Full Time

Senior Clinical Program Manager (Contractor) (Office OR Remote)

Arcus Biosciences
Remote!
$95,000 - $120,000* / year (about $46–$58 an hour)

Job Description

This job was posted over 30 days ago, so it has most likely closed. See newer jobs like it.

Written by AI from the job title and company, not by Arcus Biosciences, so some details may not match this job. The employer's own page has the real description.

Job Overview

The Senior Clinical Program Manager (Contractor) at Arcus Biosciences plays a critical role in overseeing and managing clinical trial programs. This position involves leading cross-functional teams to ensure that clinical trials are executed efficiently and effectively. The successful candidate will be responsible for developing program strategies, coordinating resources, and ensuring compliance with all regulatory requirements, while fostering communication amongst stakeholders. The role demands a strong emphasis on project management, strategic planning, and team leadership, contributing to the advancement of innovative therapeutic solutions.



Job Responsibilities

  • Lead the planning, implementation, and execution of clinical programs in collaboration with cross-functional teams.
  • Develop and manage project timelines, budgets, and resources to ensure efficient trial conduct.
  • Ensure compliance with regulatory requirements, industry standards, and organizational policies.
  • Act as the primary liaison between internal stakeholders and external partners, such as CROs and clinical sites.
  • Monitor trial progress and proactively identify and mitigate risks to keep projects on track.
  • Prepare and present project updates to senior management and other stakeholders.
  • Support the development of study protocols, informed consent forms, and other essential documents.
  • Facilitate training and onboarding for internal and external teams involved in clinical trials.


Qualifications

  • Bachelor's degree in Life Sciences, Nursing, or a related field; advanced degree preferred.
  • Minimum of 5 years of experience in clinical project management within the biotechnology or pharmaceutical industries.
  • Comprehensive understanding of clinical trial design, regulatory requirements, and ICH/GCP guidelines.
  • Demonstrated ability to manage multiple projects concurrently in a fast-paced environment.
  • Proficiency in project management software and clinical trial management systems.
  • Exceptional communication, leadership, and inter-personal skills.
  • Strong analytical problem-solving skills and attention to detail.


Technologies & Tools

The role of Senior Clinical Program Manager will involve the use of various technologies and tools, including project management software like Microsoft Project or Monday.com, clinical trial management systems such as Medidata or Veeva Vault, electronic data capture (EDC) platforms, and statistical analysis software. Proficiency with Microsoft Office Suite is also essential for effective communication and reporting.



Ideal Candidates

The ideal candidate for the Senior Clinical Program Manager position will possess a blend of strong leadership and project management skills. They will be adept in fostering collaboration across diverse teams while maintaining a focus on achieving clinical development milestones. Successful candidates will demonstrate innovation, flexibility, and a proactive approach to problem-solving, along with a passion for advancing medical science and enhancing patient care. In addition, strong analytical capabilities and a commitment to compliance are essential attributes that will contribute to the success of the clinical program.

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