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Job Details

Lead Clinical Data Manager (UK)

Company: Covance
Location: Maidenhead office or field based within the UK
Reference: 61542BR
Closing Date: 10 Dec 16
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

We are recruiting for our Clinical Data Management team in Europe and are currently seeking to hire a Lead Clinical Data Manager to take the lead on assigned projects and ensure the quality of work across the team. This role is based in our Maidenhead office or field based within the UK. This is a permanent role with excellent career progression.

Requirements:

COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. 

We are recruiting for our Clinical Data Management team in Europe and are currently seeking to hire a Lead Clinical Data Manager to take the lead on assigned projects and ensure the quality of work across the team. This role is based in our Maidenhead office or field based within the UK. This is a permanent role with excellent career progression.


About the Job

Within this role, you will serve as the technical leader on all data management aspects for project(s) including start-up, maintenance, and completion activities. This will include: 

  • Develop [Global] Data Management Plans and Quality Management (QM) Plans that will deliver accurate, timely, consistent, and quality clinical data 
  • Identify and implement solutions to project data management issues and concerns, including proactive prevention strategies based on metrics and forecasts 
  • Serve as the project and client liaison including management and provision of project specific data management status, cycle time, and productivity metrics 
  • Coordinate and participate in the development of the clinical data model and/or database design and annotate the CRF (eCRF) according to these specifications 
  • Review data acquisition conventions and data review guidelines / diagnostic specifications consistent with the clinical data model, [statistical] analysis plans, and CRF (eCRF) completion / monitoring conventions 
  • Coordinate the development and testing of data management system edit / data validation checks (diagnostics) and special listings / procedures used as tools for the data review and discrepancy management activities 
  • Interact and collaborate with other project and specialty team members (clinical, programming, statistics, CDM technical support, drug safety, etc.) to support the set-up, maintenance, and closure of the data management aspects of the project to ensure consistent, cohesive data handling and quality 
  • Advanced planning and risk management for projects (issue escalation, resource management) 
  • Oversee the technical performance of the data review project staff on achieving client satisfaction through delivery of quality data, on-time and on-budget 
  • Assist with goal creation and performance review assessment for data review project staff 
  • Maintain technical data management competencies via participation in internal and external training seminars 
  • Ensure project staff are trained and adhere to project-specific, global, standardized data management processes 
  • Identify areas for process and efficiency improvement and implement solutions on assigned projects 
  • Support achievement of project revenue and operating margin for data management activities to agreed targets 
  • Develop and maintain strategic client relationships and receive client satisfaction surveys and implement appropriate action plans as necessary 
  • Support business development for data management time and cost estimates and prepare and present to potential clients on global data management capabilities. 
  • Review literature and research technologies/procedures 


About You:

To be successful in this position, you will need to hold a University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology). 

  • A high degree of demonstrable relevant work experience in data management including working knowledge of the technical supervision / matrix management of team members to include data management, clinical operations, and knowledge of several therapeutic areas. 
  • Demonstrated skill for technical management of staff exceeding 5 employees. 
  • Financial management of gross revenues in excess of $250K per year 
  • Excellent oral and written communication and presentation skills. 
  • In depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations 
  • Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies. 
  • Ability to lead by example teams on project strategies and achievement of department goals, objectives, and initiatives and to encourage team members to seek solutions 
  • Demonstrated managerial and interpersonal skills. 


We Offer:

COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. 

Covance’s ongoing success offers team members unsurpassed growth and career development opportunities. 

At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. This is your chance to become part of a team that helps to bring miracle of medicine to market sooner. 

There is no better time to join us!

 

keywords:

Clinical research, clinical data management, data management, CDM, CDARO, data management plan, ADaM, CRO, Clinical Data Management, database lock, Clinical Data Manager, Data Manager, CDM, Medidata, Rave, inForm.

Apply for this job: Lead Clinical Data Manager (UK)

Contact Information:

Address:  Covance- Maidenhead


England
Tel: 
Fax: 
Website:  Visit Our Web Site

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