Clinical Professionals Ltd

Senior Clinical Project Manager

Location
Cambridge
Posted
28 Jun 2019
Closes
28 Jul 2019
Ref
JO-1906-433169
Contact
Juber Rahman
Hours
Full Time
Contract Type
Permanent
Experience Level
Management

Senior Clinical Project Manager

Senior Clinical Project Manager Perm, Biotech, Great Abington

MUST HAVE: Ideally biotech experience but will consider pharma, Biologic or Oncology or Immunology or Autoimmune Disorder, hands-on experience with international exposure

Duration: Permanent
Salary: Very competitive, please contact me directly for this
Location: Great Abington

If you are looking for a change so you can work in a fun and friendly environment for a biotech organisation, why not apply for this role today?

Role

He/she will be responsible for operational delivery of one or more of the clients sponsored clinical trials.
Main Responsibilities

- To lead the clinical trial team (internal and external) tasked with delivery of a companys sponsored clinical trial
- To assist in the selection of appropriate vendors for the conduct of companys sponsored clinical trials
- To work with vendors to define operational details of companys sponsored clinical trials
- To develop study management plans ensuring sponsor oversight of clinical trials in accordance with companys procedures
- To review vendor generated clinical trial related documents to ensure compliance with the objectives of the trial, companys procedures and relevant standards
- To act as the key contact for trial associated vendors and ensure timely and effective communication between involved parties
- To ensure essential documents allowing the reconstruction of each trial are generated, filed and maintained by or on behalf of company
- To manage trial budgets and track trial related payments to vendors
- To communicate progress and identify risks and issues arising on clinical trials to the VP Clinical Operations and other company development team members as appropriate
- To maintain awareness of, and ensure compliance with, company policies and procedures relating to quality standards within the Company

Skills/Requirements

- Degree level education or nursing or other healthcare professional equivalent
- Substantial experience of managing outsourced clinical trials
- Ideally looking for someone with experience in the biotech industry
- Hands-on experience, day-to-day management of sponsored clinical trials
- Experience in clinical trials across a range of therapeutic areas and geographic (UK, EU & US), strongly preferred would be biological; experience of oncology would also be advantageous
- Robust knowledge of GCP and related regulatory guidelines governing clinical trials in the UK, EU & USA
- Influencer with ability to work in a flexible, collaborative style with colleagues and teams within the company and with external advisors including CROs and consultants
- Excellent matrix management skills and ability to manage contractors and collaborators
- Ability to see complex projects to completion, and to work on a broad range of tasks within a project

Not ready to apply or have some questions first? No problem, please feel free to contact me, Juber Rahman at any time on +44 (0) 207 822 1710 / juber.rahman@clinicalprofessionals.eu

If this role is not suited to your skillset, please feel free to share these details within your professional networks as we do offer a generous bonus referral scheme of 250 in vouchers should we go on to successfully please someone you recommend to us.

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