Clinical Studies Support Coordinator

By Select Source International Posted On 03/14/2017 Plymouth, Hennepin County, Minnesota, United States
1 - 4Years Job Type:  Contract Joining Time: Immediate
Hourly Rate: USD 30 - 40 / Hour(Negotiable)
  • Education:  N/A
  • Functional Area:  Research
  • Industry:  Medical/Healthcare/Hospital
KEY SKILLS:  clinical researchgcpstudycoordinatorsupportfda

Job Description

Job Title                :          Clinical Studies Support Coordinator

Location               :          Plymouth, MN

Duration              :          24+ Months Contract

 

Description:                                            

Provide support to the Peripheral Clinical Program. The Coordinator will independently perform diverse administrative and project duties.

 

Position responsibilities:

• Provide project support for clinical study teams and/or department

• Maintain study-specific correspondence and other required documentation

• Assist in the coordination of meetings and meeting logistics

• Assist in the organization and distribution of clinical study documentation

• Assist in tracking study activity, such as start-up progress by ensuring receipt of proper study documentation, agreements, and site approvals

• Work with clinical team to create and distribute newsletters and communications to sites

• Attend team meetings, taking notes on discussion points and action items

• Support daily projects where the use of Excel, Power Point, SCTMS, and RAD is required

• Solve problems of moderate scope and complexity following established policies and procedures

• Identifies issues in documents, memos, correspondence, and telephone calls which require action. Recommends alternatives and executes alternative when appropriate.

• Drafts brief project related documentation

• Perform various study duties including facilities coordination, project document organization and reconciliation, setting up files, ordering supplies/equipment, photocopying

• Works under general supervision

• Other duties as assigned

 

Minimum Education Required: High School degree or GED

 

YEARS OF EXPERIENCE: 6+ years' experience in clinical study administration

OR 4+ years' experience in clinical study administration with Associates degree (3+ years with Bachelor's degree)

 

Specialized Knowledge Required: Experience with word processing, spreadsheets, and database applications (e.g. MS Word and Excel)

 

Desired/preferred qualifications:

• Bachelor degree in health science or business related field

• Working knowledge of medical terminology

• Proficiency in GCPs, regulatory and compliance guidelines for clinical trials

• Advanced oral and written communication skills

• Attention to detail and accuracy

• Ability to manage and prioritize multiple tasks

• Effectively work independently and in a team setting

About Company

Select Source International is a Global Solutions provider of IT staffing and Project services. Our service offering has 5 main practices; ERP, Application Development, Middleware, Database Management and Project Services. SSI offers industry leading Data Migration, Compliance, and Risk Management through its subsidiary Data Wave. Data Wave offers Cyber Security and risk management through a GRC product suite called Risk Utilities. In addition to our technology offerings, SSI also provides administrative and business consulting services. Industry Experience: Retail Healthcare Manufacturing Energy and Utilities Government Financial Engineering.

Recruiter Details

  • Name: Mukesh Sharma
  • Email: mukeshs@selectsourceintl.com
  • Phone: 9525463300
  • Extension: 6003

Company Detail

 

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