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Clinical Services Project Manager I
Job Location:
Job Location:
Tucson, AZ - USA
Monthly Salary:
Not provided by the employer
Monthly Salary:
Posted:
21 October 2026 (4 hours ago)
Posted:
Application Deadline:
18 January 2027
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Job Title: Clinical Services Project Manager I
Job Location: Tucson AZ (Remote)
Job Duration: 11 months on W2
Job Description:
Job Summary
Manages low- to medium-complexity clinical and lab services projects from initiation to completion ensuring delivery on time within budget and in compliance with pharma services plans. Acts as the primary point of contact for Pharma and Roche clients.
Key Responsibilities
Qualifications & Requirements
Job Location: Tucson AZ (Remote)
Job Duration: 11 months on W2
Job Description:
Job Summary
Manages low- to medium-complexity clinical and lab services projects from initiation to completion ensuring delivery on time within budget and in compliance with pharma services plans. Acts as the primary point of contact for Pharma and Roche clients.
Key Responsibilities
- Project Management: Oversee multiple clinical testing and lab services projects establishing timelines tracking cross-functional activities and identifying potential bottlenecks.
- Client & External Relations: Serve as the primary single point of contact for Pharma customers CROs and site investigators.
- Sample & Data Oversight: Guide day-to-day sample process flow ensure accurate result reporting and track/communicate project reports and clinical study data.
- Administrative & Collaboration: Manage meeting agendas minutes and foster continuous improvement within the clinical sciences team.
Qualifications & Requirements
- Education: Bachelors Degree in a related field (or equivalent experience). Masters degree and Project Management/Clinical Research certifications are preferred.
- Experience: 2 years of project and/or clinical trial management experience in a regulated CRO diagnostic or pharmaceutical environment.
- Experience with rapid milestone achievement and bio-sample management is preferred.
- Strong problem-solving leadership and interpersonal communication skills.
- Familiarity with clinical trials quality/regulatory processes and sample process flow.
- Proficiency in standard office software (Word Excel email) and ability to work effectively under time pressure.
- Experience with Agile methodologies preferred
Required Experience:
IC
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