1,791 Results for

Clinical Research Jobs in Somerville, MA

Jobs

Boston, MA9 days ago

$120,000–$140,000 Per Year

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New!

Boston, MAToday

$70.02–$72.19 Per Hour

Coordinates with clinical research coordinators and collaborates with staff within respective disease groups and with outside organizations in the completion of clinical research trials. Position requires tact and diplomacy to successfully motivate/educate subjects and staff, and knowledge of research regulations and research compliance requirements, including Protection of Human Subjects.

New!

Boston, MA6 days ago

$125,000–$140,000 Per Year

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New!

Cambridge, MA2 days ago

Remote

$198,500–$311,850 Per Year

li>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, 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 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.

New!

Boston, MA2 days ago

li>Economics, Accounting, Finance, and Securities Analysis - Knowledge of economic, accounting, and financial principles and practices, the financial markets, the industry, the analysis and reporting of financial data, and associated terminology. Our award-winning analysts are thought leaders, many with hands-on experience in their respective industries, offering objective, in-depth analysis and timely, actionable research ideas.

Boston, MA11 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

$174,000–$212,000 Per Year

Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types.

Prime Medicine is seeking an experienced Associate Director of Clinical Data Management to lead clinical data strategy and execution across gene editing programs from first-in-human studies through regulatory submission.

New!

Boston, MA2 days ago

$221,600–$369,333 Per Year

li>The current base salary range for this position is expected to be between $221,600 and $369,333 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators.

Follow important developments and relevant trends in scientific literature and develop/maintain contracts with external experts to support understanding of the candidate drug effects and to gain strategic insights to the further development and placement of study and overall program.

Bridgewater, MA8 days ago

$165,000–$175,000 Per Year

This position coordinates effective administration of SOT services as further described below and provides administrative guidance and support to site SOT staff, reporting to the Director of Sex Offense Specific Program Services. VitalCore Health Strategies (VCHS), an industry leader in Correctional Health Care has an opening for a Full-Time Clinical Director in our Sex Offender Treatment Program at the Massachusetts Treatment Center in Bridgewater, MA.

Bridgewater, MA8 days ago

$75,000–$110,000 Per Year

CLINICAL THERAPIST ESSENTIAL FUNCTIONS Some of the core tasks completed by Clinical Therapists include: In collaboration with the patient, develop monitor and, when clinically indicated modify individualized treatment plans to reflect therapeutic needs/goals. CLINICAL THERAPIST POSITION SUMMARY The Clinical Therapist for sex offender treatment is responsible for providing sex offender specific and related treatment services to patients within the facility.

BOSTON, MA22 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.

BOSTON, MA14 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, MA5 days ago

p>The Division of Cardiology and the CardioVascular Center (CVC) at Tufts Medical Center in Boston is seeking a board-certified/board-eligible Cardiac Electrophysiologist to join a dynamic and expanding electrophysiology (EP) program.

Tufts Medicine is a leading integrated health system bringing together the best of academic and community healthcare to deliver exceptional, connected and accessible care experiences to consumers across Massachusetts.

New!

Massachusetts2 days ago

Partner 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 risks. Submit all required reports, documentation, updates and tracking within required timeframes, including but not limited to Trial Master File (TMF) documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management, study progress and metrics.

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

p>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.

Boston, MA30+ days ago

p>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, 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, Massachusetts30+ days ago

p style="margin:0px"> TWP 2024 CRO2024 .

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.

Danvers, MA30+ days ago

$109,000–$174,800 Per Year

li>Develop and deliver technical training on GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements as well as training and proctoring new employees on trial and study related activities.

Assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical Practices), PHI (Personal Health Information) and regulatory requirements.

MA30+ days ago

Remote

li>

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.

Cambridge, MA30+ days ago

$105,600–$158,400 Per Year

li>

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.

Framingham, 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.

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.

Boston, MA30+ days ago

$85,000–$120,000 Per Year

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, MA19 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, MA26 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

p>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.

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.

MA30+ days ago

$282,200–$444,200 Per Year

p>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

$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.

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, 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.

Manchester, New Hampshire30+ 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.

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

p>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

$48,100–$54,400 Per Year

The CRC (Clinical Research Coordinators) work within the Breast 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.

Boston, MA30+ days ago

$20.16–$29.01 Per Hour

Physical Requirements Standing Frequently (34-66%) Walking Frequently (34-66%) Sitting Occasionally (3-33%) Lifting Frequently (34-66%) 35lbs+ (w/assisted device) Carrying Frequently (34-66%) 20lbs - 35lbs Pushing Occasionally (3-33%) Pulling Occasionally (3-33%) Climbing Rarely (Less than 2%) Balancing Frequently (34-66%) Stooping Occasionally (3-33%) Kneeling Occasionally (3-33%) Crouching Occasionally (3-33%) Crawling Rarely (Less than 2%) Reaching Frequently (34-66%) Gross Manipulation (Handling) Frequently (34-66%) Fine Manipulation (Fingering) Frequently (34-66%) Feeling Constantly (67-100%) Foot Use Rarely (Less than 2%) Vision - Far Constantly (67-100%) Vision - Near Constantly (67-100%) Talking Constantly (67-100%) Hearing Constantly (67-100%). The Clinical Research Coordinator I will support multiple ongoing clinical research studies focused on the use of novel portable, low-field MRI and blood biomarker discovery, with an emphasis on Alzheimer's disease, in an outpatient clinic setting.

Boston, MA27 days ago

p>Key responsibilities include following up with enrolled participants by phone regarding survey responses; entering and maintaining participant data in the study database; processing and submitting participant payments; scheduling and coordinating study visits; assisting with recruitment efforts; and supporting Institutional Review Board submissions and other regulatory documentation.

Site: The Brigham and Women''s Hospital, Inc.

Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission.

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.

MA30+ days ago

$255,800–$402,700 Per Year

p>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 Oncology therapeutic area, specifically in our Hematology Section.

Boston, MA27 days ago

$255,800–$402,700 Per Year

p>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, Massachusetts30+ days ago

New!

Boston, MA6 days ago

Remote

$60,000–$90,000 Per Year

p>With 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.

We are looking for a Community Clinical Research Educator II who is deeply passionate about promoting awareness and education of clinical research, and access to clinical trials., to diverse communities.

Boston, MA30+ days ago

$20.16–$29.01 Per Hour

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 • 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.

Boston, MA30+ days ago

$27.09–$40.63 Per Hour

Reporting 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. experience with site management, study management, IRBs, and federal regulations regarding clinical research compliance requiredExperience in the coordination of intergroup or multi-site clinical studies preferred.

Boston, MA30+ days ago

$20.16–$29.01 Per Hour

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. 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.

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Clinical Research Jobs in Somerville, MA

Sr. Oncology Clinical Research Associate Jobot

Clinical Research Nurse II, Oncology Iconma

Sr. CRA (Oncology) Sponsor side! Jobot

Associate Medical Director, Clinical Science, NS TAU Takeda Pharmaceutical

Medical Director, Clinical Science - Solid Tumor Takeda Pharmaceutical

Research Associate II - Biotechnology Stifel

Research Coordinator Joulé

Associate Director, Clinical Data Management Prime Medicine, Inc.

Medical Director, Sickle Cell Disease, Clinical Development Agios Pharmaceuticals

Clinical Director - SOTP VitalCore Health Strategies

Clinical Therapist VitalCore Health Strategies

Per Diem Primary Care Physician (Casual Employee) One Medical

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

Per Diem Family Medicine Physician (Casual Employee) One Medical

Cardiac Electrophysiologist Tufts Medicine

Senior Clinical Research Associate/Clinical Research Associate II - Oncology - Northeast or Central US - FSP Parexel

Clinical Research Coordinator III, Clinical Research Network Boston Medical Center

Oncology Clinical Research Associate Zp Group Llc

Experienced Clinical Research Associate Hematology/Oncology Medpace Holdings Inc

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

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

Senior Clinical Research Associate Johnson & Johnson

Senior Clinical Research Associate ICON Plc

Senior Clinical Research Associate eGenesis Inc

In House Clinical Research Associate Alira Health

In-House Clinical Research Associate-2 Alira Health

Clinical Research Associate Alira Health

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

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

Sr. Clinical Research Associate Getinge AB

In House Clinical Research Associate Ardelyx Inc

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

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

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

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

Clinical Research Coordinator I Ora

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 Research Coordinator - Breast Oncology Clinical Trials Dana-Farber Cancer Institute Inc

Clinical Research Coordinator I (Alzheimer''''s Research) Brigham and Women's Hospital

Bilingual Clinical Research Coordinator I Pulmonary Research Brigham and Women's Hospital

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

Clinical Director, Clinical Research, Hematology Merck & Co Inc

Clinical Director, Clinical Research, Ophthalmology Merck & Co Inc

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

Community Clinical Research Educator II Care Access

Clinical Research Coordinator Brigham and Women's Hospital

Clinical Research Coordinator II Shriners Hospitals for Children

Clinical Research Coordinator I Brigham and Women's Hospital

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