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Study Manager

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About the role

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"At ICON, it's our People that set us Apart"
 
 
Do you have experience assessing and apply project management knowledge to ensure that the project is completed in accordance with the scope, quality, timelines and cost of the contract?
 
Study Manager Role within ICON: 
 
ICON has a strong reputation in our approaches to clinical development.   We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients.   We work with top pharmaceutical organizations on emerging therapeutic areas which include but are not limited to Oncology, Vaccines, CNS, Cardiovascular and Pain.  We are presently in over 40 countries with over 80 offices worldwide and over 10K employees globally. 
 
The study manager will work with cross-functional sections/teams to deliver clinical study projects under the constraints of study scheduling and resources.  You will ensure adequate staffing and training of staff working on assigned projects and act as the primary liaison between the project team and the client.
 
  • Ensure that all outside vendor contracts are set up and deliverables are being meet in accordance to the agreed upon work order.
  • Obtain and review clinical statement of work (SOW) and/or study work order (SWO) to determine what services are required for each clinical trial protocol.
  • Initiate and participate in the early planning phases of clinical study by providing guidance on deliverables and outsource options (i.e. assist in preparation of study proposal timelines, scheduling and other study requirements as appropriate); including but not limited to study source documents, procedural timelines and lab set up.
  • Work closely with clinical research coordinator to ensure adequate internal resources and resolution of any clinical study work flow issues for assigned clinical studies.
  • Prepare and maintain project management plan for assigned clinical studies.
  • Act as liaison and point of contact for all clinical study sponsors and vendors for related services.
  • Attend sponsor meetings and required conference calls to ensure effective communication flow between external customers and staff.
  • Present at Clinical Tracking Meetings
 
Benefits of working at ICON:
In addition to partnering with the top pharmaceutical and biotech companies in the world we offer a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, bonus plans, vacation, and other incentives.  
 
To succeed you will need:
We are seeking candidates with a Bachelors’ degree in a related field strongly preferred with a minimum of two years clinical research experience leading and directing clinical trials as a clinical research coordinator. In lieu of a bachelor’s degree a high school diploma and a minimum of 5 years clinical research experience leading and directing clinical research in required.
 
To be successful you will be expected to have excellent written, oral and interpersonal skills. You must have strong problem-solving skills and be detail-oriented with excellent organizational and prioritization skills.  Ability to work on multiple projects simultaneously and meet varied deadlines .Ability to understand protocol requirements to apply project management knowledge to: initiate, plan, execute, monitor/control and close clinical study. Proficient with Microsoft Office.
 
 
We invite you to review our opportunities at www.iconplc.com/careers.
 
What’s Next?
 
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.
 

ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment

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