European SCPM – Remote Based, Devices, Freelance, Needed Now!

European SCPM - Remote Based, Devices, Freelance, Needed Now!

Job Type: permanent
Salary: competitive
Posted: 11th December 2019
Ref: JLSMSCPM2020

I am currently partnered with a Device company based overseas. This company is looking to expand their business into Europe in the coming months of 2020.

My client currently has 2 x Phase I studies and is looking to progress further.They are know looking for the correct person to perform oversight of the CRO to ensure the best results possible are achieved.

With an outstanding team of 6, you will be involved with a very tight and well organised team. There will be an expectation to hit the ground running and assist the team when required.

With most freelance/consulting positions you will not be given the opportunity to become such a big part of the team, however they have requested that this person will play a big part in the team and have a future with the company.

You will be given 2 weeks for a hand over by the current Project Manager, before they go on parental leave.

 

Responsibilities:

(Will include but not limited to)

  • Formulation of Device protocols and related documentation in collaboration with the Clinical Team.
  • Lead and matrix manage the global multidisciplinary COT to ensure all trial deliverables are met according to timelines, budget, quality standards and operational procedures
  • Identify sites and manage study set-up
  • Lead the clinical trial protocol development process
  • Responsible for ordering and management of clinical trial materials
  • Support the CRA on study related questions and serve as point of contact for managing/ answering questions relating to trial procedures and subjects eligibility
  • Responsible for set up and maintenance of the Trial Master File for assigned studies
  • Regularly update all trial information databases in order to manage accuracy of information
  • Approve for all necessary center payments
  • Co-ordinate pre-audit activities for nominated projects
  • Contribute to identification and evaluation of new centers suitable for performing TM studies in healthy volunteer and patients.
  • Extensive experience in an oversight role

Requirements:

(As a minimum)

  • 5 years of experience as a Project Manager
  • 5 years of experience as a Freelancer/Consultant
  • 5 years Biotech experience
  • Extensive oversight experience
  • Life Science Degree
  • Motivates staff and ensures team effectiveness through eliciting feedback
  • Excellent communication, presentation and problem solving skills.
  • Previous experience in the management/coaching of direct reports.

If this position is for you, or you are eager to find out more then do not hesitate to get in touch with me directly for a conversation on the below:

Jlambert@barringtonjames.com

Telephone: +44 1293 776644

Or on LinkedIn Directly

 

Get Applying…

About Your Consultant

Email: jlambert@barringtonjames.com Telephone: 01293776644

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