Clinical Services Project Manager

ZipRecruiter; Tucson (AZ); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading company in the life sciences and diagnostics industry is seeking a Clinical Services Project Manager in Tucson, AZ. This long-term contract role involves managing clinical testing projects, developing plans, and ensuring compliance with high standards. Ideal candidates will have a background in project management and clinical trials, with strong problem-solving skills. Benefits include healthcare, paid sick leave, and a 401k with employer match.

Benefits

Healthcare

Paid Sick Leave

401k (with 4% employer match)

Qualifications

• At least 2 years in project coordination/management in a regulated environment.
• Familiarity with clinical trial management and bio-sample handling.

Responsibilities

• Manage multiple clinical testing and lab services projects.
• Develop project plans and coordinate cross-functional efforts.
• Track and communicate project reports and clinical study data.

Skills

Problem-solving

Project Management

Clinical Trials

Education

Bachelor’s Degree

Master’s Degree

Project Management Training

Clinical Research Training

Job description

Job DescriptionJob DescriptionOur client, a leader in the life sciences and diagnostics industry, is looking for a Clinical Services Project Manager, based in Tucson, AZ.

Duration: Long term contract (Possibility of further extension)
Location: Tucson, AZ

Responsibilities:

• Manage multiple clinical testing and lab services projects from initiation to completion, serving as the primary contact for pharma clients.
  
• Develop project plans, establish timelines, and coordinate cross-functional efforts to meet project milestones.
  
• Identify gaps or bottlenecks in project plans and proactively address potential delays.
  
• Guide daily activities related to sample processing and accurate reporting of results, fostering continuous improvement within the team.
  
• Interface with external resources (e.g., CROs, site investigators, pharma clients) and manage meetings by setting agendas and taking minutes.
  
• Track and communicate project reports and clinical study data to pharma clients.
  

Required Skills:

• Problem-solving skills, knowledge of standard project management processes, and familiarity with clinical trials.
  
• Understanding of clinical sample processes, testing, quality, and regulatory compliance.
  
• Ability to manage projects under time pressure while ensuring high standards of accuracy and data quality.
  

Education:

• Bachelor’s Degree in a related field is required; a Master’s Degree is .
  
• Project Management or Clinical Research Training is required.
  
• At least 2 years in project coordination/management in a regulated environment, preferably in clinical trials, diagnostics, or the pharmaceutical industry. Familiarity with clinical trial management, bio-sample handling, and milestone-driven projects is desirable.
  

Company Benefits include: Healthcare, Paid Sick leave & 401k (with 4% employer match)

If interested, kindly send us your update resume at [e-mail]