AddressRoche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people’s varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join Roche, where every voice matters.
The Position
Always innovating, we bring together dedicated people and diverse perspectives from across our global network, empowering each other to keep breaking new ground. We are Roche.
Your Opportunity
As Clinical Services Project Manager, you will manage clinical and lab Services Projects from initiation through contract completion by applying project management skills and experience in delivering projects on time, within budget and with high customer satisfaction. You facilitate cross-functional interactions to complete the assigned projects within the deadline. Also, you are
- Managing clinical testing and lab Services Projects collaboratively, from initiation through contract completion.
- Performing tactical coordination of timelines for all projects and functions within CDx Pharma Services such developing project plans, establishing and coordinating timelines for assigned projects and functions; managing execution of cross-functional plans and tracking the progress of activities; identifying gaps, potential bottlenecks or delays and challenge assumptions and propose options to close gaps
- Oversees and guides day-to-day activities of sample process flow and accurate reporting of results. Implements best practices within the clinical sciences team; fosters continuous improvement by ensuring knowledge and experience exchange.
- Guides and manages cross-functional interactions to complete the assigned projects within the deadline.
- Interface with resources outside of the company (Contract Research Organizations (CROs), site investigators, client counterparts, etc.) and serves as single point of contact with Pharma and Roche clients.
- Completing miscellaneous duties and special projects as assigned.
Who you are
Required
- You hold a Bachelor's Degree in a related field or equivalent combination of education and relevant work experience.
- You bring 2 years experience of project and/or clinical trial coordinator/management experience in a regulated, CRO, diagnostic, and/or pharmaceutical industry with regulated documentation
Preferred
- You hold a Master's Degree in a related field and/or Specific Project Management Training, or Clinical Research training and/or certification
- Your experience is in clinical trial management and knowledge of bio-sample (clinical testing) management and process flow in the Diagnostic and/or Pharmaceutical industry
- Previous experience with standard project management process (PMI) .
Behaviors, competencies, and qualities of the ideal applicant.
- Understanding of Quality and Regulatory processes.
- Knowledge of clinical sample process flow and testing.
- Proficiency with word processing, spreadsheet, database, and email software (e.g., Microsoft Excel, Microsoft Word).
- Ability to apply specialized knowledge and skills in functional areas, particularly interfacing with laboratory, scientific and medical staff.
This is remote position. Relocation benefits are not offered for this posting.
Who we are
At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.
Ventana Medical Systems, Inc. (Ventana), a member of the Roche Group, innovates and manufactures instruments and reagents that automate tissue processing and slide staining for cancer diagnostics. Our integrated staining, workflow management and digital pathology solutions optimize laboratory efficiency to reduce errors and support diagnosis for pathology professionals. Together with Roche, Ventana is driving personalized healthcare through accelerated drug discovery and companion diagnostics.
Roche is an equal opportunity employer and strictly prohibits unlawful discrimination based upon an individual’s race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other characteristic protected by law.
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.
