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Job Details

Senior Clinical Project Manager - Biopharma

Company: Chiltern
Location: Home or Office based in the US or Canada
Reference: 7089
Closing Date: 22 Mar 18
Type: Full Time
Salary (£): On Application
Benefits: Excellent and competitive benefits

Job Summary:

Home or Office based Senior Clinical Project Manager. Experience in the following TA's preferred: Dermatology, GI, Rare Diseases, or Ophthalmology. Other TA experience will be considered.


Job Background


Senior Project Manager  

(home or office based position)

The Senior Project Manager is responsible for the day-to-day cross-functional operations of the assigned study or studies for one or more clients. As the team leader, the Senior Project Manager will ensure assigned studies are delivered successfully, on-time, within budget, according to client expectations and with the highest level of quality possible. In this role, the main overall responsibilities of the position are the following:

  • Oversee one or more national, international or global studies
  • Oversee the project from receipt of RFP until completion. Activities include (but are not necessarily limited to) managing a multidisciplinary team for designated projects to ensure quality and integrity of data, compliance with either Chiltern or Sponsor’s SOPs, ICH GCP, relevant SOPs and regulatory requirements.
  • Develop project schedules of tasks with input from project team members.
  • Identify and communicate the resources necessary for successful completion of the project.
  • Ensure that the client and senior management are informed in writing of the status of the project, and that any risks to successful completion are promptly addressed.
  • Ensure that assigned projects meet delivery and budgetary targets, using tools as defined in the PM Connect Methodology.
  • Conduct all activities according to the defined project-specific quality and performance standards as well as relevant SOPs, ICH/GCP, and local requirements.
  • Perform other duties as required by the Department.

Desired Skills and Experience

  • We require a 4 year or equivalent college degree from an appropriately accredited institution, preferably in science or nursing or applicable institution, or applicable industry-related experience
  • Minimum of 5 years of clinical trial experience in pharmaceutical, device, biotech or CRO setting.
  • Previous experience managing large multi-center studies, including international studies
  • Must have cross-functional project management experience from the CRO perspective


depends upon experience

Position Type

Full Time


Email Michelle Gerardi -
+1 774 272 5506

Apply for this job: Senior Clinical Project Manager - Biopharma

Contact Information:

Address:  Illinois, USA
1425 Tri-State Parkway, Suite 110 Gurnee, USA
IL 60031
Website:  Visit Our Web Site

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