- Actalent (Cambridge, MA)
- As a Senior Manager Clinical Study Lead... study team responsible for the delivery of clinical studies and research collaborations. You will ... study systems. Responsibilities + Lead the cross-functional study team for clinical study ...Ensure accurate budget management and address scope changes for studies . + Escalate issues related to study … more
- Takeda Pharmaceuticals (Boston, MA)
- …to bring life-changing therapies to patients worldwide. **_Objective / Purpose:_** The Senior Manager , Clinical Partner Outsourcing (CPO) ensures seamless ... and policies. + Lead ballparking, contracting and commercial management of complex clinical studies , understanding study requirements and translating into… more
- IQVIA (Boston, MA)
- …Clinical Data Management role. + Your previous roles/job titles may include _Clinical Data Manager , Senior Clinical Data Manager , Lead Data Manager ... now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to...You'll Do** + Lead data management for complex, global clinical trials from study setup to database… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …and investigator registrations, clinical trials education, and committee management. The Clinical Trials Education Manager reports to the Director of ODQ. ... The Clinical Trials Education Manager is responsible for supervising and overseeing...Reporting metrics and statistics to the ODQ Director and senior DF/HCC leadership + Oversee the development, review, and… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …company that will inspire you and empower you to shine? Join us as a Clinical FP&A, Manager in our Cambridge, MA office. At Takeda, we are transforming ... + Independently leads financial planning, analysis, and reporting for clinical trial costs. + Actively contributes to functional and...+ Act as a trusted finance business partner to study team, and build an environment to both challenge… more
- ConvaTec (Lexington, MA)
- …and Convatec's policies and SOPs. **Key Responsibilities:** + Working closely with Clinical Study Managers (CSMs) and Clinical Research Associates ... Clinical Research Organizations (CROs) and other vendors for clinical studies that are outsourced to third...documents such as the protocol, investigator brochure, regulatory documents, clinical study reports and other documents and… more
- Dana-Farber Cancer Institute (Boston, MA)
- The Clinical Research Project Manager II manages day-to-day coordination and overall clinical trial activities for the Psychedelic-Assisted Therapy (PAT) ... therapies for individuals with advanced cancer and serious illness. The Clinical Research Project Manager II oversees trial startup coordination,… more
- Bristol Myers Squibb (Cambridge, MA)
- …and execution of multiple clinical trials (eg significant experience as a senior clinical leader), and exhibits all of the following attributes: + Able ... and achieve results through teams, and is the direct manager to Clinical Trial Physicians (CTPs) **Key...studies , with the support of the CTPs and Clinical Scientists (CS) within the asset and/or indication +… more
- Pfizer (Cambridge, MA)
- …informed consent documents, and contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other clinical ... for programs within the Late-Stage Oncology portfolio. **KEY RESPONSIBILITIES** + Clinical development expert for assigned studies maintaining current scientific… more
- Tufts Medicine (Boston, MA)
- …up of multiple Principal Investigators, a senior clinical coordinator, and a clinical studies manager , who enjoy the day-to-day work of discovery and ... assist the Principal Investigator (PI) in planning and implementing clinical research studies as assigned. Our team...regulatory binders, case report forms, source documents, and other study documents. Monitors the occurrence of clinical … more
- Parexel (Boston, MA)
- …for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international ... **CRA and Sr CRA positions- Remote - Need for SE...escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance… more
- RELX INC (Cambridge, MA)
- …healthcare to partner for a better world. About the Role We are seeking a Sr Manager Segment Strategy to develop and embed audience segmentation and go-to-market ... health education and interactive learning, as well as exceptional healthcare and clinical practice. At Elsevier, your work contributes to the world's grand… more
- Beth Israel Lahey Health (Boston, MA)
- …recruiting, screening and enrolling of patients for participation in multiple clinical trials, ensuring compliance with federal, state and institutional guidelines. ... protocols; supervising, planning and prioritizing the work of the Clinical Research Coordinators. **Job Description:** **Essential Responsibilities:** + Participates… more
- Oracle (Boston, MA)
- …Manager , ShiftAlert, Demand Manager , Outcomes-Driven Acuity, and Patient Progress Manager . **Responsibilities** As a Senior Clinical Consultant, you ... **Job Description** As a Senior Clinical Consultant, you will collaborate...related work experience including: + Bachelor's degree in Nursing, Clinical Studies , Health Care, or related field… more
- Dana-Farber Cancer Institute (Brookline, MA)
- **This is Part-Time; 24 hours/week role** Under direct supervision of the Senior Clinical Research Accounts Specialist, the Clinical Research Accounting ... to higher -level staff. In the absence of a Senior Clinical Research Accounts Specialist this position...studies and funding sources, as applicable. + Monitors study payment activity and consistently pursues collections from extramural… more
- Parexel (Boston, MA)
- **Job Purpose:** The Senior Clinical Research Associate ( Sr . CRA) is responsible for the site management, site monitoring and close-out of assigned ... Study Operations Manager (SOM) + When required Partners with other Study Team members (eg Clinician, Recruitment Specialist, Clinical Data Scientist) +… more
- Sanofi Group (Cambridge, MA)
- …is to: + Provide medical expertise in the Study team to conduct the clinical studies from early phases to LCM programs + Collaborate with other medical and ... **Job Title:** Senior Clinical Research Director **Location:** Cambridge,...medical input & support for all activities related to clinical studies conduct such as answers to… more
- Parexel (Boston, MA)
- The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in ... for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international… more
- Takeda Pharmaceuticals (Boston, MA)
- …company to inspire you and empower you to shine? Join us as a Senior Manager , Feasibility based remotely reporting to the Director, Feasibility. At Takeda, ... + Conduct data-driven feasibility assessments for Phase I - IV clinical studies , including protocol design optimization, country/site feasibility and… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …innovation-driven company that will inspire you and empower you to shine? Join us as a Senior Manager of Statistics- CMC in our Cambridge, MA office. As a ... Senior Manager of Statistics, you will provide...analysis, and interpretation of Chemicals, Manufacturing, and Controls (CMC) study data throughout Pharmaceutical Sciences. We seek an innovative… more