Clinical Project Manager IV

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.

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.

In this role, you will:

* 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.

Who you are

Formal Training/Education:

• BS/BA in science, engineering or business administration OR equivalent combination of education and work experience.

• Master's degree preferred.

• Life Sciences or Engineering/Technical field of study preferred.

• Project Management specific training and/or certification preferred.

Experience:

• 8+ years project management, product development, and/or relevant experience

• Experience working in research & development.

• Experience working in clinical operations.

• Experience working in a regulated Industry.

Knowledge, Skills, and Abilities:

• Successful problem-solving skills and the ability to coordinate project-related activities

• Excellent written and oral communication skills

• Advanced stakeholder management, facilitation, and negotiation skills

• Proficient in MS Project and/or Project & Portfolio Management Tool

• Ability to manage projects with ambitious milestones in high-pressure circumstances

• Ability to manage projects with activity/milestone achievement to launch the product.

• Ability to escalate and drive management decisions in relation to project execution and resource needs

• Diagnostic, Medical Device, Pharmaceutical industry, and/or relevant diagnostic area knowledge preferred

• Understanding of relevant Design Control and/or Phased Development processes preferred

Travel requirements

• Some domestic/international travel may be required

This opportunity needs to be based onsite at one of the locations below:

Tucson, Arizona
Pleasanton, California
Indianapolis, Indiana
Penzberg, Germany
Mannheim, Germany
Rotkreuz, Switzerland

The expected salary range for this position, based on the primary location of Arizona, and Indiana is $118,300 - 219,700, California is $136,100 - 252,700 of the hiring range. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.

Benefits

A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let's build a healthier future, together.

Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

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