Recruiting Solutions-posted about 1 year ago
$90,579 - $97,713/Yr
Full-time • Mid Level
Remote • Atlanta, GA
Professional, Scientific, and Technical Services

We are seeking a skilled Project Manager with 5-7 years of experience in the pharmaceutical industry to join our team. The ideal candidate will have a strong background in general project management, with specific expertise in go-to-market activities such as managing Phase 3 clinical trials, coordinating product launches, and organizing marketing events. This role requires excellent organizational and communication skills, as well as the ability to work effectively across multiple teams and functions.

  • Plan, execute, and oversee projects related to the go-to-market process, ensuring timely completion and alignment with business objectives.
  • Organize and manage product launch events and marketing activities, collaborating with marketing and sales teams to maximize impact and reach.
  • Work closely with R&D, regulatory, marketing, and sales teams to facilitate effective communication and collaboration throughout the project lifecycle.
  • Develop and maintain communities of practice within the organization to share knowledge, best practices, and foster continuous improvement in go-to-market processes.
  • Monitor project budgets and resources, ensuring projects are delivered within scope and financial constraints.
  • Identify potential project risks and develop strategies to mitigate them, ensuring project continuity and success.
  • Provide regular updates to stakeholders on project progress, challenges, and achievements, ensuring transparency and alignment.
  • Bachelor's degree is required preferably in Life Sciences, Business, Project Management, or a related field.
  • 5-7 years of project management experience in the pharmaceutical industry, including experience with go-to market activities for product launches.
  • Experience with clinical trials coordination is a plus.
  • Strong organizational and problem-solving skills, with attention to detail and ability to manage multiple priorities.
  • Excellent communication and interpersonal skills, capable of working effectively across diverse teams.
  • Familiarity with regulatory requirements and compliance in the pharmaceutical industry.
  • Ability to foster collaboration and create communities of practice.
  • Experience with clinical trials coordination is a plus.
  • Equal employment opportunities (EEO)
  • Compliance with applicable state and local laws governing nondiscrimination in employment
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