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Clinical Research Manager (Devices)

Toronto - Ontario - Canada - Life Sciences & Health Care - Medical devices - Research & Development - Other

Our client is seeking a dedicated Clinical Device Research Manager to join their reputable medical device company. C

They are offering a competitive compensation package, a collaborative work environment and an excellent work/life balance. Apply now if you are interested in this exciting and challenging full-time position.

Feel free to contact

Diana Grodowski, Account manager

Apply now

About this role

RESPONSIBILITIES:

  • Prepare clinical development plans for new devices or modifications to existing devices;
  • Identify timelines, resource requirements and budgets for multiple clinical studies;
  • Outline proper study design & documentation including but not limited to Protocol, CRF, ICF, SIV as well as Source and Regulatory documentation as required;
  • Manage process from Study execution through completion, data analysis, summary and creation of scientific papers or abstracts;
  • Ability to Identify/Recommend investigators as well as initiate clinical studies and provide staff training;
  • Monitor clinical investigations, assuring protocol compliance, subject welfare and data integrity;
  • Ensure compliance with Corporate SOPs and Regulatory Authorities;
  • Maintain Clinical File structure according to standard GCP policies and regulatory guidance;
  • Maintain strong professional relationships with Key Opinion Leaders and Clinical Research sites.

About you

Our client is seeking a Clinical Research Manager with the following Education and experience:

QUALIFICATIONS:

  • BS, RN or Master’s degree in medical life sciences;
  • Five or more years as Clinical Research Associate or equivalent;
  • Minimum 2-3 years in Clinical Research Supervisory role;
  • Strong interpersonal skills in the management and development of employees;
  • Excellent analytical, organizational, and problem-solving skills;
  • Ability to function as an independent investigator and able to multitask and prioritize tasks;
  • Experience with energy-based devices;
  • GCP or Clinical Trial Design certification (medical device a plus);
  • Complete understanding of Regulatory / GCP guidelines associated with research programs;
  • Must have a valid driver’s license and a valid passport;
  • Excellent writing, presentation and communication skills;
  • Fluent in English, both written and verbal;
  • Flexibility for occasional evening or weekend work, worldwide travel as needed -25-50 % (worldwide travel).

What we offer

Brunel Life Sciences provides global staffing, recruitment, and contracting solutions for Life Sciences, Pharmaceutical, Biotechnology and Healthcare organizations. Brunel Life Sciences plays a vital part of the Brunel International Group, with over 100 offices in 40 countries and approximately 13,000 employees around the globe.

About us

Our client is an innovative Medical device company, with emphasis in dermatology. They are creators of breakthrough technology designed for health and wellness.

Summary

  • Vacancy number: PUB162445
  • Location: Toronto
  • Market: Life Sciences & Health Care
  • hours per week: 40
  • Branche: Medical devices
  • Education level: Other
  • Area of Expertise: Research & Development
  • Closing date: Sunday, June 24, 2018
Apply now

Feel free to contact

DG

Diana Grodowski

Account manager Brunel Canada Toronto

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