SEC Recruitment

Lead Data Manager - Real World Evidence - Home based

Location
England
Salary
40,000 - 60,000
Posted
23 Oct 2018
Closes
31 Dec 2018
Ref
BBBH113992
Contract Type
Permanent
Lead Data Manager - Real World Evidence - Home based (anywhere in Europe) – €50,000 to €55,000 per year – CRO – Permanent role

If you would like to apply for the position please call Mark on 0044 (0) 207 255 6665 or email your CV with a brief covering note to mark.wilkins@secpharma.com

Real World Evidence trials are becoming ever more important as the shift towards metadata analysis becomes more and more important. If you haven’t worked on Late stage/Real world evidence trials then this may be the opportunity to do so. We are working closely with a leading service provider to the Pharmaceutical industry in the search for a Lead Data Manager. In this role you will be the single point of customer contact for all studies you are involved with and have complete project oversight from the Clinical Data Management perspective. You will be tasked with complete and timely delivery of all study requirements with a focus on data quality. You will be working on Late Phase studies only

Not only is this company renowned for training and developing their staff, they are a company provide leading edge capabilities to their clients around the globe. The company will invest in your development and give you the tools to progress your career and work with the best technology in the industry.

Your key duties and responsibilities of our current opportunity include -

Client Management:

- Serve as primary point of contact for customer on data management deliverables and provide project management expertise working with customer DMs, key decision makers and internal team members to manage continuous process improvements, issue escalation, workload projections, and provide technical expertise
- Maintain strong customer relationships

Service Management:

- Meet with cross functional team members on a regular basis to ensure milestones meet timelines and quality deliverables
- Establish strong communications with Data Operations team, functional leads, project managers and all other stake holders
- Serve as the escalation point for unresolved data issues; work with client data managers, vendors, internal team members for resolute
- Create and/or review and sign-off on all data management plan (DMP) documents
- Ensure timely follow-up and resolution of compliance and Serve as Subject Matter Expert

Financial Management/Business Development Support:

- Ensure service and quality meet agreed upon timelines and deliverables in contract/Scope of Work (SOW)
- Manage SOW/budget
- Review financial reports on a monthly basis and participate in project reviews as requested

Other:
- Independently bring solutions to the CDM team/CDM department
- Lead and/or participate in a focus team or global or local best practice team
- Present at professional conferences and/or publish articles in professional journals

MINIMUM EXPERIENCE REQUIRED

- Thorough knowledge of the data management process and experience in specialized data management skills – Ideally in a Real world evidence trials but in fact lead DM experience in Phase II or III will be enough.
- Study Lead experience of more than 3 years. You must have been the key point of contact for your trials and led the meetings.
- Experience including proven competence in managing delivery of multiple projects simultaneously through full data management study life-cycle, including large trials of over 1000 patients, including experience handling customer negotiations (e.g. bid defence meetings)

A full job description is available on request

If you would like to apply for the position please call Mark on 0044 (0) 207 255 6665 or email your CV with a brief covering note to mark.wilkins@secpharma.com