Clinical Project Manager IV at Roche
Tucson, Arizona, USA -
Full Time


Start Date

Immediate

Expiry Date

07 Sep, 25

Salary

252700.0

Posted On

08 Jun, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Research, Facilitation, Design Control, Communication Skills, Ms Project, Regulated Industry, Pharmaceutical Industry, Stakeholder Management, Clinical Operations

Industry

Pharmaceuticals

Description

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
The Position
A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.

THE OPPORTUNITY

Roche is seeking a very talented Clinical Project Manager who is responsible for partnering with key stakeholders and CDMA (Clinical Development & Medical Affairs) functions to manage CDMA related project information to support decision making by: CDMA Project Teams, CDMA Leadership (Chapter & Sub-Chapter), respective Customer Area’s (CAs) and Project Teams (PTMs). This person will apply project management skills and clinical operations experience to ensure on-time delivery of CDMA-related deliverables, within budget and with high customer satisfaction. Projects may be complex; may involve collaboration with other Clinical Project Managers, other PMO Project Managers, and/or PMO leadership.

Responsibilities
  • Ensure proactive alignment for planning and reporting CDMA-related project information with local and global CDMA team members, their respective CDMA leadership, and global PMs for making informed decisions.
  • In collaboration with the Functional Partner (FP) and Sub-Chapter Leads (SCLs), ensure the tactical coordination of the CDMA’s clinical study budget planning and reporting processes.
  • Integrated planning of CDMA resources, expenditures, and timeline within project budgets;
  • Identifies clinical study gaps, potential bottleneck,s and/or delays based upon the overarching project’s planning assumptions;
  • Oversees CDMA-related Risk Management topics, including critical path, risk assessments, scenario creatio,n and analysis;
  • Collaborates with CDMA project team members and leadership to identify, propose, and implement solutions that mitigate clinical study-related gaps and delays to get the project back on schedule according to plan;
  • Compiles, tracks, and reports real-time data for Change Management, Resource Management, and Risk Management across the entire CDMA Clinical Study portfolio.
  • Ensures consistent and transparent communication across the CDMA stakeholders, the PPMs, and the Project Teams.
  • Independently manages meetings to include setting agendas, organizing meeting time,s and editing meeting minutes.
  • Miscellaneous duties and special projects as assigned.
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