Assistant/Associate Professor of Practice (Non-tenure), Department of Physical Therapy Simmons UniversityAssistant/Associate Professor of Practice (Non-tenure), Department of Physical TherapyBoston, MARemote$94,159–$103,093 / yearA terminal academic doctorate (PhD, EdD, ScD, etc.) is preferred; A doctoral degree in physical therapy (DPT) or a related field is required; Active, unrestricted license to practice physical therapy in any United States jurisdiction; Evidence of excellence in professional practice (ABPTS specialty certification is desirable) and a high potential for excellence in teaching and service; At least 5 years of applicable clinical experience for Assistant Professor of Practice; At least 10 years of applicable clinical experience for Associate Professor of Practice; Physical therapy teaching experience preferred. Interested candidates should submit the following electronically with their application: (1) a letter of application addressing teaching experiences, (2) teaching philosophy, course or content interests, and clinical/professional interests and expertise; (3) research statement, and (4) curriculum vitae.
Registered Nurse, Clinical Delivery Care AccessRegistered Nurse, Clinical DeliveryBoston, MARemote$34–$48 / hourWith 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. Furthermore, they serve as a point of escalation for the Member Services team, addressing complex inquiries related to lab results and assisting in the resolution of patient concerns by providing clinical insights and ensuring patients receive accurate information and appropriate follow-up.
Clinical Trials Monitor I Dana-Farber Cancer Institute IncClinical Trials Monitor IBrookline, MARemote$62,200–$74,200 / yearThe Clinical Trials Monitor helps to ensure compliance of the clinical research enterprise with all related regulatory policies and guidelines, including federal, state, local, as well as the policies and procedures outlined by the Dana-Farber Cancer Institute and Dana-Farber Harvard Cancer Center (DF/HCC) consortium. 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.
Medical Writer Clinical Development The Fountain Group LLCMedical Writer Clinical DevelopmentMarlborough, MARemoteExperience authoring or reviewing Clinical Study Reports (CSRs), clinical study protocols, protocol amendments, and Investigator Brochures (IBs) . Integrate scientific and clinical information from Clinical Development, Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, Pharmacovigilance, and Medical Affairs functions.
Leader Medical Affairs Canon USA & AffiliatesLeader Medical AffairsBoston, MARemote10 years’ experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting or 3 years of experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting plus 7 years of experience in healthcare industry as imaging scientist or research manager. Analyze and communicate technical and clinical product specification requirements from luminaries, market research teams, and via Medical Advisory Boards (MABs) to global business team.
Job Posting Title Clinical Trial Psych Rater - German Speaking IQVIA Holdings IncJob Posting Title Clinical Trial Psych Rater - German SpeakingBoston, MARemoteOur team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews).
Clinical Trial Psych Rater - Hungarian Speaking IQVIA Holdings IncClinical Trial Psych Rater - Hungarian SpeakingDanvers, MARemoteOur team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews).
Medical Writer Clinical Development eTeam Inc.Medical Writer Clinical DevelopmentMarlborough, MARemoteCollaborate with cross-functional teams, including Clinical Development, Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, Pharmacovigilance, and Medical Affairs, to gather, interpret, and integrate scientific and clinical information into clear, accurate, and submission-ready documents. This role works closely with cross-functional stakeholders to ensure documents are scientifically accurate, strategically aligned, and delivered according to established timelines and medical writing plans.
Medical Writer Clinical Development Sunrise Systems IncMedical Writer Clinical DevelopmentMarlborough, MARemote$100–$112 / hourCollaborate with cross-functional teams, including Clinical Development, Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, Pharmacovigilance, and Medical Affairs, to gather, interpret, and integrate scientific and clinical information into clear, accurate, and submission-ready documents. This role works closely with cross-functional stakeholders to ensure documents are scientifically accurate, strategically aligned, and delivered according to established timelines and medical writing plans.
Regulatory Coordinator - Center of Early Detection & Interceptions Blood Cancers Dana-Farber Cancer Institute IncRegulatory Coordinator - Center of Early Detection & Interceptions Blood CancersBOSTON, MARemote$55,530–$61,700 / yearThis position will work collaboratively with a variety of personnel at all levels, including faculty and study team members of DF/HCC and external institutions, cooperative groups, clinical trials experts, representatives from the pharmaceutical industry, federal agencies, and other research organizations. The Regulatory Coordinators (RC) works under the direction of the Principal Investigator(s), Regulatory Operations Manager, Clinical Research Manager and / or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project.
Medical Science Liaison - Cardiovascular - Boston, MA Territory NovartisMedical Science Liaison - Cardiovascular - Boston, MA TerritoryBoston, MassachusettsRemoteThe primary responsibility of the MSL is to engage with customers - customer engagements may include but are not limited to: emerging data discussions, clinical trial activities, uncovering barriers in patient journey, understanding market dynamics within their territory, exploration of areas of unmet medical need, pipeline discussions, educating on disease state and product, capturing adverse events, and capturing medical insights through all stages of product lifecycle. The MSL must demonstrate deep therapeutic expertise, understand territory and market influences, engage scientifically with Healthcare Providers (HCPs) and medical experts, manage, and develop their territory and execute all relevant activities in alignment with the medical strategic and tactical plan – while functioning within the Novartis Code of Conduct, Ethics/Compliance policies and Working Practice documents.
Senior Machine Learning Engineer OneStudyTeamSenior Machine Learning EngineerBoston, MARemote$140,000–$190,000 / yearBy joining our team as a Senior Machine Learning Engineer , you will play a pivotal role in building cutting-edge AI products that directly impact how new therapies reach patients. What You'll Bring to OneStudyTeam: Minimum Experience: Minimum of 5+ years of hands-on experience building and deploying machine learning solutions in production at scale.
Senior Data Scientist OneStudyTeamSenior Data ScientistBoston, MARemote$140,000–$190,000 / yearDevelop Other Advanced Statistical Models: Create and refine predictive models (Bayesian inference, regression analysis, time-series forecasting) to address other key clinical trial challenges and improve decision-making. Patient Matching/Ranking Algorithms: Support projects to build algorithms that intelligently match patients to (or rank patients for) appropriate clinical trials, enhancing recruitment efficiency and patient inclusion.
Clinical Expert, Onco-Immunology BioptimusClinical Expert, Onco-ImmunologyBoston, MARemoteOnco-Immunology Expertise : Deep expertise in onco-immunology, including IO mechanisms, response and resistance biology, tumor microenvironment biology, IO combinations, and understanding of pharmaceutical pipelines and unmet clinical needs. You will contribute clinical and translational expertise to help identify the most important clinical questions and modalities to focus on, support the interpretation of model outputs, and advise on partnerships and research programs aligned with Bioptimus' data and scientific goals.
Senior Manager, Clinical Study Quality Lead (Hybrid) Vertex Pharmaceuticals, IncSenior Manager, Clinical Study Quality Lead (Hybrid)Boston, MARemote$137,800–$206,800 / yearGeneral Summary: The Senior Manager, Clinical Study Quality Lead provides study-level quality oversight for assigned clinical trials to help ensure they are conducted in compliance with Good Clinical Practice (GCP), applicable global regulations, study protocols, and Vertex procedures. This is an individual contributor role focused on GCP quality assurance oversight for clinical trials, including risk-based audit strategy, quality risk identification, issue escalation, CAPA support, compliance trend analysis, and inspection readiness.
Senior Manager, Clinical Study Quality Lead Vertex PharmaceuticalsSenior Manager, Clinical Study Quality LeadBoston, MassachusettsRemoteThe Senior Manager, Clinical Study Quality Lead provides study-level quality oversight for assigned clinical trials to help ensure they are conducted in compliance with Good Clinical Practice (GCP), applicable global regulations, study protocols, and Vertex procedures. This is an individual contributor role focused on GCP quality assurance oversight for clinical trials, including risk-based audit strategy, quality risk identification, issue escalation, CAPA support, compliance trend analysis, and inspection readiness.
NewClinical Trial Rater - Borderline Personality Disorder IQVIA Holdings IncClinical Trial Rater - Borderline Personality DisorderBoston, MARemoteThe potential base pay range for this role is The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). This role requires strong clinical judgment, experience with psychiatric populations, and the ability to maintain objectivity and inter‑rater reliability across multiple assessments and time points.
Sr. Medicare Coverage Analyst Dana-Farber Cancer Institute IncSr. Medicare Coverage AnalystBOSTON, MARemote$77,500–$90,400 / yearThe Medicare Coverage Analyst determines whether proposed clinical research studies are a Qualifying Clinical Trial as defined by the Medicare Clinical Trial Policy (NCD 310.1) and designates medical procedures/services based on relevant regulations and determinations. The Medicare Coverage Analyst (MCA) is responsible for reviewing clinical research protocols, Informed Consent Forms, Clinical Trial Agreements, and other relevant study-related documents to create a coverage analysis/billing guide.
Principal Clinical Content- Physician - Uptodate, Physician Editor, Neurology Wolters KluwerPrincipal Clinical Content- Physician - Uptodate, Physician Editor, NeurologyWaltham, MARemote$173,500–$310,000 / yearUpToDate editors work closely with outside authors, section editors, editors-in-chief, and peer reviewers to ensure the material is accurate and free of bias. In the remaining 10 to 20% time, Physician Editors should continue patient care activities, using their clinical experience to help ensure the content of the program is maximally useful at the point of care.
Senior Director, AI Delivery & Operations Thermo Fisher Scientific IncSenior Director, AI Delivery & OperationsMARemote$167,500–$278,000 / yearAbout the Position: Reporting to the VP, Head of Analytics and AI, the Senior Director, AI Delivery & Operations is a senior leadership role responsible for building, operating and scaling CRG Digital's end-to-end AI engineering and platform capability, anchored in reusable architecture and scalable execution systems. Redefine engineering productivity by driving adoption of AI-assisted and agent-based development, including AI coding assistants (e.g., Codex-style tools), agent-enabled code generation, testing, and refactoring and automated documentation and code review workflows.