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 Sr. Data Manager (DM) is responsible for the development, execution and oversight of all data  management plans, deliverables, and processes on assigned projects. The DM serves as the subject matter expert and  primary interface between global Study Teams and Biostatistics groups, local study teams and/or CRO’s relative to all data within specific studies, databases, and/or electronic data  capture (e-DC) and case report form (e-CRF) applications and systems. The DM leads and oversees data management activities including CRF and database development based on study protocols and needs, periodic data  quality checks, data queries, data cleaning and discrepancy management. Coordinates the formatting and storage of  study data per study protocol, SOP, area work instructions and post-production change management to maintain high  quality data records.

The Opportunity

The DM works with Study Managers and Clinical Research Associates to provide both in-house and on-site user training and secondary user support, as required on individual studies. The DM supports Quality and Regulatory compliance initiatives on all projects, and handles the coordination of change requests during the life-cycle of study data handling tools. Specialized and in-depth comprehensive knowledge and experience in a particular field, or business area. Duties are  varied and complex, often involving research, analysis and solution development. Provides direction on issues of area  of expertise and assist department leadership in setting strategic direction. Requires the regular use of originality and ingenuity. Plans, conducts and oversees work involving the largest  and most important/complex projects. Does not supervise, but provides direction to team on projects and  assignments. Works with minimum supervision. Reviews progress with management. 

Responsible  for  maintaining  and  continuously  improving  the  quality  system  and  achieving  quality objectives through daily actions. 

Other key responsibilities include:

• Guides and advises study teams on the definition of the  data management and the study management in the paper and/or electronic systems. 

• Reviews protocol on clinical/technical data management and system implications. 

• Creates clinical data management plan. 

• Collaborates globally as needed on the design, documentation, testing and implementation of clinical data studies. 

• Ensures the use of standards and alignment of data management when supporting studies. 

• Uses tools and provides guidance in order to execute timely data reconciliation, data cleaning, and data analysis. 

• Responsible for timely delivery of clean, complete high quality data for analysis. 

Who you are

• Bachelor’s degree in life science/Laboratory, computer science or related field 

• 1-2 years’ experience in data management and analysis, study management and reporting of clinical study results 

• Experience in database design, construction and verification/validation 

• Demonstrated leadership skills in coordinating data workflow within clinical studies, 

• Ability to work in an efficient and collaborative fashion with multi-disciplinary teams 

• Strong communication and interpersonal skills

Relocation benefits are not available for this posting

The expected salary range for this position based on the primary location of Indiana is $71,800 - $133,400. 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

Who we are

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.

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.