Local Trial Manager (LTM) - Canada at Amgen
Vancouver, BC V6G 1C9, Canada -
Full Time


Start Date

Immediate

Expiry Date

19 Sep, 25

Salary

124000.0

Posted On

20 Jun, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Global Teams, Trial Management, Life Sciences, Clinical Research Experience, Clinical Trials, Oversight

Industry

Pharmaceuticals

Description

HOW MIGHT YOU DEFY IMAGINATION?

You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.
Local Trial Manager (LTM)

BASIC QUALIFICATIONS:

Master’s degree & 3 years of directly related experience
OR
Bachelor’s degree & 5 years of directly related experience
Advanced knowledge of global clinical trial management

PREFERRED QUALIFICATIONS:

  • BA/BS/BSc
  • Minimum 2-3 years’ experience of leading local/regional or global teams
  • Minimum 2-3 years’ clinical trial project management experience
  • 7 years’ work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
  • Experience in management and oversight of external vendors (e.g., CROs, central labs, imaging vendors, etc.)
  • Must be a local/country expert with identifiable project management experience locally
  • Build strong site relationships as well as other local relationships to ensure end to end study delivery is met.
Responsibilities

Let’s do this. Let’s change the world. In this vital role you will be the primary point of contact to lead, manage and co-ordinate the conduct of clinical trials from study start-up to close out (CSR/Archival) at a country level in accordance with ICH-GCP and other applicable local regulations. You will maintain the quality and scientific integrity of clinical trials at a local/country level and actively collaborate with cross functional internal and external partners to ensure timely delivery, budget implementation of clinical trial results within the local country.

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