R&D Contracting Management

QualStaff Resources

San Diego (CA)

Sur place

USD 48 000 - 76 000

Temps partiel

14 jours+

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Résumé du poste

QualStaff Resources in San Diego, CA is seeking a part-time Drug Development Program Manager (CMC) to support chemical and pharmaceutical development projects. The role focuses on integrated planning, governance, and cross-functional coordination within a 6-month contract.

Applicants should have 3–5+ years in pharma/biotech project environments, strong PM skills, and experience with RAID logs and tools like Planisware, MS Project, and Smartsheet.

Qualifications

  • Bachelor's degree in a related field or equivalent experience.
  • 3-5+ years supporting functional projects, processes, or operations, ideally in a pharmaceutical/biotech environment.
  • Strong program and project management skills, with experience managing multiple workstreams.
  • Experience with RAID logs and enterprise PM tools (Planisware, MS Project, Smartsheet).
  • Excellent communication and collaboration skills.

Responsabilités

  • Support integrated planning and governance for technical development projects
  • Maintain program timelines, milestones, dependencies, and risks
  • Coordinate meetings, governance activities, and follow-up actions
  • Track program risks, issues, and decisions, ensuring proper escalation
  • Partner with team members to provide visibility into project progress and risks

Connaissances

Program management
Cross-functional coordination
Communication skills
RAID logs

Formation

Bachelor's degree in related field

Outils

Planisware
MS Project
Smartsheet

Description du poste

Drug Development Program Manager - CMC(part time) – Pharmaceutical Industry

QUICK FACTS

Location: San Diego, CA, 92130

Pay range: $35.00 - $55.25 per hour

Shifts: Part-time, 24 hours per week (3 days of your choice M-Th)

Duration: 6 month Contract

EXPERIENCE/EDUCATION YOU WILL NEED
  • Bachelor's degree in a related field or equivalent experience
  • 3-5+ years supporting functional projects, processes, or operations, ideally in a pharmaceutical/biotech environment
  • Strong program and project management skills, with experience managing multiple workstreams
  • Experience with RAID logs and enterprise PM tools (Planisware, MS Project, Smartsheet)
  • Excellent communication and collaboration skills
MAIN DUTIES OF THE JOB
  • Support integrated planning and governance for technical development projects
  • Maintain program timelines, milestones, dependencies, and risks
  • Coordinate meetings, governance activities, and follow-up actions
  • Track program risks, issues, and decisions, ensuring proper escalation
  • Partner with team members to provide visibility into project progress and risks

The company is an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws.

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