Project Manager in United Kingdom

Avania are hiring – Project Manager

As the Project Manager, you will have the opportunity to provide leadership through planning, organizing and overseeing all clinical trial activities and deliverables from study start-up to close out. The Project Manager is responsible for implementing and managing the project planning; tracking of the clinical monitoring process; and administration and overview of clinical trials. The position requires a proactive role in developing the project planning and monitoring of both resources and clinical trial so that all aspects of the plan can progress effectively.

The Project Manager will:

• Supervise the Project Team to ensure trial deliverables are on time, within budget and in appropriate quality, in compliance with applicable SOPs, ISO14155 / ICH-GCP and all applicable (local) regulations

• Manage the project planning and tracking of trial progress of various international clinical trials from start-up to close out

The role of Project Manager also has financial responsibilities, and you will:

• Maintain and perform regular budget reviews for your allocated studies

• Assist the Management Team in preparing budgets and forecasts as required and possibly have involvement in bid defense meetings

Since Quality is in our DNA, a key responsibility of the Senior Project Manager role is to keep our quality standards high for our clients

Please note, The Project Manager role can be hired in either UK, Netherlands, Spain or Germany

Candidates who offer a combination of the skills, knowledge and experience listed below are encouraged to apply to Avania’s Project Manager role. With our continued growth we are hiring talent to join us on our journey and grow with us.

Please note, The Project Manager role can be hired in either UK, Netherlands, Spain or Germany

We ask

• Relevant degree in (para)medical life science or nursing preferred.

• GCP-ICH-E6, FDA regulations and ISO 14155,13485 and 9001 knowledge where applicable

• Knowledge of regulatory regulations and guidelines on medical devices

• Proficient in the use of computer and software systems (Microsoft Word, Excel, PowerPoint, email)

• 5 years’ experience in clinical trials

• Ability to travel domestically and internationally

• Fluent in spoken and written English, with excellent communications and interpersonal skills

We offer

• The opportunity to work in an innovative, fast-growing and rewarding industry

• A dynamic and enthusiastic global team that fosters collaboration and the opportunity to work with experts across many specialties

• Exchange of knowledge and ideas to help employees grow and advance their careers, backed with training and other development opportunities

• Competitive compensation and benefits package (details shared during the interview process)

• Some roles offer the opportunities for travel

• Ask us about our hybrid and fully remote work opportunities

We look forward to receiving your application!

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