• Platelet Biogenesis (Cambridge, MA)
    …The position calls for duties that are broad and variable, with significant opportunity for advancement. Specifically, you will be responsible for: Development and ... design of experiments for multiple projects within the Designer Platelet Team, with input from the CSO. Collaborate with project teams to optimize drug loading and delivery protocols and coordinate the characterization of drug-loaded platelets. Identify and… more
    Neuvoo (03/20/19)
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  • Radius Health (Waltham, MA)
    …include leadership of the team in predicting and planning solutions to achieve successful operational execution; driving the team to achieve clarity on issues and ... US-MA-Waltham Job ID 2019-1925 # of Openings 1 Category Clinical Ops - Dept Overview The Director of Project Management provides project leadership to cross-functional teams in the successful delivery of all phase drug development projects or sub projects… more
    Radius Health (03/19/19)
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  • Radius Health (Waltham, MA)
    …Provides strategic input to the clinical development plan Develops the operational plans for trials within the assigned development program(s) Oversees trial ... execution team to ensure delivery of clinical trial within budget and agreed upon timelines Identifies and/or anticipates operational risks and mitigation plans across trials within the development program and escalates issues to senior management as necessary… more
    Radius Health (03/08/19)
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  • Radius Health (Waltham, MA)
    …Key responsibilities include leading the development, scale-up, validation and registration of drug products and drug-device combination within the Radius portfolio, ... US-MA-Waltham | US-PA-Wayne Job ID 2019-1912 # of Openings 1 Category Pharmaceutical Development/Operations Overview Radius Health is searching for a Director, Drug Product Development, Tech Ops. with sound technical and leadership capabilities to develop our… more
    Radius Health (03/08/19)
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  • Radius Health (Waltham, MA)
    …Oversee investigational and post-marketing regulatory reporting and pharmacovigilance activities for assigned products. Medically review individual case safety ... reports from all sources for assigned products. Oversee, prepare, and review Periodic/Annual Reports (FDA) and Periodic Safety Update Reports and other Benefit/Risk Update Reports (FDA and Global Regulatory Authorities). Drive, prepare, and review responses to… more
    Radius Health (03/08/19)
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  • Radius Health (Waltham, MA)
    …Oversees and develops the Biometrics team; supervises hiring of team members and conduct development. Oversees input on design of study, reviews protocols, and ... US-MA-Waltham Job ID 2019-1908 # of Openings 1 Category Biometrics - Dept Overview The Senior Director Biostatistics oversee all the biostatistics, data management and programming tasks for Radius studies (nonclinical, CMC, clinical, safety, epidemiological or… more
    Radius Health (03/08/19)
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  • Radius Health (Waltham, MA)
    …Contributes to Global clinical / regulatory submissions (FDA, EMA, Canadian and other countries), by helping out with in house and site inspection readiness ... planning/training, Manages clinical study/studies according to global regulatory requirements. Leads cross functional study execution team to ensure goals and timelines are met. Manages and oversees CRO/Vendors to ensure compliance with processes and… more
    Radius Health (03/08/19)
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  • Radius Health (Waltham, MA)
    …Provide functional leadership for clinical operations, including hiring, training, staff assignments, coaching, mentoring and performance management in a matrix ... environment Set department goals and objectives which align with broader company goals Provide strategic and tactical input into integrated clinical development strategy and timelines Develop clinical operations strategy including risk management and… more
    Radius Health (03/08/19)
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  • Radius Health (Waltham, MA)
    …Assists in the implementation of GXP compliant procedures and operations to ensure a robust quality management system for both the conduct of clinical studies as well ... as prepare the company to successfully commercialize pharmaceutical products Proactively provides GCP QA support to Clinical Operations based on analysis and interpretation of updates to GCP regulations to assure best Clinical/QA practices Assists with the… more
    Radius Health (03/08/19)
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  • Unknown (Cambridge, MA)
    …What you will bring to this role: A PhD and post-doctoral training in a relevant scientific discipline plus a minimum of 4 years post-graduate experience. Some ... 6500! That's the number of associates in the Employer Institutes for BioMedical Research (NIBR). This division is the innovation engine of Employer, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for… more
    CMP Jobs (03/06/19)
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  • SimulStat's client (Marlborough, MA)
    …Work to create/maintain library of company metadata standards, including CRFs, Datasets, Variables, Value List, Controlled Terminology, Computation Method definitions ... in a single, easy to navigate repository that describes the data standards targets. Work to keep abreast of and incorporate new and updated data standards issued by CDISC and other Standards Development Organizations (SDO) which impact data processing… more
    Climber (03/16/19)
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  • DOCS (MA)
    …DOCS clients include small, mid and large sized Pharmaceutical companies in addition to many leading Biotechnology, Medical Device companies and CROs. As a global ... partner, DOCS currently offers global resourcing solutions to our clients. Roles & Responsibilities of the position W2 or 1099 preferred 5+ years of SAS experience working for a pharma or CRO CDISC experience (both SDTM and ADaM) BS acceptable, MS preferred… more
    Climber (03/15/19)
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  • DOCS (Boston, MA)
    …This role manages the outsourcing of clinical development projects to external service providers on behalf of Global Clinical Operations, allowing on-time, on budget ... and on quality delivery of clinical data to support the potential registration of new products. The role will require the use of advanced analytical skills to review complex clinical study assumptions and budget data and will require business knowledge of the… more
    Climber (03/15/19)
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  • Evidera (Waltham, MA)
    …: Define and refine research questions as they pertain to the SLR objectives Design of literature searches/algorithms to be implemented in scientific literature ... Senior Systematic Reviewer (Research Associate III) - Meta Research (Waltham MA or London UK)* * We are looking to fill this role in our Waltham, MA or London, UK offices The Team Do you have what it takes to conduct high-quality systematic literature reviews… more
    Neuvoo (03/20/19)
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  • CVS Health (Norwood, MA)
    …As a Pharmacy Technician I Sterile Compounding you will be working with cutting edge technology compounding specialized and complex therapies within the clean room ... environment. The Pharmacy Technician is essential to ensuring patients receive their medications in a timely manner. The Pharmacy Technician position is responsible for utilizing their clinical and IV/TPN knowledge alongside the pharmacist to provide specialty… more
    Neuvoo (03/19/19)
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  • Sterling Life Sciences (Boston, MA)
    …JOB DESCRIPTION Our client, a leading medical device company, is currently recruiting a Chief Financial Officer who will infuse the Finance Team with their talent, ... Sterling-Hoffman is a retained executive search firm that specializes in representing life sciences and technology companies in matters of high impact talent acquisition. Our clients include market leaders and venture capital-backed startups in industries such… more
    Sterling Life Sciences (03/21/19)
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  • FORMA THERAPEUTICS (Watertown, MA)
    …The Sr. Clinical Trial Manager will be responsible for independently managing multiple clinical trials of moderate to high complexity. The Sr. CTM will assume many ... critical activities including the management of internal and external stakeholders, ownership of the clinical trial strategy for execution, serving as a key participant in regulatory discussions and leading a high performing study team towards shared… more
    Neuvoo (03/14/19)
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  • FORMA THERAPEUTICS (Watertown, MA)
    …The Clinical Trial Manager (CTM) will be responsible for managing a broader range of activities on large multi-center studies as well as independent management of ... clinical trials of easy to moderate complexity. The CTM will assume many critical activities to support the Clinical Operations team to execute on clinical strategies to deliver successful operational outcomes across one or multiple clinical trials. Major… more
    Neuvoo (03/14/19)
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  • Cornerstone Search Group (Cambridge, MA)
    …Overall responsibility/leadership oversight of internal Clinical Operations staff, as well performance of CROs/external service providers. Provide strategic and ... tactical guidance in the planning, execution, and reporting in all operational aspects of the clinical trials. Perform gap analysis and develop processes and procedures for clinical trial conduct. Set clear goals, objectives, and milestones for Clinical… more
    Cornerstone Search Group (03/16/19)
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  • Unknown (Cambridge, MA)
    …will be to: Represent Biomarker Development on Respiratory and Ophthalmology Disease Area Decision Boards driving efforts to identify, develop, and drive disease, ... mechanistic biology, translational pharmacology and precision medicine biomarker approaches for the portfolio * Lead a matrixed group of biomarker subject matter experts and project team representatives to develop and oversee clinical project strategies, plans… more
    CMP Jobs (03/15/19)
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