Clinical Research Project Coordinator, Division of Nephrology at SickKids
Toronto, ON M5G 1X8, Canada -
Full Time


Start Date

Immediate

Expiry Date

14 Dec, 25

Salary

0.0

Posted On

16 Sep, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Clinical Research Experience, Adobe Creative Suite, Stata, Ease, Redcap, Computer Skills, R

Industry

Pharmaceuticals

Description

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.

ESSENTIAL REQUIREMENTS:

  • A Master of Science which includes clinical research experience or at least 3 years of relevant (as per activities above) clinical research experience.
  • Strong computer skills that include database management (Microsoft Office Suite is a must; Familiarity with RedCap, and Adobe Creative Suite is an asset).
  • Ability to conduct literature searches and maintain literature databases.
  • Excellent communication (oral and written), organization and problem-solving skills.
  • Ability to function independently (highly important), yet collaboratively within a multi-disciplinary team.
  • Ability to manage multiple competing demands and deadlines with ease.
  • Self-motivated and detailed oriented.
  • A commitment to understanding and aiding in the pursuit of equity, diversity and inclusion objectives.

PREFERRED QUALIFICATIONS:

  • Clinical professional degree or certification as a clinical research associate (e.g., SOCRA, ACRP accreditation) or Project Management Professional (PMP).
  • Experience with grant submissions, reviewing legal contracts and helping to facilitate contract execution.
  • Familiarity with statistical software packages (e.g., SPSS, STATA, or R)
    Employment Type: Full-time temporary 1 year contract with modified benefits (i.e., health & dental).

How To Apply:

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Responsibilities

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