Project Manager, Early phase / Gestionnaire de projet, phase précoce
at Innovaderm Research
Remote, British Columbia, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 23 Jan, 2025 | Not Specified | 24 Oct, 2024 | N/A | Regulations,French,Clinical Trials,Clinical Research,English,Clinical Monitoring,Vendor Management,Timelines,Clinical Practices | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
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OPT | H4 Spouse of H1B |
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Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Projects Managers are crucial to the success of Clinical Trials managed by Innovaderm. They are the main point of contact internally as well as externally, ensuring all activities and deliverables are completed on time, on budget, and as expected.
Great project managers go further than creating project plans and following up on tasks. They show leadership to help project teams focus on objectives and deliver results.
EDUCATION
- B.Sc. in a related field of study to clinical research
- M.Sc. or Ph.D. an asset
EXPERIENCE
- At least 5 years of industry experience, including a minimum of 3 years in Phase I-II clinical trial project management
- Experience leading concurrent multi-centered clinical trials involving multiple countries / regions is an asset
- Experience in one or more of the following considered an asset: study start up, regulatory submission, clinical monitoring (CRA), or vendor management
- Experience managing dermatology trials an asset
KNOWLEDGE AND SKILLS
- Excellent knowledge of GCP and ICH standards, FDA and local country regulations
- Excellent knowledge of Microsoft Office suite
- Fluency in English with excellent oral and written skills, required
- Bilingualism (English and French) is an asset
- Ability to work in a team environment and establish good relationships with colleagues and sponsors
- Strong ability to carry out different projects and work under pressure while meeting timelines
- Good knowledge of good clinical practices, and applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines
- Good problem-solving, critical- and creative-thinking abilities
- Strong scientific acumen
- Strong cross-functional knowledge in clinical research
Our company:
Responsibilities:
THIS ROLE WILL BE PERFECT FOR YOU IF:
- You are a hands-on project manager who enjoys working on multi-site early phase projects including Phase I, Phase IIA / proof of concept as well as Investigator-Initiated studies.
- You enjoy helping look for ways to improve and simplify processes to better respond to the needs of Early phase projects in a regulated environment.
- You wish to work for a mid-sized CRO that works on significant multisite trials
- You are looking to position yourself in an environment where you can grow your career alongside of a growing company.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
IT Software - Other
Clinical Pharmacy
BSc
Proficient
1
Remote, Canada