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.
Workforce ConnectionsHealthcare Recruiter (Clinical & Research Talent) Workforce ConnectionsHealthcare Recruiter (Clinical & Research Talent)Boston, MA$40–$48 / hourContractorA nationally recognized pediatric academic medical center is seeking an experienced Recruiter to support hiring across clinical research and related scientific roles. This individual will partner closely with hiring managers and research leadership to attract and hire top-tier talent supporting groundbreaking research initiatives.
South Shore HealthNewRN Clinical Research Nurse / Dana-Farber Cancer Center South Shore HealthRN Clinical Research Nurse / Dana-Farber Cancer CenterMarshfield, 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- Neurology/Psychiatry Takeda PharmaceuticalAssociate Medical Director, Clinical Science, NS TAU- Neurology/PsychiatryCambridge, MAProvides 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.
CSL SeqirusNewAssociate Director, Clinical Assay Strategy, Flu CSL SeqirusAssociate Director, Clinical Assay Strategy, FluWaltham, MA$179,000–$212,000This role is intended for a recognized subject matter expert who understands the scientific, operational, and regulatory evolution of influenza immunogenicity assessment, including HAI, microneutralization (MN), ELLA, and multiplex platforms, and can strategically navigate assay modernization while maintaining regulatory alignment. Headquartered in Melbourne, Australia, with major manufacturing hubs in Holly Springs, NC, and Liverpool, UK, the company operates the world’s largest cell-based vaccine facility and serves as a primary partner to governments for global pandemic preparedness.
JobotNewVice President Clinical Development Ophthalmology JobotVice President Clinical Development OphthalmologyBoston, MA$350,000–$400,000 / 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. 4. Collaborate with cross-functional teams including regulatory affairs, pharmacovigilance, and medical affairs to ensure a holistic approach to product development.
Takeda PharmaceuticalNewAssociate Medical Director, Clinical Science, NS TAU Takeda PharmaceuticalAssociate Medical Director, Clinical Science, NS TAUCambridge, MAProvides 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 PharmaceuticalNewDirector, Clinical Outcomes Assessment, Global Evidence & Outcomes Takeda PharmaceuticalDirector, Clinical Outcomes Assessment, Global Evidence & OutcomesBoston, MARemote$177,000–$278,080 / yearDevelop, assess and interpret COAs, including Patient-Reported Outcomes (PROs), Observer-Reported Outcomes (ObsROs) and Clinician-Reported Outcomes (ClinROs), and performance outcome (PerfO) measures to derive clinical benefit during the clinical development and commercialization of new molecules, including development and validation of PRO and health-related quality of life instruments. Perform relevant research activities that may include, but not be limited to:Design, execution, and analysis in whole or in part of longitudinal prospective observational or randomized clinical trials evaluating clinical, and/or patient-centered endpoints; Targeted or comprehensive systematic literature reviews.
Takeda PharmaceuticalNewMedical Director, Clinical Science - Solid Tumor Takeda PharmaceuticalMedical Director, Clinical Science - Solid TumorBoston, MAAssesses scientific, medical, and development feasibility, evaluating strategic fit with overall portfolio, evaluating complete or ongoing clinical trials, assessing regulatory interactions and future development plans, interacting with upper management of potential partner/acquisition companies during DD visits and alliance negotiations, and representing clinical science on internal assessment teams in conjunction with TPNA/TPEU/TPC. These responsibilities include leadership roles in meetings with the regulatory organizations or 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.
REACH Beyond Domestic Violence IncNewClinical Supervisor REACH Beyond Domestic Violence IncClinical SupervisorWaltham, MA$74,000–$77,000 / yearThe role of the clinical supervisor is multifaceted; mitigating the impact of vicarious trauma on our team of staff, ensuring the staff, most of whom are not clinicians, provides consistent support to survivors in alignment with best practices, and strengthening programs and organizational capacity to address barriers and meet the needs of survivors. Comprehensive benefits package options including: Robust benefits including health, dental, vision, Flexible Spending Account (FSA), Health Reimbursement Account (HRA), Dependent Care Account (DCA), employer paid Long Term Disability, employer paid Employee Assistance Program, employer paid life Insurance, and retirement plan with employer matching up to 3% of salary contributed.
AramarkNewClinical Dietitian - Tewksbury Hospital AramarkClinical Dietitian - Tewksbury HospitalTewksbury, MA$65,000–$70,000 / yearSo, no matter what you're pursuing - a new challenge, a sense of belonging, or just a great place to work - our focus is helping you reach your full potential. BENEFITS: Aramark offers comprehensive benefit programs and services for eligible employees including medical, dental, vision, and work/life resources.
Jazz PharmaceuticalsNewSr Medical Science Liaison - Epilepsy (Boston) Jazz PharmaceuticalsSr Medical Science Liaison - Epilepsy (Boston)Boston, MAThe successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. See Jazz Pharma Privacy Policy at https://www.icims.com/legal/privacy-notice-website/ and SonicJobs Privacy Policy at https://www.sonicjobs.com/us/privacy-policy and Terms of Use at https://www.sonicjobs.com/us/terms-conditions.
Massachusetts Eye and Ear Infirmary - MEINewProgram Manager - Gene Editing & Therapy Massachusetts Eye and Ear Infirmary - MEIProgram Manager - Gene Editing & TherapyBoston, MAThe ideal candidate will oversee cross-functional teams, manage collaborations with external partners (CROs, academic institutions, and biotech companies), and ensure timely and compliant execution of preclinical projects that support early therapeutic development. NoLicenses and CredentialsExperienceResearch Related Experience 5-7 years required and Supervisory Experience 1-2 years preferredKnowledge, Skills and Abilities- Ability to make independent effective decisions.-
Harvard Medical Faculty Physicians at Beth Israel Deaconess Medical Center, Inc.Academic Medical Dermatologist Harvard Medical Faculty Physicians at Beth Israel Deaconess Medical Center, Inc.Academic Medical DermatologistBoston, MAIn addition to providing comprehensive care in the General Dermatology clinics, the Department also offers 16 subspecialty clinics and programs including atopic dermatitis, patch testing, hidradenitis suppurativa, high risk, pigmented lesions and melanoma. Our department of 17 dermatologists provides unique opportunities for medical dermatologists to practice and teach at the Medical Center in the Longwood Medical Area and in our department’s state-of-the-art practices in Chestnut Hill and/or Needham.
Beth Israel Deaconess Medical CenterNewTotal Joint Replacement Surgeon Beth Israel Deaconess Medical CenterTotal Joint Replacement SurgeonBoston, MAClinical practice will be primarily based at Beth Israel Deaconess Medical Center, a Level I trauma center in the heart of Boston’s Longwood Medical Area, and New England Baptist Hospital, with additional clinical opportunities for practice at other sites within the Beth Israel Lahey Health network, including BIDMC Needham, other BILH affiliates, as well as affiliated Ambulatory Surgical Centers. The Carl J Shapiro Department of Orthopedic Surgery at Beth Israel Deaconess Medical Center (an affiliate of Beth Israel Lahey Health) and Harvard Medical School seek applications and nominations for an early to mid-career Arthroplasty and Joint Reconstruction Surgeon with a strong interest in orthopaedic education and clinical research.
Beth Israel Deaconess Medical CenterNewEndowed Chair in Osteoporosis at Beth Israel Deaconess Medical Center Boston, Massachusetts Beth Israel Deaconess Medical CenterEndowed Chair in Osteoporosis at Beth Israel Deaconess Medical Center Boston, MassachusettsBoston, MAThe Division of Endocrinology, Diabetes & Metabolism in the Department of Medicine at Beth Israel Deaconess Medical Center (BIDMC), a Harvard Medical School (HMS) affiliated institution, seeks to recruit a senior clinician/clinical researcher to fill an endowed chair in the area of osteoporosis and metabolic bone disease. Responsibilities will include developing and maintaining a research portfolio in any aspect of metabolic bone disease, some ambulatory practice, teaching medical students, residents, and endocrine fellows, and assisting with community outreach.
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.
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.
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.
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 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 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.
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.
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.
Boston Medical CenterNewClinical Research Coordinator I, General Internal Medicine (part time) Boston Medical CenterClinical Research Coordinator I, General Internal Medicine (part time)Boston, MA$18.27–$25.72 / hourThe CRC I 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, and participates with the research team in preparation of data and other reports. This includes education, experience, skills, and certifications/licensures as they directly relate to position requirements; as well as business/organizational needs, internal equity, and market-competitiveness.
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, 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.
Tufts UniversityClinical Research Nurse - Human Nutrition Research Center on Aging Tufts UniversityClinical Research Nurse - Human Nutrition Research Center on AgingBoston, MassachusettsRegistered dietitians and dietary support staff develop and implement the dietary component of research protocols, which includes strict feeding protocols created in the MRU research kitchen with careful food intake monitoring throughout the duration of each study. The primary function of the Clinical Research Nurse is to conduct human research protocols, in a carefully monitored, controlled, yet dynamic environment to achieve quality outcomes for data and volunteer safety to support the HNRCA research goals.
Brigham and Women's HospitalNewClinical Research Coordinator I Brigham and Women's HospitalClinical Research Coordinator IBoston, MASummary: 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. The research coordinator's primary responsibility in the MGH Diabetes Research Center will be working on studies related to pregnancy and/or diabetes including those that use oral glucose tolerance testing and continuous glucose monitoring and collect biospecimens.
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.
Brigham and Women's HospitalNewClinical Research Coordinator 1 Brigham and Women's HospitalClinical Research Coordinator 1Boston, MAFollowing 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 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.
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 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.
Boston Children's HospitalNewResearch Intern - Surgical Clinical Research Core Boston Children's HospitalResearch Intern - Surgical Clinical Research CoreBoston, MAThe Surgical Clinical Research Core at Boston Children’s Hospital supports the research mission of the Department of Surgery by providing access to a wide range of research tools, collaborating with providers to develop new studies, and coordinating multiple ongoing projects. This position provides hands-on exposure to clinical research and offers opportunities to work closely with investigators, clinicians, and research staff in support of ongoing surgical research projects.
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.
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 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 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 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.
SanofiSenior Clinical Research Director, Rare SanofiSenior Clinical Research Director, RareCambridge, MA$225,000–$375,000 / yearBe the medical reference in the Clinical Study team, ensuring the medical relevance of the clinical data and able to act as mentor for other DMDs/DSDs/CSs, has the capacity to train them on the medical/scientific strategy by indication Key responsibilities include: Leading the clinical development plan strategies: Responsible for the clinical development plans and clinical sections of integrated development plans (IDP) Contribute in the definition of the product value proposition (TVP), Target Product Profile (TPP) and market access strategy (in collaboration with respective functions) and the focus of the research strategy, by providing input on existing clinical needs and approaches to clinical development strategies for research projects Prepares Internal Governance documents and contributes to the medical aspects the TPP, TVP and other GPT documents related to one or several indications of the IDP in support of the GPH Collaborate with other DMDs/DSDs within the project, ensures leadership, builds consensus, coordinates action plans with stakeholders to resolve project-related issues, anticipates potential issues (sharing lessons learned) across the project or study teams Raise study or project-level issues to the project head and propose related corrective action plans Collaborates with external partners, regulators, scientific experts and internal stakeholders Provide operational expertise to project clinical sub team, as needed Evaluates relevant medical literature and status from competitive products Lead, Support and oversee the execution of clinical development and studies activities Collaborate and communicate appropriately with all function stakeholders (e.g. Main Responsibilities:The role of the Senior CRD is to: Provide medical expertise in the Study team to conduct the clinical studies from early phases to LCM programs Collaborate with other medical and clinical scientific experts CRDs or DSDs in the project under the leadership of the Global Project Head, with the Global safety Officer, Regulatory Strategist and other key functional representatives to deliver development strategy and prepare/assist with regulatory bodies interaction Develop the study level regulatory documentation (Abbreviated Protocol, Protocol, Amended protocol) for their project, lead other operational development activities pertaining to study start-up (e.g.
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.
Integrated Resources, IncSenior Medical Director Clinical Research - Neurodegeneration Integrated Resources, IncSenior Medical Director Clinical Research - NeurodegenerationCambridge, MAThis is an opportunity to provide clinical leadership in developing RNAi therapeutics in client rapidly expanding portfolio, which spans the areas of rare genetic diseases, cardio-metabolic diseases, neuroscience, hematology and hepatology. The Senior Director, Clinical Research, will work in a matrix organization across Regulatory, Biostatistics, Clinical Operations, Preclinical, Commercial & QA teams to ensure fully harmonized and integrated development strategies.
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.
Science 37Per Diem Clinical Research Nurse - Home Visits Science 37Per Diem Clinical Research Nurse - Home VisitsManchester, NH$50–$55 / hourWith interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.
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.
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.