Research Assistant II Brigham and Women's HospitalResearch Assistant IIBrookline, MA$24.28–$39.43 / hourSpecific tasks will include working with a Project Manager to finalize study protocols, oversee communications with IRBs, recruit patients, administer phone screens, administer informed consent, enroll patients, perform data collection, interpretation, and manuscript preparation, and manage the experience of subjects throughout a study. The Research Assistant II (RA II), to be based in the Osher Center's Mind-Body-Movement Laboratory, will work directly with the Project Manager and Director of the Osher Center for Integrative Health to advance the Center by performing a variety of tasks.
Manager, Patient Safety Parexel International CorpManager, Patient SafetyMAWith 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. Through team development, client partnership, cross-functional collaboration, and continuous improvement, you will help deliver high-quality safety services that are essential to clinical research and patient protection.
Post Doctoral Research Fellow Brigham and Women's HospitalPost Doctoral Research FellowBelmont, MAThe NVU-including brain endothelial cells, pericytes, astrocytes, microglia, neurons, and the vascular basal lamina-is positioned at the interface between systemic and neural processes and may play a critical role in translating immune, metabolic, and other stress-related challenges into altered neural function and psychiatric symptoms. The Core Manager will oversee the overall functioning of the facility, coordinate instrument access and maintenance, train and support users, supervise contracted technical services, and serve as a liaison among investigators, hospital administrative units, vendors, and external service providers.
Manager, Clinical Quality Services PCI Pharma ServicesManager, Clinical Quality ServicesBridgewater, Massachusetts$95,360–$107,280 / yearIn supportofand under the direction of the Director of Clinical QualityServices, the Manager, QualityClinicalServices helps toplan, direct,andcoordinatetheQuality activities of a designated Clinical Customer Focused Team toensurethatthegoals and objectives of the team are accomplished withintheprescribed time frames andwithinbudget. This rolewillsupervise, empower, coach, develop andhelp toretain a team of qualified individualsincludingQuality Specialist(s) and Quality Inspector(s)while partnering with thePCI-BostonClinical Project Management team(s) to ensurethat we deliver a qualityproduct/ serviceon time.
Associate Territory Manager - Connecticut - Western Massachusetts IQVIA Holdings IncAssociate Territory Manager - Connecticut - Western MassachusettsBoston, MA$55,000–$60,000 / yearYou will spend your days in the field calling on outpatient urology, urogynecology, and other associated outpatient clinics, building relationships with physicians, advanced practice providers, and clinic staff, and driving prescriptions of intermittent catheters and Urinary Management Systems. Success in this role comes from disciplined prospecting, high call volume, strong clinical messaging (we will teach you the clinical side), and the persistence to turn a first conversation into a prescribing relationship.
Trial Master File (TMF) Associate Oruka TherapeuticsTrial Master File (TMF) AssociateWaltham, California$104,000–$125,000 / yearThe TMF Associate serves as a key partner to Clinical Operations, CROs, vendors, and study teams, ensuring TMF records are complete, accurate, contemporaneous, and maintained in accordance with ICH-GCP guidelines, regulatory requirements, and company procedures. Oruka’s mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year.
NewResearch Budget Specialist - Cardiology Iterative Scopes Inc.Research Budget Specialist - CardiologyCambridge, MAThe Clinical Research Budgets Specialist is a critical operational partner to the sites within Iterative Health's growing domestic and international network - owning the development, review, and negotiation of clinical trial budgets and contract payment terms on their behalf. This role sits at the intersection of site operations, finance, and sponsor relationships, requiring someone who can interpret complex study protocols, navigate country-specific financial considerations, and drive budget discussions to resolution across multiple geographies simultaneously.
Staff Clinical Scientist WhoopStaff Clinical ScientistBoston, MA$170,000–$220,000 / yearRaise the scientific bar across the Clinical organization by mentoring Clinical Scientists and Senior Clinical Scientists, identifying scientific risks and opportunities, and contributing to WHOOP's longer-term clinical research and evidence-generation roadmap. This role is ideal for an experienced clinical scientist who combines deep expertise in study design, statistics, clinical evidence generation, and scientific communication with the ability to influence strategy across a highly cross-functional organization.
In-House Clinical Research Associate Alira HealthIn-House Clinical Research AssociateBoston, MA$50,000–$70,000 / yearIn-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. The final offer will be determined within the applicable location-specific range and will depend on the candidate's confirmed work location, relevant experience, skills, qualifications, internal equity, and role scope.
Clinical Research Associate Alira HealthClinical Research AssociateFramingham, MassachusettsCRAs work closely with the In-house CRAs, Lead CRAs, Director of Clinical Monitoring and Project Managers to ensure sites’ protocol compliance, address site questions, and assist with study recruitment, site training, and other site-related issues. Prepares consistently accurate and timely monitoring visit reports documenting site-related problems, resolutions, actions taken, protocol deviations, study progress, and enrollment status.
NewAssociate Director, Clinical Development Project Manager - Oncology GSK plcAssociate Director, Clinical Development Project Manager - OncologyWaltham, MARemote$139,425–$232,375 / yearCommunication, Cross-Departmental Collaboration, Decision Making, Financial Acumen, Innovation, Leadership, Project Controls, Project Management, Project Management Governance, Project Planning, Project Tracking, Risk Management, Stakeholder Engagement, Stakeholder Management, Strategic Leadership. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success.
Genetic Counselor Dana-Farber Cancer Institute IncGenetic CounselorBOSTON, MA$107,291–$124,033 / yearThe Genetic Counselor II provides genetic counseling services to patients and families within the Center for Genetics & Prevention and the Pediatric Cancer Genetic Risk Program under the leadership of the Clinical Director, Disease Center Leader, Associate Director of Genetic Counseling, and Genetic Counseling Managers. Provides consultation support for patients in other Dana-Farber disease centers, clinics, satellite locations, and affiliate settings, and aids in the professional development of genetic counseling interns, medical students, and other healthcare providers.
Director, Field Medical / Medical Science Liaison - New England KardiganDirector, Field Medical / Medical Science Liaison - New EnglandBoston, Massachusetts$265,000–$345,000 / yearThe individual acts as a scientific expert in cardiovascular disease (e.g., heart failure, cardiomyopathies, hypertension, cardiometabolic disease, etc.), builds trusted partnerships with key opinion leaders (KOLs), and implements the Cardiovascular Medical Strategy locally. Provide clinical trial support for company sponsored trials, facilitating relevant medical activities and working cross-functionally with Medical Affairs and Clinical Operations colleagues.
Protocol Scheduler Dana-Farber Cancer Institute IncProtocol SchedulerBOSTON, MA$45,500–$54,400 / yearAs all patients in this job family shall be considered high risk or falling under highly regulated services, this job family is responsible for carrying out specialized tasks to support regulatory requirements and patient safety, requiring an understanding of the sequential processes involved in clinical trials and patient treatment plans that fall under specified regulatory controls. Assigned to work with a clinical practitioner group consisting of physicians, physician's assistants, program nurses and nurse practitioners and other care providers, the individuals in this position will play a critical role in facilitating all aspects of patient care and maintaining compliance with protocol requirements.
Director, Clinical Scientist - Immunology AstraZeneca PlcDirector, Clinical Scientist - ImmunologyCambridge, MA$203,709.60–$305,564.40 / yearConduct AESI reviews and trending (these include CRS, neurotoxicity/ICANS, infections, IEC-HS, IEC-associated colitis, and new malignancies), prepare SRC, IDMC, and DMC safety packets, and flag emerging signals promptly with proposed next steps, bringing medical-judgement items to the Study Physician. Draft and review clinical sections of regulatory documents and responses, including HA interactions, briefing books, IND and annual reports, PIPs, and safety updates, ensuring SLMOP-driven surveillance outputs are reflected accurately and aligned with GCP, ICH, FDA, and EMA expectations.
Registered Nurse (RN), Inpatient Oncology Per Diem Dana-Farber Cancer Institute IncRegistered Nurse (RN), Inpatient Oncology Per DiemCambridge, MA$44.14–$109.51 / hourParticipate in quality and safety activities (e.g., safety huddles, infection prevention, hazardous drug handling, Joint Commission readiness) and support clinical research protocols as applicable (e.g., protocol adherence, specimen handling, adverse event reporting). 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.
Registered Nurse (RN), Inpatient Oncology Dana-Farber Cancer Institute IncRegistered Nurse (RN), Inpatient OncologyCambridge, MA$42.65–$105.81 / hourParticipate in quality and safety activities (e.g., safety huddles, infection prevention, hazardous drug handling, Joint Commission readiness) and support clinical research protocols as applicable (e.g., protocol adherence, specimen handling, adverse event reporting). 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.
Clinical Nurse Manager, Emergency Department St. Joseph Hospital NashuaClinical Nurse Manager, Emergency DepartmentNashua, New Hampshire$93,187.07–$128,333.13 / yearEstablishes and measures general and unit specific competencies in collaboration with clinical education, and provides opportunity for staff members to achieve their required competencies. Facilitates the Unit Advisory Committee activities to address issues relevant to staff members within the unit/department, promoting shared governance.
Clinical Specialist Lucid DiagnosticsClinical SpecialistBoston, MassachusettsThis includes but is not limited to: Hands-on training of other healthcare providers in the administration of EsoCheck® to indicated patients; Leading peer-to-peer engagements and small-group educational events. CLINICAL SPECIALIST: The Clinical Specialist role primarily covers the Eastern region of the United States, and is 100% field based, requiring 65%+ travel.
Senior Director, Clinical Translational Scientist Kiniksa PharmaceuticalSenior Director, Clinical Translational ScientistLexington, MAKiniksa is seeking an accomplished and strategic Senior Director, Clinical Translational Scientist reporting to GVP, Research & Non-Clinical Development to play a critical leadership role in advancing clinical-stage development programs from early clinical development through proof-of-concept and registrational studies. This individual will serve as a key scientific leader across multidisciplinary teams, integrating insights from Research, Clinical Development, Clinical Pharmacology, Bioanalysis, Biostatistics, Regulatory Affairs, and Medical Affairs to maximize the probability of technical and regulatory success across the portfolio.