of data and other reports. Under the supervision of the Senior Research Manager and Principal Investigator, the Clinical Research Coordinator II (CRC II) will perform research and research support activities using approved techniques.
Adams ClinicalClinical Research Coordinator I Adams ClinicalClinical Research Coordinator IWatertown, MA$27–$33 / hourSupport investigational product (IP) accountability for assigned studies, including receipt, storage, dispensing, reconciliation, temperature monitoring, and documentation under supervision, ensuring compliance with protocol and site SOPs. Guided by our core values—Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration—we create an environment where meaningful work drives meaningful change.
Brigham and Women's HospitalClinical Research Coordinator Brigham and Women's HospitalClinical Research CoordinatorBoston, MA$20.16–$29.01 / hourConducts library searches • Verifies accuracy of study forms • Updates study forms per protocol • Documents patient visits and procedures • Assists with regulatory binders and QA/QC procedures • Assists with interviewing study subjects • Administers and scores questionnaires • Provides basic explanation of study and in some cases obtains informed consent from subjects • Performs study procedures, which may include phlebotomy • Assists with study regulatory submissions • Writes consent forms • Verifies subject inclusion/exclusion criteria • Performs administrative support duties as required. SKILLS/ABILITIES/COMPETENCIES REQUIRED: • Careful attention to details • Good organizational skills • Ability to follow directions • Good communication skills • Computer literacy • Working knowledge of clinical research protocols • Ability to demonstrate respect and professionalism for subjects' rights and individual needs.
Peregrine TeamClinical Research Coordinator Peregrine TeamClinical Research CoordinatorBoston, MAFull timePeregrine Team is seeking a Clinical Research Coordinator to support clinical trial operations for a leading pharmaceutical organization. Coordinate day-to-day clinical trial activities, including patient scheduling and follow-ups.
Adams ClinicalClinical Research Coordinator II Adams ClinicalClinical Research Coordinator IIBoston, MA$27.19–$37 / hourMaintain investigational product (IP) accountability for assigned studies, including receipt, storage, dispensing, reconciliation, temperature monitoring, documentation, and proper disposal, ensuring compliance with protocol, regulatory requirements, and site SOPs. This role is ideal for coordinators with experience managing one or more trials, supporting day-to-day study operations, and working collaboratively with research staff under guidance from senior team members.
Lahey Hospital and Medical CenterClinical Research Coordinator I, Allergy and Immunology Lahey Hospital and Medical CenterClinical Research Coordinator I, Allergy and ImmunologyBurlington, MA$19.23–$30.77 / hourStart Mode: Car Transit Bike Walk Transit Bus Subway Train Tram Rail Default Fewer transfers Less walking Avoid Tolls Highways Ferries G Google Maps Apple Maps Waze Apple Maps doesn't support Bike mode; we'll open Driving. Similar jobs: Marcantonio Lab Clinical Research Coordinator- March/April Start Date Posted February 11, 2026 Post Doctoral Clinical Research Fellow Posted February 10, 2026 Research Assistant II Posted February 10, 2026.
Lowell General HospitalClinical Research Coordinator - Res G&C - Neely Center for Clinical Cancer Research Lowell General HospitalClinical Research Coordinator - Res G&C - Neely Center for Clinical Cancer ResearchBoston, MA$44,778.55–$55,978.47 / yearResponsible for assisting with Institutional Review Board (IRB) requirements for each study including meeting institutional educational requirements, submitting documents for review such as amendments, adverse event reporting and annual reviews. Individual offers are determined using a comprehensive approach that considers relevant experience, certifications, education, skills, and internal equity to ensure compensation is fair, consistent, and aligned with our business goals.
Joslin Diabetes CenterClinical Research Coordinator I Joslin Diabetes CenterClinical Research Coordinator IBoston, MAFull timeActual compensation is determined based on several factors, that may include seniority, education, training, relevant experience, relevant certifications, geography of work location, job responsibilities, or other applicable factors permissible by law. Ensure that study visits and source documents are completed in accordance with study protocols, including verifying the work of other staff members .
Dana-Farber Cancer Institute IncClinical Research Coordinator - Breast Oncology Dana-Farber Cancer Institute IncClinical Research Coordinator - Breast OncologyBOSTON, MA$48,100–$54,400 / yearOverview The CRC Clinical Research Coordinators work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager. We strive to create an inclusive diverse and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds and design programs to promote public health particularly among high-risk and underserved populations.
Shriners Children'sClinical Research Coordinator II Shriners Children'sClinical Research Coordinator IIBoston, Massachusetts$27.09–$40.63 / hourReporting to the Clinical Research Program Manager (or local Hospital Administrator/Clinic Director) and Research Programs Office at SHC International Headquarters, the CRC provides support in accordance with SHC’s policies and procedures, SHC’s hospital regulations, the Code of Federal Regulation, and Good Clinical Practice guidelines, when applicable. Employees in a FT or PT status (40+ hours per pay period) will also be eligible for paid time off, life insurance, short term and long-term disability and the Flexible Spending Account (FSA) plans and a Health Savings Account (HSA) if a High Deductible Health Plan (HDHP) is elected.
Dana-Farber Cancer Institute IncClinical Research Coordinator- Center for Early Detection and Interception Blood Cancers Dana-Farber Cancer Institute IncClinical Research Coordinator- Center for Early Detection and Interception Blood CancersBOSTON, MA$48,100–$54,400 / yearOverview The CRC Clinical Research Coordinators work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager. Responsible for data entry of study-specific activity, including but not limited to monitor visits, external site enrollment, amendments, receipt of Safety Reports, etc., into Clinical Trial Management System contemporaneously with activity completed.
Boston UniversityFHS CLINICAL RESEARCH COORDINATOR, School of Medicine, Framingham Heart Study Boston UniversityFHS CLINICAL RESEARCH COORDINATOR, School of Medicine, Framingham Heart StudyBoston, MA$34–$55The ideal candidate will value team work, have excellent communication skills and attention to detail. Additionally, it is important that this person be personable/ engage positively with the FHS participants.
Dana-Farber Cancer Institute IncClinical Research Coordinator - Sarcoma Dana-Farber Cancer Institute IncClinical Research Coordinator - SarcomaBOSTON, MA$48,100–$54,400 / yearThe CRC (Clinical Research Coordinators) work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations.
Boston Children's HospitalClinical Research Assistant Boston Children's HospitalClinical Research AssistantBoston, MAThis role involves coordinating research studies, maintaining clinical and research databases, recruiting and enrolling participants, assisting with remote and in-person study visits, collecting and managing study data, and collaborating closely with investigators and multidisciplinary research teams. Assist in developing supportive study documents such as informed consent forms, monitoring templates, study subject tracking tools, monitoring forms, study manuals, and training materials, as required for a study.
Tufts UniversitySenior Research Coordinator - Human Nutrition Research Center on Aging Tufts UniversitySenior Research Coordinator - Human Nutrition Research Center on AgingBoston, MassachusettsThe Senior Research Coordinator works with Principal Investigator and other research staff to coordinate and execute the NIH-funded study entitled: The Impact of Biological Mechanisms of Aging on Response Variability to Resistance Training in Older Adults (BRIO). Overview: The mission of the Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University (HNRCA) is to promote healthy aging through nutrition science to empower people seeking to enjoy long, active, and independent lives.
Tufts UniversityResearch Coordinator - Human Nutrition Research Center on Aging Tufts UniversityResearch Coordinator - Human Nutrition Research Center on AgingBoston, MassachusettsThe goal of this Research Coordinator position is to help coordinate multiple protocols being conducted in the MRU; assist with multiple aspects of the study set up; work with study participants; assist in various study tasks during the active study such as administering questionnaires and collecting outcome measures; and assist with data collection, data management, and quality control checks. Overview: The mission of the Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University (HNRCA) is to promote healthy aging through nutrition science to empower people seeking to enjoy long, active, and independent lives.
Medpace Holdings IncExperienced Clinical Research Associate Hematology/Oncology Medpace Holdings IncExperienced Clinical Research Associate Hematology/OncologyBoston, MAApplicants with experience in any of the below indications will be considered: • Monitoring as a CRA or working as a study coordinator or clinician • Solid Tumor Breast/Ovarian/Prostate/Colorectal/Bladder/Lung/Kidney/Pancreatic Cancer • Small Cell Lung Cancer • Graft vs Host Disease • Glioblastoma • Melanoma • Leukemia • Lymphoma • Mesothelioma. Named a Top Workplace in 2024 by The Cincinnati Enquirer Recognized by Forbes as one of Americas Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
Medpace, Inc.Experienced Clinical Research Associate - Hematology/Oncology Medpace, Inc.Experienced Clinical Research Associate - Hematology/OncologyBoston, MassachusettsCandidates must have at minimum a Bachelor’s degree in a health or science related field, minimum one year of clinical research experience or relevant direct industry experience (e.g., CRC), ability to travel nationwide, must be detail-oriented, strong time management, and communication skills. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.
Boston Medical CenterClinical Research Nurse II, Cancer Boston Medical CenterClinical Research Nurse II, CancerBoston, MA$89,500–$130,000 / yearAs clinically facing research staff, it is expected that the Clinical Research Nurse will spend the majority of their time in clinic seeing active study patients and will be expected to follow and evaluate 4-6 patients per day 4 days/week (16-24 patients per week). Will work with providers to identify potentially eligible patients for open clinical trials, and meet with potential research subjects to review consent forms and discuss trial requirements.
Boston Medical CenterClinical Research Nurse, Pediatrics Boston Medical CenterClinical Research Nurse, PediatricsBoston, MA$34.38–$50 / hourKey responsibilities include maintaining a leadership role in the prenatal, pediatric HIV and research activities of the section of pediatric infectious diseases integrating clinical care, patient education and access to research protocols appropriate for the BMC population. The major responsibilities of this position will be maintaining a leadership role in the prenatal, pediatric HIV and research activities of the section of pediatric infectious diseases integrating clinical care, patient education and access to research protocols appropriate for the BMC population.
Boston Children's HospitalClinical Research Assistant - CAIR and HPNP Boston Children's HospitalClinical Research Assistant - CAIR and HPNPBoston, MAThe Center for Advanced Intestinal Rehabilitation and Home Parenteral Nutrition Program is seeking a Clinical Research Assistant to support day-to-day study operations, participant engagement, clinical data collection and management, and collaboration with our interdisciplinary gastroenterology and surgical research teams. This position will also support two additional industry-sponsored clinical trials:A multicenter study evaluating DEFENCATH in reducing central-line associated bloodstream infections (CLABSIs) in adults receiving total parenteral nutrition through a central venous catheter.
Boston Medical CenterResearch Assistant II - Clinical Research Unit Boston Medical CenterResearch Assistant II - Clinical Research UnitBoston, MAResponsibilities include identifying and screening research subjects, recruiting and maintaining follow-up of research subjects, tracking absent (lost to follow) subjects, explaining and acquiring signatures of subjects for informed consent documents, data collection, database entry (including, but not limited to, data entry, transcription of qualitative questionnaires and coding of qualitative data), and participation in study meetings and performing other administrative tasks in support of the clinical studies. Conducts the screening and/or enrollment of study participants, in both inpatient and outpatient settings, including explaining research procedures, and obtaining informed consent of subjects; as well as interviewing human research subjects for research studies.
Headlands Research IncClinical Research Site Director Headlands Research IncClinical Research Site DirectorPlymouth, MAHighly detail-oriented with exceptional organizational skills Strong critical thinker who can prioritize, problem-solve, and execute under pressure Comfortable managing multiple priorities without losing sight of the big picture Tech-savvy with strong computer and reporting skills Clear, confident communicator with the ability to build trust across teams and external partners Customer- and patient-focused mindset. You will have the autonomy, visibility, and support to implement best-in-class operational processes, mentor and inspire your team, and directly impact enrollment performance, data quality, and financial outcomes.
Propedix, Inc.Clinical Study Coordinator Propedix, Inc.Clinical Study CoordinatorMilford, MA$25–$30 / hourThis role will work closely with internal leadership, investigators, CRO partners, and clinical sites to ensure studies are conducted in compliance with regulatory requirements, Good Clinical Practice (GCP), and study protocols. Our flagship product, featuring our breakthrough anti-fungal and drying agent technology, launched in Q3 2025, and we have a pipeline of advanced OTC and Rx treatments in dermatology and health.
Boston Children's HospitalClinical Research Assistant- Retinal Disease Ophthalmology Boston Children's HospitalClinical Research Assistant- Retinal Disease OphthalmologyBoston, MAThis Clinical Research Assistant will join an established team of clinicians and researchers in Ophthalmology dedicated to understanding blinding pediatric retinal diseases and identifying those patients who may be eligible for treatment trials. Coordinates and prepares the necessary documentation for Institutional Review Board IRB and Committee on Clinical Investigations CCI submissions, in collaboration with other team members and Principal Investigator.
Boston Children's HospitalNewClinical Research Assistant - Yu Lab Boston Children's HospitalClinical Research Assistant - Yu LabBoston, MACommunicating schedule of study events with research families and serve as liaison to the families/patients in the research studies, conducted at both on-site and off-site locations, guiding and advising them throughout each phase of the study. This is an exciting opportunity to work within a multidisciplinary team furthering research and bringing new treatments to rare genetic conditions and is an ideal position for someone who desires to be at the intersection of cutting-edge research and patient care.
CTTX HealthClinical Research Associate CTTX HealthClinical Research AssociateCambridge, MA$103,000–$105,000We’re looking for a Clinical Research Associate (CRA) to join a fast-growing biotech company (confidential) that’s advancing innovative therapies in neuroscience. Collaborate with site staff and cross-functional teams to solve challenges and keep trials on track.
eGenesis IncSenior Clinical Research Associate eGenesis IncSenior Clinical Research AssociateCambridge, MA$105,600–$158,400 / yearIndependently manage assigned investigative sites, including academic medical centers with limited IND experience, providing operational guidance to ensure protocol compliance, data quality, and effective management of high-volume clinical data. Demonstrated experience in independently managing investigative sites and conducting site qualification, initiation, routine monitoring (on-site and remote), and closeout visits, while ensuring compliance with ICH-GCP, regulatory requirements, and study protocols.
Brigham and Women's HospitalClinical Research Associate Brigham and Women's HospitalClinical Research AssociateBoston, MA$20.16–$29.01 / hourThe CRA I will perform the following data management duties under general supervision by the Clinical Research Manager: • Verify adequate documentation of consent, required screening tests and procedures, and eligibility criteria to ensure patients meet all inclusion/exclusion criteria • Enroll patients as required by the study sponsor and internal enrollment monitor team • Follow patients for the duration of study participation via electronic medical record review to ensure protocol compliance • Complete data entry as required for individual study protocols ensuring compliance with institutional and regulatory requirements • Monitor and report adverse events and deviations as required by the sponsor, institution, and federal regulations • Maintain research charts and/or electronic files for all enrolled patients • Ensure adequate source documentation is in place for all data reported • Resolve data queries issued by the sponsor • Obtain protocol clarifications from the study sponsor and communicate information to the research team • Schedule and prepare for monitoring visits with sponsors • Organize and prepare for internal and external audits • Maintain ongoing communication with clinical team regarding study patients and progress for multiple studies. The following regulatory duties may be performed under general supervision by the Clinical Research Manager: • Maintain and organize study specific regulatory binders • Prepare and submit protocol amendments, continuing reviews, and safety reports to the IRB • Revise informed consent documents to include new risk information and/or updated protocol requirements through the course of the study • Manage adverse event and deviation/violation/exception documentation for all enrolled patients and report to the sponsor and IRB as required • Submit Data and Safety Monitoring Reports • Maintain source documentation of correspondence with the IRB, investigators, and sponsors throughout the clinical trial process • Collect, complete, and submit essential regulatory documents to various regulatory entities • Participate in monitoring visits and file all monitoring visit correspondence • Ensure appropriate documentation of delegation and training for all study staff members • Maintain screening and enrollment logs.
University of Massachusetts Medical SchoolClinical Coordinator University of Massachusetts Medical SchoolClinical CoordinatorWestborough, MassachusettsUnder the general direction of the Associate Director, or designee, the Clinical Coordinator is responsible to develop, prioritize, and oversee staff activities specifically designed to promote the coordination of care for those MassHealth members who have medically complex, chronic or catastrophic illnesses that require a customized approach to how, when, and where they receive medically necessary health care services. 3 years of related work experience with prior authorization and/or eligibility determinations for disabled, medically complex, home care, rehab or long term care populations strongly preferred.
Boston Medical CenterResearch Study Coordinator Boston Medical CenterResearch Study CoordinatorBoston, MAUnder the supervision of the Program Manager, the Research Study Coordinator will support the Massachusetts Community Engagement Alliance (MA-CEAL) program, an NIH-funded project focused on promoting COVID-19 vaccine confidence, encouraging diverse participation in clinical research, and addressing health equity issues in our communities. Provide operational and logistical support of ongoing studies, including overseeing participant recruitment, reimbursement, electronic survey deployment, and managing direct communication with study participants.
Alliance for Clinical Trial in Oncology FoundationClinical Research Associate Alliance for Clinical Trial in Oncology FoundationClinical Research AssociateBoston, MA$57,000–$75,000Accurately enter and manage data within the Clinical Trial Management System (CTMS) by: tracking completed training information that could carry over to other studies; maintaining site information and rosters; reviewing monitoring reports to identify deficiencies, reviewing adequacy of issue escalation and issue resolution; and provide feedback to appropriate CRO contacts. This role is responsible for key site management and study start-up activities, including feasibility assessments, site selection support, maintenance of trial master files (eTMF), and oversight of clinical trial systems such as CTMS.
Care AccessDirector, Clinical Research Operations Care AccessDirector, Clinical Research OperationsBoston, MARemote$120,000–$160,000 / yearWith programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Director of Clinical Research Operations provides leadership and oversight for all clinical staff supporting brick-and-mortar research sites, mobile/pop-up sites, and hybrid clinical trial models.
Boston Medical CenterResearch Assistant II Part Time Boston Medical CenterResearch Assistant II Part TimeRoxbury, MADuties 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, and performing other administrative tasks in support of the clinical studies. The RA2 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 supports the research team with the preparation of data and other reports.
Boston Medical CenterResearch Assistant II Boston Medical CenterResearch Assistant IIRoxbury, MADuties include but are not limited to, assisting with patient recruitment, scheduling study visits, consenting study subjects, administering questionnaires, delivering health literacy curriculum materials directly to study subjects, creating and filing case report forms, entering and updating data, maintaining databases, running reports, and performing other administrative tasks in support of the clinical studies. The Telehealth Epilepsy Care Collaborative (TECC) is recruiting a full-time Research Assistant II (RA2) to assist in the implementation of a project designed to improve mental health literacy, reduce stigma and foster resiliency in children and youth with epilepsy with comorbid mental illness served at Boston Medical Center (BMC).
Harvard UniversityResearch Associate Giannobile Lab Harvard UniversityResearch Associate Giannobile LabCambridge, MA$65,000–$90,000 / yearAdditionally, experience coordinating clinical research projects is preferable as the role may include project management responsibilities such as the development and oversight of study protocols, managing regulatory submissions, facilitating IRB communications, tracking project milestones and budgets, and supporting training and data collection activities at multiple study sites. The ideal candidate will demonstrate proficiency in conducting supervised research, possess strong communication skills, be self-motivated, maintain a high degree of integrity, and demonstrate a willingness and ability to acquire new technical skills.
Boston Medical CenterResearch Assistant Boston Medical CenterResearch AssistantBoston, MADuties include but are not limited to, assisting with patient recruitment, scheduling study visits, administering questionnaires and conducting qualitative interviews, creating and filing case report forms, entering and updating data, maintaining databases, running reports, and performing other administrative tasks in support of the research studies. Performs office-related duties such as answering phones, picking up and delivering mail, ordering and distributing office supplies, handling faxes, scanning, filing, photocopying, collating materials, maintaining the update of policy manuals, etc.
Boston Medical CenterProgram Manager Infectious Diseases Research Boston Medical CenterProgram Manager Infectious Diseases ResearchBoston, MAKey responsibilities include working with the study team to develop protocols and assessment instruments; monitoring study implementation and data quality at study sites; mentoring/co-supervising study team; preparing/assisting in the development of manuscripts/presentations; and ensuring compliance with reporting to grant funding institutes and the IRB. The Program Manager is responsible for planning and managing the overall execution of research initiatives by the PI, including meeting necessary quality, budget, and timeline targets, and making or recommending operational strategies and/or decisions (with input from study team and PI) in support of achieving research objectives.
Brigham and Women's HospitalPACO Research Program/Project Manager Brigham and Women's HospitalPACO Research Program/Project ManagerBoston, MA$63,648–$90,750.40 / yearExperience 3+ years experience in an academic, research, or related setting required Experience in international settings is required Program Management Work independently under the general direction of the research faculty members Partner with the faculty members to develop and optimize scientific group strategy and management Provide technical oversight and supervision of research assistant that work on projects within their managed portfolio Work with recruiting team to recruit a new research assistant cohort within the MPEC each year, and facilitate recruitment efforts at international sites by participating in job description development, posting employment opening advertisements in setting-appropriate channels, screening applicants, and interviewing selected candidates Meet regularly with programmatic leadership to discuss strategic planning, opportunities to enhance operations, and management approaches Ensure research integrity, including data documentation and data management, by developing best practices, provide ongoing training, and monitoring for adherence Monitor personnel resource allocations and advise MPEC leadership on factors affecting research productivity Manage and participate in collaborative grant-writing projects Keep team aware of research conferences and associated deadlines Research Project Management Coordinate all administrative aspects of multiple active and pending projects At project outset, clarify project goals, deliverables, tasks, timeline, and research team Throughout project duration, plan, track, and report on project tasks, responsible parties, timelines, etc. Ensure research quality by closely monitoring adherence to research protocols and data/materials agreements for each project in management portfolio Serve as a liaison between team members at various US and international collaborative research sites Manage study project coordinators in areas of financial documentation, reporting, procurement, and maintenance of study equipment and supplies Monitor employment contracts of international staff and engage with local HR offices to address contract issues including pay changes, promotions, and renewals In conjunction with the Compliance Manager, coordinate and monitor Institutional Review Board applications and reporting for international projects, including all applicable review dates and deadlines to prevent lapses in approval In conjunection with the Compliance Manager, coordinate data sharing/materials transfer agreements and manage data and materials exchanges among collaborating institutions Additional Job Details (if applicable) Remote Type Onsite Work Location 100 Cambridge Street Scheduled Weekly Hours 40 Employee Type Regular Work Shift Day (United States of America) Pay Range $63,648.00 - $90,750.40/Annual
RetinAI MedicalClinical Site Support Specialist RetinAI MedicalClinical Site Support SpecialistBoston, MAThis person will be responsible for building relationships with a clinical site’s research coordinators and PI’s, performing a medical record review of pre-identified patients to evaluate clinical trial eligibility based on a sponsor’s protocol, delivering the results to the sites, and monitoring and collecting the outcomes. This role will work closely with our data science and research team to ensure quality and accuracy of client deliverables as well as serving as an SME for consulting on eligibility criteria when needed.
CRISPR Therapeutics AGClinical Scientist/ Senior Clinical Scientist CRISPR Therapeutics AGClinical Scientist/ Senior Clinical ScientistSouth Boston, MA$125,000–$140,000 / yearSince its inception over a decade ago, CRISPR Therapeutics has transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, cardiovascular and rare diseases. Familiarity with ICH, GCP, and relevant regulatory requirements, and strong analytical and strategic thinking skills, experience with interacting with medical monitors, development operations (preclinical, clinical operations, regulatory affairs, Quality Assurance) and clinical investigators.