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Required! Clinical Trials Project Co – ordinator – Courtesy (Pharma job.ca)
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SickKids

Job Description
Job Title:
Clinical Trials Project Coordinator
Job ID:
4065
Location:
Toronto, Ontario
FTE:
1.00
Hours of Work:
35.00
Dept/Program Name:
Clinical Trials Support Unit
Contract Length:
1 year
2015-05-20
Date Posted:
2015-05-28
About SickKids

Dedicated exclusively to children and their families, The Hospital for Sick Children (SickKids) is one of the largest and most respected paediatric healthcare centres in the world.  As innovators in child health, we lead and partner to improve the health of children through the integration of healthcare, leading-edge research and education.  Our reputation would not have been built – nor could it be maintained – without the skills, knowledge and experience of the extraordinary people who come to work here every day.  SickKids is committed to ongoing learning and development, and features a caring and supportive work environment that combines exceptionally high standards of practice.

When you join SickKids, you become part of our community. We share a commitment and determination to fulfill our vision of Healthier Children. A Better World.

Don’t miss out on the opportunity to work alongside the world’s best in paediatric healthcare.

Position Description

Are you interested in a career with the research team conducting pediatric clinical trials?  We are currently looking for a Clinical Trials Project Coordinator (CRA2) to join our dynamic team in Hematology/Oncology at the Hospital for Sick Children.

As a Clinical Trials Project Coordinator you will focus on Neuro-Oncology and Solid Tumours.  In this role you will work collaboratively with the oncology team of physicians, nurses, project managers and other project coordinators.  You will be responsible for initiating, planning and coordinating clinical trials studies from start up to close out.  You will also be responsible for an international registry start up. This is an exciting opportunity for you to use your clinical trial project coordinator and project management skills in a pediatric oncology setting.

Here’s What You’ll Get To Do

  • Regulatory submissions for scientific and ethical review throughout lifecycle of the study
  • Study feasibility review; budget preparation
  • Patient enrollment; eligibility review
  • Data abstraction and submission; specimen submission
  • Monitor study compliance, collaborate with medical staff to assure completeness and accuracy of documentation, facilitate use of the protocol as well as maintain quality assurance through accurate and timely data reporting
  • Liaise with CTPMs, nursing, physicians, other members of the health care teams and other CTPCs, study coordinators and regulatory personnel
  • Participate in educational initiatives concerning clinical trials and attend related meetings

Here’s What You’ll Need

  • Baccalaureate degree in a related discipline
  • Certification as a Clinical Research Professional or willingness to write the examination
  • Minimum of 3 years experience in clinical trials, including regulatory and clinical data management
  • Prior experience in oncology is required; experience in paediatric oncology is a strong asset
  • Knowledge of medical terminology
  • High energy individual with excellent organizational and analytic skills
  • Demonstrated exceptional interpersonal and communication skills
  • Demonstrated ability to utilize critical thinking and problem solving abilities
  • Strong computer skills
  • Self motivated and able to work independently as well as within a team

Employment Type

Temporary Fixed-term, 1 year maternity leave coverage, 35 hours per week

SickKids Job Title: CRA 2

Our Commitment to Diversity

SickKids is strongly committed to diversity within its community and welcomes applications from visible minority group members, women, Aboriginal persons, persons with disabilities, members of sexual minority groups and others who may contribute to diversity within our organization.

SickKids is also committed to providing services in both official languages and our preference is to hire employees who are fluent in both English and French whenever possible.

Thank you for your interest in joining SickKids. Only those applicants selected for an interview will be contacted. In accordance with our Hospital policy, employment at SickKids is conditional upon the Hospital’s receipt of all necessary documentation.

How to Apply

Tip: Combine your cover letter and resume into ONE document as youcannot upload multiple documents as part of your application.

Tip: Ensure that the name of the document containing your covering letter & resume does not contain special characters, symbols or accent symbols (é, : / ? * [ ]) as this will prevent you from being able to successfully upload your document.

Tip: When uploading you resume avoid using the Cut/Paste Cover Letter/Resume option as resumes are not formatted and difficult to read.

Tip: After uploading your resume look for any items that indicate ‘Please update’ or are blank in theWork Experience or Degree section.  If you notice any blank sections select the link and either update the information or use the garbage icon to remove this item from your application. You will not be able to submit your application until all missing items have been either updated or deleted.

Technical Assistance

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If you are still experiencing technical difficulties please email ask.hr@sickkids.ca to send us a short description of the issues you are experiencing. Please note that we will not accept resumes sent to this inbox but we are happy to respond to requests for technical assistance.

Copy and paste the link below to apply

http://www.pharmaceutical.ca/en/job-offers/on/toronto/hospital-for-sick-children-the-6829/clinical-trials-project-coordinator/701450



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