Clinical Project Manager IV
Clinical Project Manager IV
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$ 118300 - 219700
1 Vacancy
Job 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. Its 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. Thats 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 Areas (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 CDMAs clinical study budget planning and reporting processes.
Integrated planning of CDMA resources expenditures and timeline within project budgets;
Identifies clinical study gaps potential bottlenecks and/or delays based upon the overarching projects planning assumptions;
Oversees CDMA-related Risk Management topics including critical path risk assessments scenario creation 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 times 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.
Masters 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 $118300 - 219700 California is $136100 - 252700 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.
Who we are
A healthier future drives us to innovate. Together more than 100000 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.
Lets 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 companys 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.
If you have a disability and need an accommodation in relation to the online application process please contact us by completing this form Accommodations for Applicants.
Required Experience:
IC
Employment Type
Full-Time
