Manager Statistical Sas Programming, Single Milano

Manager Statistical Sas Programming, Single
Milano
Lombardia, Milano

As a Manager Statistical SAS Programming in our sponsor-dedicated Flexible Solutions business unit, you and your team are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies.

This position allows you to leverage your leadership skills and participate in the development of innovative new benchmark drugs for a wide variety of therapeutic areas such as oncology, cardiovascular, respiratory, neurological, diabetes, rare diseases, pain, immunology etc.

Your expertise as a people manager in Statistical Programming has a direct impact on improving the health and lives of thousands of patients around the globe every day.

Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers!

**You can be 100% home-based in any of the EMEA locations listed on this ad - or, if you prefer, you can work from our local office in your home country.

**What else can you expect from us?

- Rewarding and meaningful work in an established, diverse, highly profitable and respected global company

- Highly competitive compensation packages

- A genuine work life balance

- Flexibility in working hours

- A thorough onboarding with support from your personal mentor

- A permanent employment contract with Labcorp Drug Development

- Excellent training and career development opportunities, as well as support with advancing your individual education

- Strong support from your Line Manager and your EMEA team, as well as from more than 20, 000 colleagues worldwide

**Your responsibilities**:

- Actively monitor staff projects quality, timelines and budgets to foresee and correct issues and assure project expectations are met

- Manage discretionary expenses and spending within your team in order to meet budget

- Work closely with lead programmers to ensure that staff resources are used efficiently, and team is well utilized

- Manage resources within your team: new hires, terminations, transfers and contractors

- Carry out line management responsibilities for your direct reports, including Performance Management and Development activities, disciplinary procedures and administrative activities.

- Encourage staff career growth and development

- Provide statistical programming support and technical support to team members

- Act as the lead programmer overseeing technical planning for increasingly complex projects including global and multiple study projects, ISS and ISE, and electronic submissions

- Participate in internal and client audits and regulatory inspections

- Proactively lead, review and amend departmental processes and documentation

- Facilitate advanced technical expertise and share your knowledge at department meetings

- Keep abreast of new statistical programming practices, methods and tools, regulatory practices and industry trends to stimulate departmental growth

**Your profile**:

- Degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc.

- In lieu of the above: an equivalent completed vocational training and / or equivalent professional experience in statistical programming

- Profound professional experience managing a team of statistical programmers working on complex clinical trials within a biotech, CRO or pharmaceutical company

- Deep knowledge in all aspects of clinical trials, from initial study set-up to study completion, with an excellent understanding of the roles and responsibilities of all related disciplines, e. g.

Biostatistics and Clinical Data Management

- Expert knowledge of base SAS, SAS macros, SAS/STAT and in debugging SAS programs

- Expert knowledge of all CDISC requirements including Reviewer's Guides and submission standards

- Excellent organizational, time management and project management skills with demonstrated leadership experience and a strong business acumen

- Outstanding problem solving and decision making skills, coupled with a proactive approach - anticipating issues and working to ensure they are avoided or resolved as quickly as possible

- Business fluency in English - both verbal and written - is a must

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.

With over 19, 000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

**Did you know?

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**Labcorp is proud to be an Equal Opportunity Employer**:

As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind.

We make employment decisions based on the needs of our business and the qualifications of