Associate Project Manager, CMC, Remote Canada

Associate Project Manager, CMC, Remote Canada
POINT Biopharma, Canada

Experience
1 Year
Salary
0 - 0
Job Type
Job Shift
Job Category
Traveling
No
Career Level
Telecommute
Qualification
Bachelor's Degree
Total Vacancies
1 Job
Posted on
Aug 4, 2022
Last Date
Sep 4, 2022
Location(s)

Job Description

POINT Biopharma is an innovative, high-performance company focused on a hard problem: creating new cancer therapies that are more effective and have fewer side effects than traditional treatments. Our products are targeted radioligands, a technology that hold significant promise to treat cancer. Our company is growing rapidly: we just announced a phase 3 clinical trial for our novel radioligand based prostate cancer treatment, established our U.S. manufacturing center in Indianapolis, and have a pipeline of next generation oncology products in development. We are a creative and agile team accountable to a high standard: to be uniquely better. If you are searching for new and uniquely better career path, you should consider joining the POINT team.

TO BE CONSIDERED, APPLICANTS MUST BE LEGALLY ENTITLED TO WORK IN CANADA.

Location of work - work remotely, preferably the Greater Toronto Area

The position will be working remotely with the anticipation of travel for team and client meetings. Currently, our employees are working remotely and located within the Eastern Time Zone. To work in synergy, it is preferred that our applicants are working within the same Eastern Time Zone to accommodate team and client meetings.


Overview

Reporting into Senior Manager, Process Chemistry, the Associate Project Manager, Chemistry Manufacturing amp; Controls will assist with the planning and management of external vendor activities for the execution of clinical and commercial projects whilst adhering to budget, scope and schedule requirements for POINT Biopharma. This position would also require liaison with internal project teams from various departments, such as Clinical Supply Chain, Regulatory Affairs, Clinical Development, Manufacturing, Preclinical, and Quality Assurance.


Responsibilities

Lead project management efforts through successful planning with diverse teams:

  • Prepare and maintain project plans, obtaining management approval and project team buy-in; liaising with external vendors as appropriate.
  • Facilitate supply chain and logistics both internally and with external vendors; routinely monitor status and communicate as required.
  • Analyze actual performance against the plan and make adjustments consistent with plan objectives. Facilitate cross-functional project team meetings with internal and external stakeholders.
  • Develop, track, and monitor project goals in accordance with CMC strategy; ensure project goals are cascaded as actionable tasks and subsequently executed upon.
  • Make best use of modern communication techniques as you excel at working in a virtual remote global setting.
  • Maintain project documentation to promote engaging project team environment, including document management (Sharepoint), taking minutes, updating project timelines, etc.
  • Able to comprehend business processes in application to external vendor relationships, including management of purchase orders, invoices etc. in collaboration with Finance.


Analyze projects’ performance:

  • Direct liaison with external stakeholders (e.g., CMO, vendors, and collaborators) for related projects in CMC.
  • Maintain and develop tools and processes to assist in project tracking and execution.
  • Assist in the technical writing and delivery of data analyses, reports, summaries, and presentations; provide status updates for ongoing projects.
  • Communicate proactively with stakeholders and management regarding project risks, delays, and high-impact tasks, along with proposed mitigation plans.
  • Establish and publish clear priorities among project activities.
  • Manage multiple concurrent projects with aggressive and challenging timelines; successfully prioritize workload in accordance with business goals.


Identify improvement opportunities:

  • Possess project management expertise to effectively partner with stakeholders to ensure project management plans (and their various components) are created and maintained with aim to be catalytic in achieving the project goals.
  • Consult and contribute to POINT’s Project Management knowledge and processes.

Requirements

  • BS in a related field
  • CAPM or working towards certification is considered an asset
  • Certification or expertise in Lean, Six Sigma, or Agile is considered an asset
  • Functional knowledge of GMPs and applicable Health Canada, FDA, EMA, ICH, PDA amp; ISPE Guidelines
  • 3+ years of relevant working experience in the pharmaceutical/biotechnology industry in clinical phase operations, radiopharmaceutical preferred
  • 1+ years of project management experience
  • Experience with JIRA, MS Project, and/or similar project management tool(s)
  • Organized and systematic approach to prioritization
  • Abilit

Job Specification

Job Rewards and Benefits

POINT Biopharma

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