Clinical Trials Manager

At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the worlds biggest health challenges and our mission requires collaboration determination and a relentless drive to make a difference.

Every member of Gileads team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions and were looking for the next wave of passionate and ambitious people ready to make a direct impact.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future you are the key driver in evolving our culture and creating an environment where every employee feels included developed and empowered to fulfil their aspirations. Join Gilead and help create possible together.

Job Description

FUNCTION:

Clinical Operations

POSITION OVERVIEW:

Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all Gilead therapeutic areas. Clinical Operations plays a key role in ensuring all Gilead clinical trials are performed in accordance with applicable SOPs company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of Gileads products.

In this Clinical Trial Manager (CTM) role you will manage a geographical region(s) or multiple components of PostAuthorization NonInterventional Studies (NIS) required to fulfil regulatory commitments (PASS PAES PMRs) safety obligations and evidence needs for regulatory filings. You will define and incorporate study logistics and study plans to accomplish clinical study objectives. You may also participate in strategic initiatives / projects.

The role will be located in the Gilead European offices in London.

EXAMPLE RESPONSIBILITIES:

• Manages a geographical region(s) of assigned clinical studies or multiple components of larger studies.
• Collaborates with other functions on how to best achieve study goals and objectives and communicates cross-functionally to ensure project team goals are met.
• With guidance may overseas and/or manage interactions and deliverables from relevant CROs subcontractors and vendors.
• Typically serves as the key operational contact for Gilead studies providing oversight for the site evaluation initiation and close-out visits in addition to oversight CRO conducted monitoring visits.
• Defines study logistics and overseas develops clinical study plans for assigned clinical studies.
• Manages study timelines including documentation and communications.
• Provides input into study protocols case report forms and informed consents oversees/authors study plans and presentations.
• Provides oversight of study sites/region and reviews routine regulatory documents to ensure that CROs /vendors are in compliance with protocols regulatory requirements SOPs and monitoring plans.
• Leads or otherwise assists in the preparation of safety interim and final study reports including resolving any data discrepancies.
• Proactively identifies potential operational challenges and collaborates with other Clinical Operations colleagues to provide solutions to ensure study execution remains on track to defined protocols budgets and timelines.
• Participates and/or acts as a Business Lead in initiatives / projects and manages project meetings and conference calls with CROs other vendors and cross-functional teams as appropriate.
• Contributes to SOP development and/or participates in special projects. Develops tools and processes that optimize project efficiencies and effectiveness.
• Assists in training new or less experienced colleagues.
• Ensures own work complies with established practices policies and processes and any regulatory or other requirements.

REQUIREMENTS:

We are all different yet we all use our unique contributions to serve patients. Please see the following for the qualifications and skills we seek for this role.

Minimum Education & Experience

• MA / MS / PharmD / PhD with 3 years relevant clinical experience in life sciences or BA / BS / RN with 5 years relevant clinical experience in life sciences.
• Minimum of 2 years of Post-Authorization Non-Interventional study management experience at international level.
• Experience in managing sites activities as study coordinator or in oversight site activities as Clinical Research Associate (CRA).
• Experience in working with cross-functional stakeholders as Medical Affairs and Real Word Evidence/Epidemiologist teams.

Knowledge & Other Requirements

• Demonstrated ability to be a fast learner.
• Demonstrated ability to be flexible and adaptable to change to move between projects easily and provide support/expertise where needed.
• Ability to manage any component of full cycle study management from start-up to close-out.
• Advanced knowledge of study management best practices and tools and has shown ability to apply these to improve study efficiencies and effectiveness.
• Fully understands protocol requirements and effectively articulates and interprets these.
• Knowledge of Food & Drug Administration (FDA) European Medicines Agency (EMA) and other applicable national regulations International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines and Good Clinical Practice (GCP) governing the conduct of clinical studies.
• In deep knowledge of Good Pharmacovigilance Practice (GVP) and related key modules as well as FDA RWE guidances.
• Familiar with standard medical / scientific terminology.
• Ability to communicate in a clear and concise manner.
• Ability to support a team-oriented highly-matrixed environment.
• Ability to execute multiple tasks as assigned.
• When needed ability to travel.

Equal Employment Opportunity (EEO)

It is the policy of Gilead Sciences Inc. and its subsidiaries and affiliates (collectively Gilead or the Company) to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law all employment actions relating to issues such as compensation benefits transfers layoffs returns from layoffs company-sponsored training education assistance social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds which may include an individuals gender race color national origin ancestry religion creed physical or mental disability marital status sexual orientation medical condition veteran status and age unless such protection is prohibited by federal state municipal provincial local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.

For Current Gilead Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.

Required Experience:

Manager

Employment Type : Full-Time
Experience: years
Vacancy: 1