Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms RSS Feed RSS Feeds RSS Feed PharmiWeb Candidate Blog RSS Feed PharmiWeb Client Blog

Job Details

Top Global Pharma seeks ePRO Project Manager/ permanent/ Buckinghamshire

Company: DOCS Global
Location: Buckinghamshire
Reference: Ref AS-019788
Closing Date: 29 Dec 16
Type: Full Time
Salary (£): Competitive
Benefits: Excellent & Comprehensive

Job Summary:

Exciting opportunity to work for a Top Global Pharma, the TOP 30 companies to work for (As listed on the Sunday Times 2016). Our client is now seeking an experienced Project Manager in ePRO Systems to work within their team as a Clinical Technology Services Manager, ePRO. The role is office based in Buckinghamshire with flexibility of working from home 2 days a week! The role is permanent through DOCS and contracted to our client long term/indefinate.


Roles & Responsibilities of the position

  • Provide advice/recommendation to study teams regarding the supplier(s) and device/technology alternatives
  • Complete Requests for Proposal documentation, and recommend appropriate suppliers to support study needs
  • Provide leadership and expertise for the completion of supplier specification development and set-up activities through lifecycle of the trial
  • For all protocol-dictated PROs and ClinROs: research copyright & language availability, ensure permission/licensing, obtain required study translations (requires working with
  • preferred translations vendors) according to the FDA’s PRO Guidance
  • Lead the cross functional study team through changes of scope for ePRO/pPRO (including ClinROs), providing technical expertise on the change of scope, assessment of risk, oversight of system requirements updates and user acceptance testing
  • Lead the resolution of issues escalated by study teams as well as cross-team specific issues under the supervision of the Director or Associate Director, Clinical Technology Services
  • Serve as the point of contact specific to inspection readiness activities between the study team and the ePRO/pPRO supplier (s)
  • Effectively manage internal and external business partner relationships in support of R&D Operations’ deliverables
  • Monitor key performance indicators (KPIs) for services provided by suppliers
  • Conduct Lessons Learned sessions following the completion of study start-up activities, and, as necessary, throughout other phases of the clinical development process
  • Effectively support the study team in close-out/deactivation of the ePRO system
  • Provide leadership for supplier assessment/qualification teams
  • Continually assess new emerging technologies to optimize operational efficiencies
  • Represent Clinical Technology Services as an ePRO/pPRO subject matter expert at internal cross-company meetings and at external professional meetings
  • Healthcare Compliance and Ethical Code of Conduct of Pharmaceutical Medicine

Job Requirements

  • Bachelor’s degree (University degree) or equivalent education required
  • Very strong operational experience in clinical trials with a pharmaceutical company and/or a Clinical Research Organization is required
  • Demonstrated knowledge of clinical development processes, global clinical operations, and strategic planning is required
  • Familiarity with industry best practices for vendor management is required.
  • Good understanding of the therapeutic areas
  • Experience with ePRO/pPRO systems or suppliers is a must
  • Strong project management skills and presentation skills with the ability to lead a team independently
  • Our client would consider a Clinical Data Manager at Project Management level who has recently worked on ePRO systems OR a strong Clinical Project/Trial Manager who has used ePRO systems and have a strong understanding of this. 

Remuneration & other details

• Base salary
• Car Allowance of £5760 on top of base
• Private BUPA healthcare
• Life Assurance
• Pension
• Childcare Vouchers
• 25 days Annual leave which extends to 1 day each year to a max of 27 days.
• Permanent employee of DOCS
• Flexibility of Home working 2 days a week. DOCS provides a Smart Phone and client provides you with laptop

**** Please Contact Tanzina Guerni directly on: 01932 269 754 OR email me your CV at: for more information!***


**Please DO NOT apply if you do not have the right to work in the UK as we cannot provide Sponsorship**

CRO, Pharma, Pharmaceutical, Biotechnology, Biotech, Clinical Research Organisation, Permanent, Clinical Research, Project Management, Senior Project Manager, Manager, ePRO systems, Vendor Management, problem Solving, Presentation, Buckinghamshire, High Wycombe, UAT, User Acceptance Testing, Patient Reported Outcomes, Clinical Trial Manager, Senior Clinical Trial Manager, Clinical Project Manager, Clinical Data Lead, Senior Data Manager, Data Project Leader. 

Apply for this job: Top Global Pharma seeks ePRO Project Manager/ permanent/ Buckinghamshire

Contact Information:

Address:  DOCS UK
2 Globeside, Globeside Business park Marlow
Reasons to work for Docs International
Tel:  +44 (0) 2380 688500
Fax:  +44 (0) 2380 688501
Website:  Visit Our Web Site

Share | | |
Site Map | Privacy & Security | Cookies | Terms and Conditions is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.