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 HealthNewRN Clinical Research Nurse / Dana-Farber Cancer Center South Shore HealthRN Clinical Research Nurse / Dana-Farber Cancer CenterQuincy, 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.
Takeda PharmaceuticalNewAssociate Medical Director, Clinical Science, NS TAU Takeda PharmaceuticalAssociate Medical Director, Clinical Science, NS TAUCambridge, MA$198,500–$311,850 / yearProvides leadership in meetings and negotiations with key opinion leaders, establishment of strategy for assigned compounds, and the direction of clinical scientists involved in developing documents required to outline the Company positions on research programs or regulatory applications (e.g. Contributes to the development and negotiation of clinical development plans for potential alliances and or in-licensing opportunities, interacts with upper management of potential partner/acquisition companies during DD visits and alliance negotiations and represents clinical science on internal assessment teams.
Takeda PharmaceuticalNewAssociate Director, Quantitative Clinical Pharmacology (QCP) Lead Takeda PharmaceuticalAssociate Director, Quantitative Clinical Pharmacology (QCP) LeadBoston, MA$154,400–$242,550 / yearAdvanced knowledge of pharmaceutical industry, overall drug development process with expertise in the cross-functional interfaces with key partners such as Pharmacometrics, Statistics, Drug Safety, Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/Device, and Global Regulatory Affairs. These scientists (from quantitative clinical pharmacology, statistics, programming, outcomes research and epidemiology, patient safety & pharmacovigilance, digital strategy, library sciences and data architecture/governance) bring their expertise to our global program teams and reimagine our disciplines.
Tufts MedicineNewEpilepsy, Epileptologist - New England Neurological Associates, Nashua, NH Tufts MedicineEpilepsy, Epileptologist - New England Neurological Associates, Nashua, NHLowell, MACollaboration: NENA provides patient care to over 70,000 patients throughout the Merrimack Valley, and through our partnership with Tufts Medicine, we will continue to expand access to healthcare including plans to build a neuro-immunology program and development of a Memory Care Center. Integrated Healthcare: NENA has a collaborative group of 28 Physicians and Advanced Practice Clinicians is part of the Tufts Medicine Health System with over 700 affiliated doctors and a clinical affiliation with Tufts Medical Center.
Tufts MedicineNewOphthalmology, Assistant or Associate Professor, Comprehensive Ophthalmologist Tufts MedicineOphthalmology, Assistant or Associate Professor, Comprehensive OphthalmologistBoston, MAThis historic city is known for its outstanding academic institutions, excellent public and private schools, miles of coastal and island beaches, proximity to New Hampshire and Vermont mountains for skiing and outdoor activities, local arts and cultural attractions including the Boston Symphony, Museum of Fine Arts, and professional sporting teams with the Boston Red Sox, Celtics, Bruins, New England Patriots and Revolution. We facilitate over 90,000 ambulatory care visits a year and perform over 8,000 surgeries a year, providing diagnosis and treatment in all subspecialties of Ophthalmology including cataracts, corneal disorders, refractive disorders, glaucoma, oculofacial plastic and orbital disorders, and vitreoretinal disorders.
Tufts MedicineNewEpileptologist - New England Neurological Associates - Nashua, NH Tufts MedicineEpileptologist - New England Neurological Associates - Nashua, NHNashua, NHCollaboration: NENA provides patient care to over 70,000 patients throughout the Merrimack Valley, and through our partnership with Tufts Medicine, we will continue to expand access to healthcare including plans to build a neuro-immunology program and development of a Memory Care Center. Comprised of Tufts Medical Center, Lowell General Hospital, MelroseWakefield Hospital, Lawrence Memorial Hospital of Medford, Care at Home - an expansive home care network, and large integrated physician network.
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.
Alira HealthClinical Research Associate Alira HealthClinical Research AssociateBoston, MassachusettsThe CRA works closely with Lead CRAs, Sr CRAs, Clinical Trial Coordinators, Director of Clinical Monitoring and Project Managers to ensure protocol compliance, address site questions, and assist with study recruitment, site training, and other site-related issues. Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work, Alira Health SOPs and regulatory requirements, i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) Guidelines.
Brigham and Women's HospitalNewClinical 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. The Clinical Research Associate I (CRA I) works under general supervision to enroll eligible patients to clinical research protocols and manage data collection and regulatory submissions for multiple cancer studies.
Ardelyx IncIn House Clinical Research Associate Ardelyx IncIn House Clinical Research AssociateWaltham, MA$99,000–$121,000 / yearPartner with Clinical Trial Managers and CRO monitoring teams to provide sponsor oversight and ensure monitoring activities align with the study's risk-based monitoring strategy. Building on prior experience in a Clinical Trial Assistant (CTA) or similar role, the CRA II independently manages assigned sites and supports study oversight of clinical trial execution.
ICON PlcSenior Clinical Research Associate ICON PlcSenior Clinical Research AssociateCambridge, MARemoteFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Zp Group LlcOncology Clinical Research Associate Zp Group LlcOncology Clinical Research AssociateBoston, MA$110,000–$135,000 / yearResponsibilities for the Oncology Clinical Research Associate: • Conduct site and study visits and perform all site monitoring activities across multiple study • Responsible for both remote and on-site monitoring and study activation • Participate in the development of study tools, protocols, and clinical trial documentation • Some travel required once travel bands are lifted. Qualifications for the Oncology Clinical Research Associate: • 3+ years of Oncology on-site Monitoring and hands on experience with EDC Systems • Experience with Phase 1 Oncology is non-negotiable • Organization to perform monitoring duties across multiple sites is a must.
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.
Alira HealthIn-House Clinical Research Associate-2 Alira HealthIn-House Clinical Research Associate-2Boston, MassachusettsIn-house CRAs work closely with field CRAs and Clinical Project Managers to ensure the integrity of the trial data without the need for frequent travel. Ensures all regulatory documents are collected and filed appropriately at both the site and in the Trial Master File (TMF); conducts routine file reviews.
Alira HealthIn House Clinical Research Associate Alira HealthIn House Clinical Research AssociateBoston, MassachusettsIn-house CRAs work closely with field CRAs and Clinical Project Managers to ensure the integrity of the trial data without the need for frequent travel. Ensures all regulatory documents are collected and filed appropriately at both the site and in the Trial Master File (TMF); conducts routine file reviews.
Getinge ABSr. Clinical Research Associate Getinge ABSr. Clinical Research AssociateBoston, MAWith a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The Senior Clinical Research Associate will report to the VP Scientific and Medical Affairs and will play an important role in study data management and overall clinical operations of the prospective randomized studies.
Parexel International CorpSenior Clinical Research Associate - Oncology - US - FSP Parexel International CorpSenior Clinical Research Associate - Oncology - US - FSPMAWork in partnership with and/or escalate to the SCP to ensure quality of site deliveryInterface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sitesPartner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risksAttend investigator meeting when required (virtual or F2F). CRA is responsible for the resolution of all protocol-related issues for assigned investigator sites and will work closely with the Site Care Partner (SCP), and other members of the study team, as required, in activities associated with the set-up, running and close-out of sites in a clinical trial.
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.
Alkermes PlcAssociate Director, Clinical Research Scientist (Neurology) Alkermes PlcAssociate Director, Clinical Research Scientist (Neurology)Waltham, MAIn 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts' Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.
Boston Medical CenterClinical Research Coordinator III, Clinical Research Network Boston Medical CenterClinical Research Coordinator III, Clinical Research NetworkBoston, MA$47,500–$66,500 / yearThe CRC procures, processes and ships research specimens and conducts patient recruitment, administers questionnaires, abstracts medical records, maintains patient databases, enters data into sponsor-specific electronic data capture forms, performs administrative tasks, assists in grant preparation, and participates with the research team in preparation of data and other reports. Career Advancement/Professional Development: Access a wealth of ongoing training and development opportunities that will not only enhance your skills but also expand your knowledge base especially for individuals pursuing careers in medicine or biomedical research.
IQVIA Holdings IncSr. Clinical Research Associate, IQVIA IQVIA Holdings IncSr. Clinical Research Associate, IQVIABoston, MADeprecated: preg_replace(): Passing null to parameter #3 ($subject) of type array|string is deprecated in C:\api\public\classes\StringCleaner.class.php on line 85.
Monte Rosa Therapeutics, IncResearch Associate, Translational and Clinical Biomarkers Monte Rosa Therapeutics, IncResearch Associate, Translational and Clinical BiomarkersBoston, MassachusettsHe/she will work in close collaboration with translational/biomarker, project and clinical teams to develop and implement internal and external biomarker activities and perform studies to support indication/patient selection opportunities. The individual in this role will be responsible for designing and executing robust translational experiments in clinically relevant models to support indication selection and patient stratification.
Lahey Hospital and Medical CenterClinical Research Coordinator - BIDMC Clinical Research Coordinator Pool Lahey Hospital and Medical CenterClinical Research Coordinator - BIDMC Clinical Research Coordinator PoolBoston, MA$21.63–$31.25 / yearThis position is embedded within the BIDMC Clinical Research Coordinator Core, a centralized resource serving investigators across departments and divisions throughout the medical center, and operates in affiliation with the institutions Clinical Research Center, a member of Harvard Catalyst - Harvards Clinical and Translational Science Center. Customer Service: Ability to provide a high level of customer service to patients, visitors, staff and external customers in a professional, service-oriented, respectful manner using skills in active listening and problem solving.
Monte Rosa Therapeutics IncResearch Associate, Translational and Clinical Biomarkers Monte Rosa Therapeutics IncResearch Associate, Translational and Clinical BiomarkersBoston, MAHe/she will work in close collaboration with translational/biomarker, project and clinical teams to develop and implement internal and external biomarker activities and perform studies to support indication/patient selection opportunities. The individual in this role will be responsible for designing and executing robust translational experiments in clinically relevant models to support indication selection and patient stratification.
OraClinical Research Coordinator I OraClinical Research Coordinator IAndover, MassachusettsPerform various tasks (post-onboarding) such as use of proprietary technology, performing the Informed Consent process, documenting medical history and medications, taking vitals, scribing for medical staff, dispensing study drug, performing allergy skin tests, documenting controlled environment stats, and other ophthalmic assessments. Our CRC I’s will partner with tenured Clinical Research Coordinators and Clinical Project Managers to execute protocol directives and work cross-functionally with internal and external teams such as other Research Coordinators and Investigators.
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.
Lahey Hospital and Medical CenterClinical Research Coordinator - Stephenson Clinical Research Lahey Hospital and Medical CenterClinical Research Coordinator - Stephenson Clinical ResearchBoston, MA$19.23–$28.37 / 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. Customer Service: Ability to provide a high level of customer service to patients, visitors, staff and external customers in a professional, service-oriented, respectful manner using skills in active listening and problem solving.
Mass General BrighamNewClinical Research Coordinator Mass General BrighamClinical Research CoordinatorBoston, MassachusettsSKILLS/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 The Clinical Research Coordinator II should also possess: - Ability to work independently and as a team player - Analytical skills and ability to resolve technical problems - Ability to interpret acceptability of data results - Working knowledge of data management program. - Conducts 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.
Lahey Hospital and Medical CenterClinical Research Coordinator- Orthopedics Lahey Hospital and Medical CenterClinical Research Coordinator- OrthopedicsBoston, MA$19.23–$28.37 / hourActual 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. Compensation may exceed the base hourly rate depending on shift differentials, call pay, premium pay, overtime pay, and other additional pay practices, as applicable to the position and in accordance with the law.
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.
Brigham and Women's HospitalHome Base Clinical Research Coordinator I Brigham and Women's HospitalHome Base Clinical Research Coordinator ICharlestown, MA$20.16–$29.01 / hourFollowing 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. The Clinical Research Coordinator will support a variety of clinical research studies focusing on treatment for the invisible wounds of war, including evidence-based treatments for PTSD and TBI, mindfulness and wellness-focused modalities, military family care programming, community provider education, etc.
Ora IncClinical Research Coordinator I Ora IncClinical Research Coordinator IAndover, MAPerform various tasks (post-onboarding) such as use of proprietary technology, performing the Informed Consent process, documenting medical history and medications, taking vitals, scribing for medical staff, dispensing study drug, performing allergy skin tests, documenting controlled environment stats, and other ophthalmic assessments. Our CRC I's will partner with tenured Clinical Research Coordinators and Clinical Project Managers to execute protocol directives and work cross-functionally with internal and external teams such as other Research Coordinators and Investigators.
Brigham and Women's HospitalSenior Clinical Research Coordinator - OUD Genomics Brigham and Women's HospitalSenior Clinical Research Coordinator - OUD GenomicsSomerville, MAWorking independently and 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. 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.
Lahey Hospital and Medical CenterClinical Research Coordinator (Electrophysiology & Digital Health Section) Lahey Hospital and Medical CenterClinical Research Coordinator (Electrophysiology & Digital Health Section)Boston, MA$19.23–$28.37 / hourThe variety of tasks associated with this position, include, but are not limited to the following: assisting with study administrative tasks such as, IRB communications and document development, site management and startup activities, writing progress reports, scientific writing (including drafting manuscripts, abstracts, posters, and PowerPoint presentations), grant applications, medical chart review, completion of case report forms, data extraction and upload, site staff communication and patient contact for research studies, and maintain the section's OpenScholar website. Smith Center for Outcomes Research, Electrophysiology & Digital Health Section at BIDMC is seeking a highly motivated Clinical Research Coordinator to be responsible for the managing/overseeing of recruiting, screening and enrolling of patients for participation in a multiple clinical trial, ensuring compliance with federal, state and institutional guidelines.
Brigham and Women's HospitalClinical Research Coordinator I Brigham and Women's HospitalClinical Research Coordinator IBoston, MA$20.16–$29.01 / hourFollowing 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. As a member of the integrative Anesthesia Research Center the CRC, working closely in collaboration with other research coordinators, will be responsible for managing recruitment of patients in multiple clinical trials, participating in data collection and entry, as well as ensuring compliance with federal, state and institutional guidelines.
Beth Israel Lahey HealthClinical Research Coordinator (Electrophysiology & Digital Health Section) Beth Israel Lahey HealthClinical Research Coordinator (Electrophysiology & Digital Health Section)Boston, MassachusettsThe variety of tasks associated with this position, include, but are not limited to the following: assisting with study administrative tasks such as, IRB communications and document development, site management and startup activities, writing progress reports, scientific writing (including drafting manuscripts, abstracts, posters, and PowerPoint presentations), grant applications, medical chart review, completion of case report forms, data extraction and upload, site staff communication and patient contact for research studies, and maintain the section’s OpenScholar website. Smith Center for Outcomes Research, Electrophysiology & Digital Health Section at BIDMC is seeking a highly motivated Clinical Research Coordinator to be responsible for the managing/overseeing of recruiting, screening and enrolling of patients for participation in a multiple clinical trial, ensuring compliance with federal, state and institutional guidelines.
Mass General BrighamNewClinical Research Coordinator I Mass General BrighamClinical Research Coordinator IBoston, MassachusettsFollowing 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. The Center provides a range of clinical services to women which include: consultation regarding the use of psychiatric medications during pregnancy; treatment for postpartum mood and anxiety disorders; treatment for premenstrual syndrome; and treatment of menopause related mood and anxiety symptoms, sleep disorders, and hot flashes.
Joslin Diabetes CenterClinical Research Coordinator I Joslin Diabetes CenterClinical Research Coordinator IBoston, MAActual 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 - GU Oncology Dana-Farber Cancer Institute IncClinical Research Coordinator - GU OncologyBoston, 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.
Dana-Farber Cancer Institute IncNewClinical Research Coordinator - Multiple Myeloma Dana-Farber Cancer Institute IncClinical Research Coordinator - Multiple MyelomaBOSTON, MA$48,100–$54,400 / yearThe CRC (Clinical Research Coordinators) work within the Multiple Myeloma 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.
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.
Dana-Farber Cancer Institute IncClinical Research Coordinator - Immune Effector Cell Therapy Program Dana-Farber Cancer Institute IncClinical Research Coordinator - Immune Effector Cell Therapy ProgramBROOKLINE, MA$48,100–$54,400 / yearThe CRC (Clinical Research Coordinator) will work within the Immune Effector Cell Therapy 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.
Dana-Farber Cancer Institute IncClinical Research Coordinator - Waldenstrom's Macroglobulinemia Dana-Farber Cancer Institute IncClinical Research Coordinator - Waldenstrom's MacroglobulinemiaBOSTON, 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.
Dana-Farber Cancer Institute IncClinical Research Coordinator - Center for Head and Neck Oncology Dana-Farber Cancer Institute IncClinical Research Coordinator - Center for Head and Neck OncologyBoston, MA$48,100–$54,400 / yearThe CRC (Clinical Research Coordinators) work within the Head & Neck Oncology 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.
Brigham and Women's HospitalSenior Clinical Research Coordinator, Dept, of Urology Brigham and Women's HospitalSenior Clinical Research Coordinator, Dept, of UrologyBoston, MA$50,502.40–$82,014.40 / yearThe 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. Works very independently under minimal supervision to enroll eligible patients in clinical research protocols and manage all aspects of data collection and submission for multiple cancer studies.
Mass General BrighamSenior Clinical Research Coordinator, Dept, of Urology Mass General BrighamSenior Clinical Research Coordinator, Dept, of UrologyBoston, MassachusettsThe 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. Works very independently under minimal supervision to enroll eligible patients in clinical research protocols and manage all aspects of data collection and submission for multiple cancer studies.
Boston Children's HospitalNewClinical Research Coordinator - Neurophysiology Research Core (CNRC) Boston Children's HospitalClinical Research Coordinator - Neurophysiology Research Core (CNRC)Boston, MAThrough this collaborative and comprehensive approach, we aim to advance our current scientific understanding and translate what we learn into earlier identification, improved therapies, and better outcomes for children and families affected by neurodevelopmental disorders. The responsibilities of the position will include data collection among participants with diverse neurodevelopmental conditions, EEG and related equipment set-up and maintenance, study protocol development, data uploading and organization, and other relevant data collection tasks.
Brigham and Women's HospitalClinical Research Coordinator I (SPARC-XP Study ) Brigham and Women's HospitalClinical Research Coordinator I (SPARC-XP Study )Boston, MA$20.16–$29.01 / hourAdditional Job Details (if applicable) Remote Type Hybrid Work Location 185 Cambridge Street Scheduled Weekly Hours 40 Employee Type Regular Work Shift 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. 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.