Head of Clinical Trial Delivery - Cambridge

This role plays a pivotal part in the Leadership Team for Quantitative Sciences & Development Operations (QSDO). The Head of Clinical Trial Delivery will lead clinical trial delivery across all Biogen Disease Areas. · About This Role: · You will have broad responsibility for a di ...

This role involves leading clinical trial delivery across all Biogen Disease Areas, taking broad responsibility for a diverse portfolio of clinical programs in Neuroscience, Rare Disease, and MS/Immunology therapeutic areas. · Oversee clinical trial delivery for Neuroscience, Rar ...

This job is with Biogen. As the Head of Clinical Trial Delivery, you will play a pivotal role in the Leadership Team for Quantitative Sciences & Development Operations (QSDO). The base compensation range for this role is: $342,000.00-$496,000.00 ...

The Head of Clinical Trial Delivery will play a pivotal role in the Leadership Team for Quantitative Sciences & Development Operations (QSDO) at Biogen. This individual will lead clinical trial delivery across all Biogen Disease Areas and provide strategic operational leadership ...

About This Role: · As the Head of Clinical Trial Delivery, you will play a pivotal role in the Leadership Team for Quantitative Sciences & Development Operations (QSDO). You will lead the charge in clinical trial delivery across all Biogen Disease Areas, taking broad responsibili ...

The Clinical Trial Leader Director serves as the day-to-day operational owner for specific RLT clinical trials. · ...

· Manage all project team activities related study start up, conduct and close out activities. · Work with Outsourcing and Contracts Management to ensure Site Contracts reflect trial activities and related budget. · ...

We are seeking an experienced and highly motivated Director / Senior Director of Clinical Operations to lead the operational execution of the Company's first clinical program in Type 1 diabetes as it advances into early-phase clinical trials. · Lead clinical operations strategy a ...

The Manager Clinical Operations is responsible for the execution of study-level activities. · Manage integration of project team activities. · Provide input on trial level operational strategies for clinical trials. · ...

· Company Overview · Fulcrum Therapeutics, Inc. ("Fulcrum") [NASDAQ: FULC] is a clinical-stage biopharmaceutical company focused on developing small molecules to improve the lives of patients with genetically defined rare diseases in areas of high unmet medical need. Fulcrum's l ...

· At Editas Medicine, we are pioneering the possible. Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world.  Our ...

We are collaborative and united by a common mission to create transformative genetic medicines for prevalent diseases. · - Plan, drive and oversee all aspects of multi-center global clinical trials in compliance with GCPs, SOPs, and within designated program budgets and timelines ...

We are seeking a Clinical Data Validation Engineer to contribute to groundbreaking advancements in a remote setting. This role offers the opportunity to leverage your data management and programming expertise, specifically with the Elluminate platform, to support critical project ...

We seek a highly motivated and experienced Clinical Site Relationship Specialist for clinical trials. · To build strong relationships with site investigators, study teams, and other key stakeholders involved in clinical trials. · Assist in building and managing clinical site rela ...

The Clinical Study Associate Manager (CSAM) Service supports the Clinical Study Lead by taking responsibility for areas of clinical trial delivery. · ...

· Company Description · Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on ...

+Job summary · The Vice President, Compliance is responsible for designing and implementing the company's Corporate Compliance Program to oversee promotional materials and HCP/patient programs.+ResponsibilitiesResponsible for Clinical Supplies Planning and Forecasting as required ...

· Responsible for the statistical strategy for one or more clinical programs/studies and providing oversight of CRO biometrics deliverablesSupport clinical development team to enable robust study design and execution with a focus on innovative and efficient quantitative decision ...

Seeking an experienced Project Manager with basic knowledge of Digital Health. · Support the Clinical Device Solutions team with high level time-keeping and note taking. · Creation of dashboards/visualization/slides and action items follow up. · Direct ownership on small-medium ...

The Vice President, Compliance is responsible for designing and implementing the company's Corporate Compliance Program to ensure integrity and compliance with all applicable laws, regulations, and internal policies. · ...