1,708 Results for

Clinical Research Jobs in Burlington, MA

Jobs

New!

Boston, MA1 day ago

$120,000–$140,000 Per Year

Information 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.

New!

Hamilton, MA2 days ago

$65–$65

Please contact Ashley Sin at (303) 317-5486 x486 or at ashley.sin@emvenio.com today to learn more about our opportunities where you can make a difference in your own career! Two (2) years' experience in starting and performing Phlebotomy/Peripheral Blood Draw, IVs, and Subcutaneous Injections (date of last practice within 6 months, preferred) .

Quincy, MA9 days ago

In 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.

New!

Boston, MA1 day ago

$350,000–$400,000 Per Year

Information 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.

New!

Cambridge, MA3 days ago

$198,500–$311,850 Per Year

Provides 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.

New!

Boston, MA3 days ago

$237,200–$372,790 Per Year

Assesses 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.

Watertown, MA7 days ago

Work 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.

New!

Boston, MA3 days ago

$25–$28 Per Hour

Project 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.

New!

Cambridge, MA2 days ago

Remote

$237,200–$372,790 Per Year

Assesses 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 GPLS & Business Units. 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.

Tewksbury, MA16 days ago

$65,000–$70,000

New!

Boston, MA2 days ago

$69,669–$104,503

Assume 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.

New!

Dedham, MA2 days ago

$102,162–$153,244

Assume 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.

New!

Waltham, MA1 day ago

$189,000–$224,000

We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. Prepare abstracts, posters, oral presentations and written reports to effectively communicate results of clinical programs and studies to internal and external stakeholders and colleagues with varying levels of clinical research knowledge.

New!

BOSTON, MA6 days ago

Our seamless in-office and 24/7 virtual care services, on-site labs, and programs for preventive care, chronic care management, common illnesses and mental health concerns have been delighting people for the past fifteen years. Enrolled in, or have completed, an accredited Internal or Family Medicine residency programPracticed at least 2 of the last 5 years in an outpatient primary care setting.

New!

BOSTON, MA6 days ago

Our seamless in-office and 24/7 virtual care services, on-site labs, and programs for preventive care, chronic care management, common illnesses and mental health concerns have been delighting people for the past fifteen years. Employee Assistance Program - Free confidential services for team members who need help with stress, anxiety, financial planning, and legal issues.

BOSTON, MA14 days ago

New!

BOSTON, MA6 days ago

Our seamless in-office and 24/7 virtual care services, on-site labs, and programs for preventive care, chronic care management, common illnesses and mental health concerns have been delighting people for the past fifteen years. Employee Assistance Program - Free confidential services for team members who need help with stress, anxiety, financial planning, and legal issues.

Boston, MA14 days ago

In 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.

Boston, MA9 days ago

Clinical 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.

Boston, MA9 days ago

The 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, MA13 days ago

$20.16–$29.01 Per Hour

The 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.

Boston, MA30+ days ago

Full-time

Overview 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, Massachusetts14 days ago

The 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.

Boston, MA30+ days ago

$47,500–$66,500 Per Year

The 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, MA30+ days ago

$110,000–$135,000 Per Year

Responsibilities 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.

Cambridge, MA30+ days ago

Remote

Flexible 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.

Boston, MA30+ days ago

Applicants 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.

Boston, Massachusetts30+ days ago

Candidates 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.

Cambridge, MA30+ days ago

$105,600–$158,400 Per Year

Independently 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.

Boston, MA30+ days ago

$55,000–$70,000 Per Year

In-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.

Framingham, MA30+ days ago

$55,000–$70,000 Per Year

Boston, Massachusetts30+ days ago

The 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.

Boston, MA11 days ago

$41,246.40–$61,339.20 Per Year

The Neurofibromatosis Research Initiative (NFRI) within the Division of Genetics and Genomics at Boston Children's Hospital is seeking a Clinical Research Assistant to facilitate recruitment of participants in clinical research studies related to Neurofibromatosis Type 1 (NF1). Third, we are recruiting participants with NF1 who are at higher risk of NF1-related tumors to prospectively collect blood samples that will be analyzed for early markers of tumor development (a so-called "liquid biopsy").

Boston, MA30+ days ago

$282,200–$444,200 Per Year

The Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area, specifically in our Hematology Section. The Senior Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies.

Boston, MA30+ days ago

Responsibilities 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, MA30+ days ago

With 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.

MA30+ days ago

Work 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.

Boston, MA18 days ago

$15–$51.94 Per Hour

Position Summary: The 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, MA30+ days ago

Registered 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.

Waltham, MA30+ days ago

$99,000–$121,000 Per Year

Partner 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.

Boston, MA30+ days ago

$41,246.40–$61,339.20 Per Year

Position Summary: The 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, MA30+ days ago

$21.63–$31.25 Per Hour

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. Extracts data on protocol subjects from hospital records, outpatient charts and private physician office records in order to complete case report forms required by specific protocols.

Boston, MA30+ days ago

$21.63–$31.25 Per Hour

Boston, MA19 days ago

$255,800–$402,700 Per Year

The Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies. The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the ophthalmology therapeutic area.

Boston, MA30+ days ago

$255,800–$402,700 Per Year

The Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within their area of expertise, in terms of new scientific findings, research methodologies. Job Description: The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Immunology therapeutic area.

Boston, MA30+ days ago

$255,800–$402,700 Per Year

Boston, Massachusetts30+ days ago

Andover, MA15 days ago

Perform 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.

Roxbury, MA30+ days ago

The 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.

Burlington, MA30+ days ago

$19.23–$30.77 Per Hour

Submits all IRB submission documents such as protocol amendments and consent form revisions, annual reviews, adverse events, investigator changes, accrual status change and change in risk to the IRB in a timely manner with moderate assistance/guidance from senior staff; Complies with IRB decisions, conditions and requirements. Completes source worksheets and case report forms (CRFs) as dictated by the assigned research study (i.e. required forms in the required format in the required time interval); Ensures CRF's and source are complete and done correctly.

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Clinical Research Jobs in Burlington, MA

Sr. Oncology Clinical Research Associate Jobot

Registered Nurse Pediatric Clinical Research Professional Case Management

RN Clinical Research Nurse / Dana-Farber Cancer Center South Shore Health

Vice President Clinical Development Ophthalmology Jobot

Associate Medical Director, Clinical Science, NS TAU Takeda Pharmaceutical

Medical Director, Clinical Science - Solid Tumor Takeda Pharmaceutical

Associate Director, Clinical Operations Clinical Dynamix, Inc.

Research Coordinator Joulé

Medical Director, Clinical Science, NS TAU- Sleep Medicine Takeda Pharmaceutical

Clinical Dietitian - Tewksbury Hospital Aramark

Clinical Nurse Coordinator- PT Nights Hebrew SeniorLife

Clinical Nurse Coordinator Hebrew SeniorLife

Associate Director, Biostatistics CSL Behring

Per Diem Family Medicine Physician (Casual Employee) One Medical

Per Diem Nurse Practitioner or Physician Assistant (Casual Employee) One Medical

Per Diem Primary Care Physician (Casual Employee) One Medical

Per Diem Family Nurse Practitioner or Physician Assistant (Casual Employee) One Medical

Academic Medical Dermatologist Harvard Medical Faculty Physicians at Beth Israel Deaconess Medical Center, Inc.

Total Joint Replacement Surgeon Beth Israel Deaconess Medical Center

Endowed Chair in Osteoporosis at Beth Israel Deaconess Medical Center Boston, Massachusetts Beth Israel Deaconess Medical Center

Clinical Research Associate Brigham and Women's Hospital

Clinical Research Coordinator I (Clinical, Behavioral & Research Outcomes) Joslin Diabetes Center

Clinical Research Associate Mass General Brigham

Clinical Research Coordinator III, Clinical Research Network Boston Medical Center

Oncology Clinical Research Associate Zp Group Llc

Senior Clinical Research Associate ICON Plc

Experienced Clinical Research Associate Hematology/Oncology Medpace Holdings Inc

Experienced Clinical Research Associate - Hematology/Oncology Medpace, Inc.

Senior Clinical Research Associate eGenesis Inc

In-House Clinical Research Associate-2 Alira Health

In House Clinical Research Associate Alira Health

Clinical Research Associate Alira Health

Clinical Research Assistant- Neurofibromatosis Research Initiative Boston Children's Hospital

Senior Clinical Director, Clinical Research, Hematology Merck & Co Inc

Research Assistant II - Clinical Research Unit Boston Medical Center

Sr. Clinical Research Associate Getinge AB

Senior Clinical Research Associate - Oncology - US - FSP Parexel International Corp

Research Intern - Surgical Clinical Research Core Boston Children's Hospital

Clinical Research Nurse - Human Nutrition Research Center on Aging Tufts University

In House Clinical Research Associate Ardelyx Inc

Clinical Research Assistant - CAIR and HPNP Boston Children's Hospital

Center for Anesthesia Research Excellence (CARE): Clinical Research Coordinator II Lahey Hospital and Medical Center

Clinical Research Assistant II, Center for Anesthesia Research Excellence (CARE) Lahey Hospital and Medical Center

Clinical Director, Clinical Research, Ophthalmology Merck & Co Inc

Clinical Director (Principal Scientist), Clinical Research, Immunology - Rheumatology Merck & Co Inc

Clinical Director, Clinical Research, Hematology Merck & Co Inc

Clinical Research Assistant II, Center for Anesthesia Research Excellence (CARE) Beth Israel Lahey Health

Clinical Research Coordinator I Ora

Clinical Research Coordinator II Boston Medical Center

Clinical Research Coordinator I with Translational Research Lahey Hospital and Medical Center

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