Clinical Project Manager at Kansas

Job Description

The Clinical Project Manager will ensure that all allocated projects are carried out in strict accordance with the relevant protocols, analysis plans, SOPs, and the specified standards of GCPs. This position provides relocation assistance to Madison, WI or can be a remote position.

Duties and Responsibilities:

• Clarify specific CDARO (Clinical Data, Analysis and Reporting Organization)  requirements from clients

• Communicate on a regular basis with assigned clients regarding questions, concerns, and project status

• Identifies operational and logistical challenges and solutions

• Organize, chair, and record minutes for all relevant CDARO project meetings

• Facilitate meetings with Sponsors and develop working relationships with client companies

• Ensure the relevant personnel are kept informed of problems that may affect the project performance

• Coordinate receipt and inventory of study related information.  Ensure all appropriate documentation and procedures are performed upon project completion

• Liaise with Quality Assurance regarding regulatory compliance of study reporting and Sponsor audits

• Elicit and coordinate interdepartmental communication

• Document and circulate client interactions

• Communicate with the Data Management, Programming, Statistics, Pharmacokinetics, Medical Writing, and QA departments regarding study progress and reporting requirements

• Update the CDARO timelines for allocated projects in a timely manner.  Renegotiate timelines as appropriate

• Responsible for timely production of deliverables

• Liaise with Covance offices or external data vendors as appropriate with regard to the schedules of data availability

• Liaise with the Sponsor over documentation required for the report preparation process

• Keep CDARO management team and/or client services informed of pertinent project or client related information (i.e., work scope changes)

• Develop an in-depth knowledge of all Covance CDARO capabilities

• Ensure client satisfaction surveys are provided to clients.  Distribute comments to the CDARO study team and managers as appropriate

• Actively promote CDARO services to clients whenever possible

• Write and update SOPs as required

• Performs other related duties as assigned

Job Requirements

Education & Experience Requirements:

• BS or BSc in Science, Medical, or related field

• Knowledge/experience with drug development

• Knowledge/experience clinical research preferred

• 1-2 years of related Project Management experience

• Additional experience may be substituted for education requirements

To Apply Online:  http://jobsearch.covance.com/42020-jobs.aspx

Because of our passion and drive, Covance attracts the kind of people whose contribution has resulted in our exceptional growth. Once a part of our talented team, our employees stay at Covance to work in an environment that encourages career development, allows them to work alongside respected colleagues on challenging projects and provides a diverse global culture.

 

There is no better time to join us!

Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us.

Country: USA, State: Kansas, City: Kansas, Company: Covance.