Project Manager - III

Intelliswift Software
Foster, CA Full Time
POSTED ON 8/30/2024 CLOSED ON 9/25/2024

What are the responsibilities and job description for the Project Manager - III position at Intelliswift Software?

We are seeking a highly organized and detail-oriented Research Project Manager to oversee and manage nonclinical research projects. The ideal candidate will have a strong background in project management within the pharmaceutical or biotech industry, excellent communication skills, and the ability to work collaboratively with cross-functional teams.

Key Responsibilities

  • Maintain and track nonclinical project plans.
  • Coordinate and facilitate communication nonclinical subteams and development teams.
  • Oversee project updates, presentations reports, senior management and stakeholders.
  • Ensure compliance with regulatory requirements and company policies.
  • Foster a collaborative and innovative team environment.
  • Conducts effective meetings with clear objectives and seeks to gain cross-functional input, assess risks, and solicit alternative views for decision making; develop agendas, take meeting minutes, follow up on action items.

Qualifications

  • Minimum of B.S. in a relevant scientific discipline (e.g., biology, chemistry, pharmacology).
  • 3 to 5 years of project management experience in the pharmaceutical or biotechnology industry, with a focus on drug discovery is preferred.
  • Minimum of 3 years of experience in the pharmaceutical or biotechnology industry, with a focus on drug discovery.
  • Strong understanding of the drug discovery process and nonclinical support, from IND to Ph 3, including life-cycle support.
  • Excellent organizational, communication, and leadership skills.
  • Proven ability to manage multiple projects simultaneously and meet deadlines.
  • Proficiency in project management software and tools.
  • Ability to work effectively in a fast-paced, dynamic environment.

Preferred Qualifications

  • PMP (Project Management Professional) certification.
  • Experience with regulatory submissions and compliance.
  • Basic knowledge of Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) guidelines.

Benefits

  • Collaborative and inclusive work environment.
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