Clinical Research Jobs in Maidenhead

The Head of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety regulatory affairs and medical affairs remain c...

Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations Good Clinical Practices (GCPs) ICH Guidelines AbbVie Standard Operating Pr...

MAIN PURPOSE OF JOBDefine and implement Area & Affiliate regulatory strategies & deliverables for a portfolio of compounds (early development late development marketed) for the Europe Region.Identify and advocate regions requirements in the overarching global regulatory strategy; develop risk assess...

About This Role:This entry-level Graduate position is an exciting opportunity to support the delivery of patient insight activities aimed at reducing protocol complexity and patient/site burden while advancing Patient Focused Drug Development (PFDD). As part of a dynamic team you will work closely w...

Job DescriptionProvides specialist medical/scientific strategic and operational input for one or a cluster of countries within Western Europe & Canada into core medical affairs activities such as: healthcare professional/provider interactions (Payers Patients Prescribers and Providers); generation o...

About This Role:The Senior Manager Feasibility is a member of the Feasibility Center of Excellence (FCoE) supporting data-driven study operational planning and protocol simplification accelerating study start-up activities and harmonizing processes to ensure study teams meet and exceed target progra...

London 23 days onsite (hybrid)Are you a regulatoryfocused Study StartUp expert who thrives on ownership and compliance Were looking for a Study StartUp PM to lead countrylevel submissions approvals and site readiness for a global clientdedicated program.What youll ownOversight of endtoend regulato...

About This Role:As the Senior Manager Global Regulatory Affairs you will join a dynamic team dedicated to navigating regulatory pathways at an above-market level. You will oversee the preparation submission and management of key regulatory submissions together with the EU Regulatory Lead ensuring co...

Advance AbbVies pipeline by striving for excellence in clinical research turning science into medicine for our patients and leveraging advanced capabilities to drive industry leading performance.Partners with study teams AbbVie internal R&D stakeholders investigators and site staff for meaningful an...

Job Overview:The Senior Director IT Finance isa strategic leadership role responsible for managing and optimizing the entire financial systems landscape and ensuring alignment with overall business objectives and regulatory requirements. This role manages the product backlog for Finance Treasury Pro...

PurposeDescribe the primary goals objectives or functions or outputs of this position.To advance AbbVies pipeline by striving for excellence in clinical research turning science into medicine for our patients and leveraging new capabilities to drive industry leading performance.This role is accounta...

Job DescriptionProvides specialist medical/scientific strategic and operational input for one or a cluster of countries within Western Europe & Canada into core medical affairs activities such as: healthcare professional/provider interactions (Payers Patients Prescribers and Providers); generation o...

In collaboration with line manager and/or Area Product Lead is responsible for implementation of registration strategy to ensure the regulatory approval of commercially successful pharma products in the Europe region. Is responsible for ensuring effective product maintenance and lifecycle management...

Work independently inform Line Manager;Acts as the primary Regulatory contact for identified therapeutic area of responsibility.Provides line management responsibility for a small team within UK Regulatory Affairs including recruitment goal setting performance appraisal and talent development.Overse...

Fortrea is currently seeking an In House CRA to join our multi-sponsor team in the this home-based youll play a key part in supporting global clinical trials across all phases working closely with Clinical Trial Leaders and cross-functional teams to ensure smooth trial delivery.Location: RemoteType...