Research Associate Co-Op, Kidney Fibrosis Keros TherapeuticsResearch Associate Co-Op, Kidney FibrosisLexington, MA$28–$32 / hourWith a focus on developing differentiated product candidates that are designed to alter TGF- signaling, we aim to target the pathways critical for the growth, repair and maintenance of blood cells and a number of tissues, including bone, skeletal muscle, adipose and heart tissue. Any resume submitted by an agency without a signed contract or expressed consent by a member of the Keros Therapeutics Human Resources Department, will be considered property of Keros Therapeutics, and no fee shall be owed with respect thereto.
Health Economics & Outcomes Research Associate Director, Pain Vertex PharmaceuticalsHealth Economics & Outcomes Research Associate Director, PainBoston, Massachusetts$176,000–$264,000 / yearLeads others to execute complex HEOR evidence generation including, cost-effective analysis and budget impact models, prospective and retrospective observational studies, ITCs, meta-analyses and systematic reviews, patient reported outcomes measure development and validation and other research as needed to support the asset value. We seek talent who bring an external perspective, demonstrate curiosity and sound judgment, and thoughtfully adopt new capabilities that improve decision-making, drive innovation, increase efficiency, and help deliver better outcomes for patients.
Research Associate Co-Op, In Vitro Pharmacology Keros TherapeuticsResearch Associate Co-Op, In Vitro PharmacologyLexington, MA$28–$32 / hourWith a focus on developing differentiated product candidates that are designed to alter TGF- signaling, we aim to target the pathways critical for the growth, repair and maintenance of blood cells and a number of tissues, including bone, skeletal muscle, adipose and heart tissue. Any resume submitted by an agency without a signed contract or expressed consent by a member of the Keros Therapeutics Human Resources Department, will be considered property of Keros Therapeutics, and no fee shall be owed with respect thereto.
Research Associate Spear BioResearch AssociateWoburn, MassachusettsStrong presentation and interpersonal skills with the capability to establish collaborative working relationships and become a key contributor within the assay development, platform and product teams. BS in Biology, Biochemistry, Biomedical Engineering or a related discipline plus minimum 2-3+ years in an academic or industry lab, or MS degree with 1-2+ years of related experience.
Research Associate II In Vivo Pharmacology CbResearch Associate II In Vivo PharmacologyLexington, Massachusetts$48,000–$60,000 / yearThe successful candidate will have hands-on experience conducting rodent studies in a CRO, biotechnology, or pharmaceutical environment and will be responsible for study execution, animal procedures, sample collection, and data documentation. This position works closely with study scientists and project teams to ensure high-quality study conduct, adherence to timelines, and compliance with animal welfare and regulatory requirements.
Research Associate Co-Op, Bioanalytical Keros TherapeuticsResearch Associate Co-Op, BioanalyticalLexington, MA$28–$32 / hourWith a focus on developing differentiated product candidates that are designed to alter TGF- signaling, we aim to target the pathways critical for the growth, repair and maintenance of blood cells and a number of tissues, including bone, skeletal muscle, adipose and heart tissue. Any resume submitted by an agency without a signed contract or expressed consent by a member of the Keros Therapeutics Human Resources Department, will be considered property of Keros Therapeutics, and no fee shall be owed with respect thereto.
Clinical Operations Associate I (College Grad 2027) SolaceClinical Operations Associate I (College Grad 2027)Boston, MassachusettsSolace cuts through the red tape of healthcare by pairing patients with expert advocates and giving them the tools to make better decisions—and get better outcomes. Clinical or healthcare interest is a significant plus—it'll help you understand context faster and build better systems, but we care more about operational chops than clinical credentials.
Primary Market Research Junior Associate RA Capital ManagementPrimary Market Research Junior AssociateBoston, Massachusetts$60,000–$80,000 / yearFrom helping them recruit talent to helping them recruit patients for their studies to helping match them to strategic partners and even going to Washington to win reforms, RA Capital’s large team has people with nearly every relevant expertise one might need to turn an idea into a cure that actually helps people. This role is ideal for someone with approximately 2 years of experience in life sciences consulting, pharmaceutical market research, or a related healthcare research role who has hands-on experience designing and executing primary research studies.
Clinical Trial Associate CRISPR Therapeutics AGClinical Trial AssociateSouth Boston, MA$85,000–$95,000 / yearThe Company has evolved from a pioneering research-stage organization into an industry leader, marking a historic milestone with the approval of CASGEVY (exagamglogene autotemcel [exa-cel]), the world's first CRISPR-based therapy, approved for eligible patients with sickle cell disease and transfusion-dependent beta thalassemia. The Company continues to expand its leadership in gene editing through the development of SyNTase editing, a novel and proprietary gene-editing platform designed to enable precise, efficient, and scalable gene correction.
Associate Director Clinical Data Management ModeX Therapeutics IncAssociate Director Clinical Data ManagementWESTON, MATrack project progress and issue status reports to ensure the achievement of key Data Management milestones, such as database Go-Live and completion of tasks towards Database Lock. Develop or assist with the project training development and delivery, for investigators, clinical sites, project teams and CRO on data collection processes, tools and/or equipment as required.
NewAssociate Director, Clinical Sciences Hemab ApSAssociate Director, Clinical SciencesCambridge, MAAs Associate Director, Clinical Sciences, youll help translate Hemabs science into well-designed clinical studies and reliable evidence about how our treatments perform in patients. Youll be joining at a stage where individual decisions still carry real weight, and where your work can help turn promising science into a preventative treatment that actually reaches patients.
Associate Director, Clinical Program Quality and Excellence (Oncology) 3316 Takeda Development Center AmericasAssociate Director, Clinical Program Quality and Excellence (Oncology)MassachusettsProvides quality assurance oversight of the global clinical research programs in Research and Development (R&D), Plasma Derived Therapy (PDT), Vaccines Business Unit (VBU), Oncology Business Unit (OBU) and Global Medical Marketed Products Development (MPD) with the overall goal of inspection readiness. Lead investigations into significant quality issues, scientific misconduct and serious breach of GCP; facilitate identification of root cause and development of appropriate corrective and preventive actions; track actions and confirm effectiveness; ensure reporting of potential or confirmed violations to regulatory authorities.
Associate Director Clinical Scientist, Immunology Cell Therapy AstraZeneca PlcAssociate Director Clinical Scientist, Immunology Cell TherapyCambridge, MA$142,171.20–$213,256.80 / yearStudy level: Serving as the clinical science resource for assigned studies (and in some instances as the Study Clinical Lead); supporting/leading development of Clinical Study Protocols (CSPs), informed consent forms (ICFs), and electronic data capture (EDC) database specifications in line with the approved CDP and target product profile; supporting ongoing clinical data review and interpretation at study and program level with input from the study/program physician; contributing to development of quality metrics and data review plans for assigned studies; support and contribute to medical monitoring of trials; supporting the compilation and interpretation of data for dose‑escalation/safety review committees; supporting protocol amendments and other strategic documents; and supporting review of the Clinical Study Report. ESCR and external engagement: Co‑leading/supporting ESCR strategy and implementation for the program; serving as the interface between the GPT and external clinical research; supporting investigator/site relationships for site selection and study start‑up; co‑leading/supporting clinical proposal reviews, protocol reviews and scientific oversight for academic basket/umbrella and ESCR studies; identifying and managing ESCR portfolio risks and escalating quality issues through appropriate channels; supporting representation of the project internally and externally with key experts and partners and contributing to alliance development.
Associate Director Clinical Scientist Immunology Cell Therapy AstraZeneca PlcAssociate Director Clinical Scientist Immunology Cell TherapyCambridge, MA$142,171.20–$213,256.80 / yearStudy level: Serving as the clinical science resource for assigned studies (and in some instances as the Study Clinical Lead); supporting/leading development of Clinical Study Protocols (CSPs), informed consent forms (ICFs), and electronic data capture (EDC) database specifications in line with the approved CDP and target product profile; supporting ongoing clinical data review and interpretation at study and program level with input from the study/program physician; contributing to development of quality metrics and data review plans for assigned studies; support and contribute to medical monitoring of trials; supporting the compilation and interpretation of data for dose‑escalation/safety review committees; supporting protocol amendments and other strategic documents; and supporting review of the Clinical Study Report. ESCR and external engagement: Co‑leading/supporting ESCR strategy and implementation for the program; serving as the interface between the GPT and external clinical research; supporting investigator/site relationships for site selection and study start‑up; co‑leading/supporting clinical proposal reviews, protocol reviews and scientific oversight for academic basket/umbrella and ESCR studies; identifying and managing ESCR portfolio risks and escalating quality issues through appropriate channels; supporting representation of the project internally and externally with key experts and partners and contributing to alliance development.
Associate Director, Clinical Data Programmer Amylyx PharmaceuticalsAssociate Director, Clinical Data ProgrammerCambridge, MARemote$188,000–$211,000 / yearThis individual will work collaboratively cross-functionally to provide hands-on data management support, programming support and technical leadership to develop, maintain, validate the clinical database, and run computer programs that access, visualize, and report clinical trial data, in accordance with various clinical plans, ICH guidelines, and applicable regulatory requirements. You will be expected to travel to our corporate location in Cambridge, MA several times a year and attend other company-related events as necessary and requested, which may include travel by air, driving or public transportation.
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.
Associate Director, Clinical Data Management X4 Pharmaceuticals IncAssociate Director, Clinical Data ManagementBoston, MAThe Associate Director will oversee CRO partners and vendors, drive data quality and inspection readiness, support regulatory submissions, and ensure the timely delivery of high-quality clinical trial data. Does it excite you to be a part of a patient-focused company developing potential new treatments that could dramatically improve the lives of patients with limited to no current treatment options?
Research Associate Spear Bio IncResearch AssociateWoburn, MAStrong presentation and interpersonal skills with the capability to establish collaborative working relationships and become a key contributor within the assay development, platform and product teams. Qualifications: BS in Biology, Biochemistry, Biomedical Engineering or a related discipline plus minimum 2-3+ years in an academic or industry lab, or MS degree with 1-2+ years of related experience.
NewAssociate Director, Clinical Operations (Contract) Centessa Pharmaceuticals, LLCAssociate Director, Clinical Operations (Contract)Boston, MA$75–$110 / hourCentessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders. Centessa's OX2R agonist portfolio includes additional clinical and preclinical-stage assets with potential utility across a broader range of neurological, neurodegenerative, and neuropsychiatric conditions.
Research Support Specialist Mass General BrighamResearch Support SpecialistSomerville, Massachusetts$17.71–$24.28 / hourThe Center provides a range of clinical services to women, which include: consultation regarding the use of psychiatric medications during pregnancy; treatment for postpartum mood and anxiety disorders; treatment for premenstrual syndrome; and treatment of menopause-related mood and anxiety symptoms, sleep disorders, and hot flashes. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success.