Junior Clinical Project Manager job in London, England

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First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

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Job type: Permanent

Discipline: Program Manager / Director

Location: United Kingdom

This vacancy has now expired

An opportunity has opened for an experienced Junior Clinical Project Manager to work at an ambitious biotech company in London. This will be the perfect chance to develop your career.

Job Responsibilities

Create/Review patient consent forms and provide relevant opinion
Manage and support start up activities for UK, US and EU clinical trials sites including negotiation of contracts, site selection and review of essential regulatory documentation
Manage timeline adherence, site budget adherence in conjunction with the CPM and project quality deliverables
Interact with and day to day management of vendors including supporting CPM with vendor budget oversight
Manage contract requirements
Support in the recruitment and line management of CRAs as appropriate.
Perform occasional interim monitoring visits, including site qualification, initiation and close-out, including the source data verification of CRFs and Data clarification forms as stipulated
Co-ordinate the preparation and publication of data, reports and information, ensuring that these meet legislative, contractual and ethical requirements
To maintain Project documents in accordance with ICH-GCP and company SOPs and support the transition from paper to eTMF

Skills and Requirements

Strong clinical study experience in Oncology and or cell therapy.
Excellent collaboration and communication skills.
Adept at partnering with a diverse team and delivering results through taking ownership of key programme components.
Strong clinical, technical or disease area expertise. Knowledge of medical terminology and clinical patient management.
Minimum of 3-5 years UK clinical trial experience with minimum 2 years' experience in a senior or lead role
Previous experience of site monitoring in early phase oncology studies ideally in melanoma or NSCLC
Bachelor's degree (BSc, BA or RN equivalent) in biological or science-related field is essential

To Apply

In case you have difficulty in applying or if you have any questions, please contact Jack O'Neill at 0203 846 0646 or upload your CV on our website - www.proclinical.com/send-cv

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