Marketing Specialist Adams ClinicalMarketing SpecialistWatertown, MA$65,000–$80,000 / yearThe Digital Marketing Specialist will be responsible for helping to achieve company growth and profitability goals via implementation of improvements to marketing campaigns, performance analysis, and support for ongoing development to company marketing strategy. 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.
Lead Dosing Session Monitor Adams ClinicalLead Dosing Session MonitorBoston, MA$65–$76 / hourTherapists are expected to maintain consistent availability 3 days per week for participant-facing responsibilities, including pre-dose preparations, monitoring during dosing sessions, and post-dose follow-ups. We are seeking a Part-Time Psychedelic Dosing Monitor / Therapist to support clinical trials focused on psychedelic research for individuals with depression, anxiety, and other mood disorders at one or more of our research site locations.
Per Diem Nurse Practitioner Or Physician Assistant (Casual Employee) One MedicalPer Diem Nurse Practitioner Or Physician Assistant (Casual Employee)Boston, MAOur 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. All regular team members working 24+ hours per week and their dependents are eligible for benefits starting on the team member's date of hire: Taking care of you today.
Assistant Psychedelic Dosing Session Monitor Adams ClinicalAssistant Psychedelic Dosing Session MonitorBoston, Massachusetts$30–$40 / hourWe are seeking a per diem (PRN) Assistant Psychedelic Dosing Monitor to support clinical trials focused on psychedelic research for individuals with depression, anxiety, and other mood disorders at one or more of our research site locations. Minimum of 1 year of experience in a mental healthcare setting including clinical research experience as a Clinical Research Coordinator or in a comparable role supporting psychiatric research studies.
Psychiatric Nurse Practitioner/Physician Assistant Adams ClinicalPsychiatric Nurse Practitioner/Physician AssistantBoston, Massachusetts$125,000–$175,000 / yearIn addition, the Clinician – Medical Rater performs basic trial-related medical tasks—including physical and neurological examinations, review of laboratory reports and ECGs, adverse event (AE) assessment, and concomitant medication review—under the supervision of the PI and/or Sub-I. The Clinician – Medical Rater works closely with a multidisciplinary research team in a fast-paced clinical research environment to support high-quality data collection and successful trial execution.
Associate Director, Investor Relations Beam Therapeutics IncAssociate Director, Investor RelationsCambridge, MA$185,000–$225,000 / yearWork cross-functionally with R&D, Clinical Development, Regulatory, and Commercial teams to: stay current on program updates and key milestones; translate technical data into clear, investor-relevant narratives; and support investor-facing materials related to clinical data readouts, regulatory updates, and pipeline evolution. You will partner closely with senior leadership, finance, legal, corporate communications, and program teams to translate complex clinical and scientific milestones into clear, compelling, investor-ready messaging across earnings cycles, conferences, and one-on-one engagements.
Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health IncExperienced Clinical Research Associate - Sponsor DedicatedMATogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Clinical Trial Transparency Senior Associate Integrated Resources, IncClinical Trial Transparency Senior AssociateCambridge, MassachusettsContractorJob DescriptionJob Title: Clinical Trial Transparency Senior AssociateLocation: Cambridge, MA Duration: 7+ months (Possibility of extension)• Performs the Clinical Trial Registration and/or results disclosure activities for new and/or ongoing studies.• Clinical Trial Transparency Senior AssociateIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Clinical Research Coordinator II - Lowell General Hospital, Cancer Center - On-site Tufts MedicineClinical Research Coordinator II - Lowell General Hospital, Cancer Center - On-siteLowell, MassachusettsThe Clinical Research Coordinator supports clinical trials by recruiting and screening participants, conducting informed consent, and coordinating all protocol‑required visits, procedures, and follow‑up. Responsible for assisting with Institutional Review Board (IRB) requirements for each study including meeting institutional educational requirements, submitting documents for review, adverse event reporting and annual reviews.
HMS - Associate in Biomedical Informatics (Patel Lab) Harvard UniversityHMS - Associate in Biomedical Informatics (Patel Lab)Cambridge, MA$60,000–$80,000 / yearBasic Qualifications BS/MS in Data Science, Statistics, Computer Science, Epidemiology, Environmental Health, or a related field Demonstrated expertise in large-scale analysis and familiarity with health-related datasets Additional Qualifications Proficiency in statistical software (R, Python, etc.) and working knowledge of data management protocols Experience with exposome or environmental data, multi-omics integration, and exposure-wide association studies (ExWAS) and GIS preferred but not required. Learn with us Special Instructions Required documents: • Curriculum Vitae • Statement of Research for PhD work • Cover Letter describing your interest in the lab and initial ideas for new research directions or projects you could undertake in the lab • Note with names and contact information for three people who have agreed to serve as your reference Please submit application documents through the ARIeS portal.
Research Assistant II Boston Medical CenterResearch Assistant IIRoxbury, MADuties include but are not limited to, assisting with patient recruitment, scheduling study visits, consenting study subjects, administering questionnaires, delivering health literacy curriculum materials directly to study subjects, creating and filing case report forms, entering and updating data, maintaining databases, running reports, and performing other administrative tasks in support of the clinical studies. The Telehealth Epilepsy Care Collaborative (TECC) is recruiting a full-time Research Assistant II (RA2) to assist in the implementation of a project designed to improve mental health literacy, reduce stigma and foster resiliency in children and youth with epilepsy with comorbid mental illness served at Boston Medical Center (BMC).
Clinical Supply Associate Integrated Resources, IncClinical Supply AssociateLexington, MassachusettsFull timeEnsure that goals and objectives of projects are accomplished within established time frames and budget guidelines.• Ensure compliance with Good Manufacturing Practices and applicable state and federal regulatory authorities• Participate in protocol review to identify clinical issues; establish time frames; develop budget projections; identify procedural and administrative issues; recommend amendments to study protocols as appropriate.• Manage clinical supply activities including labeling, packaging, distribution of clinical trial supplies, randomization, development and maintenance of clinical trial database and drug accountability systems control.•
Human Factors Engineering (HFE) Lead - Associate Engineering Fellow (AEF) 3316 Takeda Development Center AmericasHuman Factors Engineering (HFE) Lead - Associate Engineering Fellow (AEF)Lexington, MassachusettsThe HFE Lead - AEF will be integral to design and development of product user interface including hardware, software, packaging, labeling, and instruction material to support safe and effective use of the product for the intended use by the intended users in the anticipated use environment. The HFE AEF will lead the advancement of AI-enabled Human Factors Engineering capabilities across the organization by identifying and prioritizing high-impact digital transformation initiatives aligned with pipeline and platform device strategies.
Clinical 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.
Sr.Clinical Operations Lead Integrated Resources, IncSr.Clinical Operations LeadCambridge, MassachusettsFull timePartnering with GCO Vendor Management to escalate issues, sharing best practices and leveraging the Vendor Operations Relationship Manager for issue resolution• Initiates, leads and shares best practice development in Phase planning and seeks opportunities for innovation and efficiency with the Clinical Operation Management group• Identifies interdependencies and synergies with other trials and programs and seeks to proactively put into place process or forum to enhance excellence in planning and execution across all studies in a phase• Follows established procedures and SOPs; seeks ways to improve and streamline processes to support the GCO CRO outsourcing model; provides feedback via appropriate channels for opportunities to improve processes or set best practices (i.e. PON)• Embodies a culture of continual improvement by seeking consistency and efficiency in processes and fully supporting the CRO partnership model• Is an advocate for the COL group and a visible contributor and vehicle to promote interaction• Is an influential leader and a resource for COLs within the Clinical Operations Management group.• Initiates and leads discussions at peer level forums relevant to the COL role and development in line with GCO best practices.• Able to influence MD on clinical study/program direction based on changing internal and external landscapes within phase, disease or therapeutic area; able to think strategically to best position a study within the current Clinical Development Plan.• Chairs SMT meetings and drives effective and efficient team operations through communication, goal setting and strategy implementation• Has a robust understanding of the study design including rationale, end points and patient population, and will ensure that the operational strategy supports both feasibility and scientific integrity• Develops and leverages Phase expertise (e.g.
Sr. Scientist/Principal Scientist, Translational Research and Clinical Biomarkers (Immunology) Antares TherapeuticsSr. Scientist/Principal Scientist, Translational Research and Clinical Biomarkers (Immunology)Boston, MA$160,000–$235,000 / yearCollaborate with teams across the organization, including clinical operations and data management, to ensure biomarker assay implementation and execution, and aid in the management of biomarker samples and data. The actual salary offered will be based on a number of factors, including but not limited to the qualifications of the applicant, years of relevant experience, level of education attained, certifications or other professional licenses held, and if applicable, the location in which the applicant lives and/or from which they will be performing the job.
NewAssociate Scientist - Neuroprotection And Resilience SanofiAssociate Scientist - Neuroprotection And ResilienceCambridge, MA$64.50–$93.17 / hourWe are looking for a highly qualified and motivated Associate Scientist to join the neuroprotection and resilience cluster in the Neurology Therapeutic Area for a one-year fixed contract, focused on discovering, validating, and developing therapies for neurodegenerative diseases including Alzheimer's, Parkinson's, and ALS. The successful candidate will have experience working in neurodegeneration in an academic or industry setting, with experience to perform cell culture-based experiments using iPSC cells and/or cell lines and supporting animal studies in models of brain disease.
Clinical Research Nurse National Health ServiceClinical Research NursePlymouth, England$32,073–$39,043 / yearThe Clinical Research Nurse / Practitioner will work as part of the clinical research team within the Emergency Department to support the safe conduct of research in in accordance with the Research Governance Framework and Good Clinical Practice guidelines and provide assurance that the rights, safety and well-being of trial participants are protected. Our team derives from a variety of backgrounds to create a multidisciplinary research team working together to deliver emergency care and front door research to a wide range of patients presenting to University Hospitals Plymouth NHS Trust from Plymouth and surrounding area.
Admin Contracts Assistant-Clinical Vendor Management Integrated Resources, IncAdmin Contracts Assistant-Clinical Vendor ManagementCambridge, MassachusettsContractorIndependent•Responsible for ensuring prompt and efficient receipt, signature, delivery, tracking, uploading and archival of all clinical contracts within the CVM group•Follows up on PO process from requisitions through to PO approval•Identifies areas for administrative process improvement and provides suggestionsWith Direction•Initiates purchase order requisitions upon receipt of supporting documentation as needed•May support Vendor Contract Manager in researching contract history and next available appendix informationMust have excellent communication skills, the ability to work efficiently and to perform tasks simultaneously with minimum supervision in a fast paced environment, exceptional organizational skills with a demonstrated ability to work in an accurate manner, great attention to detail, the ability to exercise sound judgment and determine priorities, the ability to work as part of a dynamic team, the ability to execute activities under tight timelines and high stress situations,proficiency with computers including MS Office suite with emphasis on Excel and Word, and the ability to quickly learn new technologies and processes. This may include collaborating with the Contracts Associate in providing oversight of CROs/FSPs who are contracted to upload contracts on our behalf to ensure commitments are met 20%•Data Cleanup and Migration: Collaborate with Contract Associates and Outsourcing Associate in the review and cleanup and migration of contract data in teams contract organizational tool and legal contract storage system.
Contracts Assistant Clinical Vendor Management Integrated Resources, IncContracts Assistant Clinical Vendor ManagementCambridge, MassachusettsFull timeDecision Making, Discretion & Latitude•Responsible for ensuring prompt and efficient receipt, signature, delivery, tracking, uploading and archival of all clinical contracts within the CVM group•Follows up on PO process from requisitions through to PO approval•Identifies areas for administrative process improvement and provides suggestionsWith Direction•Initiates purchase order requisitions upon receipt of supporting documentation as needed•May support Vendor Contract Manager in researching contract history and next available appendix informationKnowledge & SkillsMust have excellent communication skills, the ability to work efficiently and to perform tasks simultaneously with minimum supervision in a fast paced environment, exceptional organizational skills with a demonstrated ability to work in an accurate manner, great attention to detail, the ability to exercise sound judgment and determine priorities, the ability to work as part of a dynamic team, the ability to execute activities under tight timelines and high stress situations,proficiency with computers including MS Office suite with emphasis on Excel and Word, and the ability to quickly learn new technologies and processes. Job DescriptionPosition Details:Client Direct ClientLocation Lexington, MAJob Title Contracts Assistant Clinical Vendor ManagementDuration 7+ MonthsMust have skill-set [Job Description] Job SummaryTo work as an integral part of the Clinical Vendor Management (CVM) team providing proactive, high quality contracts administrative support to the global Vendor Contracts Managers (VCMs) in collaboration with the Contracts Associates.