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Job Details

Project Data Manager - Homebased anywhere in EU

Company: Chiltern
Location:
Reference: PDM - EU
Closing Date: 10 Aug 18
Type: Full Time
Salary (£): On Application
Benefits:

Job Summary:

We are currently looking to recruit experienced Project Data Managers for our Biometrics group. Candidates with significant prior experience and a proven track record in delivering on projects will be considered for the Project Data Manager role.  

Requirements:

Chiltern: A global contract research organization. We are the leading mid-sized provider of clinical solutions in a variety of specialty areas and engagement models for biopharmaceutical and medical device industries. We operate out of 47 different countries, have managed over 1800 studies and have just over 4300 staff.

 

We are currently looking to recruit experienced Project Data Managers for our Biometrics group. Candidates with significant prior experience and a proven track record in delivering on projects will be considered for the Project Data Manager role.  

 

We are looking for like-minded people that want a job designed for career success. Experience in any of the following Data Systems would be beneficial.

 

• Medidata Rave®

 • MedNet, iMedNet™

• Merge eClinicalOS®

 • Oracle® InForm

• Perceptive DataLabs®

 

We can offer competitive salaries, benefits that are designed around you and a strong support mechanism and dedicated coaching to develop your career within Data Management.

 

This is a full time permanent opportunity. Home based.

 

Primary duties:

 

  1. Collaborate with respective project sponsor and stakeholders to develop effective project plans to include scope, goals, deliverables, required resources, risks, issues and milestone timing.

 

  1. Effectively plan and execute multiple Data Management projects simultaneously. Provide updates directly to senior stakeholders as requested by line management
  2. Participate in Business Development presentations and bid development

 

  1. Support the production of bids and proposals development

 

  1. Assign tasks and responsibilities within Data Management to team members, in a manner that: optimizes team capability; delivers timely and accurate results; and supports the needs of the business

 

  1. Ensure that assigned team executes Data Management functions in accordance with Chiltern and/or sponsor Standard Operating Procedures (SOPs)

 

  1. Provide guidance to less-experienced Project Data Managers

 

  1. Assess ongoing and future project resource needs on an ongoing basis with feedback to Line Management

 

  1. Clearly communicate expectations to team members and stakeholders.

 

  1. Resolve any issues and solve problems throughout project lifecycle.

 

  1. Manage sponsor relationships and triage issues as appropriate

 

  1. Ensure that project team member performance supports project budget and delivery requirements

 

  1. Effectively manage project scope by ensuring any changes to scope are documented and approved through appropriate change management processes.

 

  1. Effectively lead a team of cross-functional associates towards common project goals. Proactively identify and address team cohesion obstacles to project success.

 

  1. Participate in and/or contribute to Sponsor and/or Regulatory audits/inspections

 

  1. Participate/attend Sponsor requested meetings as required. Perform other duties as required by the Department. 

 

Requirements:

 

• Life Sciences degree

• Ability to maintain confidentiality of data and information during interactions with staff at all levels

• Prior experience in Data Management in the pharmaceutical, biotechnology, medical device/diagnostics or clinical trial industries.

• Effective communication skills

• Working experience with Medidata Rave, Inform and Oracle Clinical is preferred

• Strong leadership qualities and experience of supervising other Data Managers

• Hands on experience with EDC systems

• Good knowledge of the drug development life cycle

• Understanding of the principles of ICH GCP and regulatory requirements

• Good computer literacy with working knowledge of Windows and Microsoft Office applications

• Good oral and written communication, organisational skills and personal presentation

• The ability to communicate effectively in English

• Experience working within a team environment under time and resource pressures

• Proven experience in clinical trials with knowledge of SOPs, regulatory reporting requirements and accepted practices

• Confident dealing with external and internal clients and providers

Apply for this job: Project Data Manager - Homebased anywhere in EU

Contact Information:

Address:  France
37 bis rue de Villiers, 92200 Neuilly sur Seine, France

France
Tel:  +33 1 41 05 73 00
Fax:  +33 1 41 05 73 01
Website:  Visit Our Web Site

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