Job Description

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. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.


Joining Fortrea's Clinical Data Management sponsor dedicated team will offer a rewarding career, a chance to work in an energetic & team-oriented workplace and exposure within a world-leading team.


The Lead Clinical SAS Programmer role is a great opportunity to work within our sponsor dedicated department and have this unique relationship with a sponsor. You will focus on

development and implementation of programming solutions

to address global technical services issues and optimize clinical data processes.

Your responsibilities

Expected to assist with leading EDC Builds and mentor the study team in SAS or other proprietary software. Lead the development of visual analytics dashboard using tools like Spotfire/Tableau. Functions as Subject Matter Expert (SME) and Lead on multiple projects. Assist in the development and implementation of solutions to global technical service issues and concerns regarding SAS or other proprietary software, including proactive prevention strategies. Co-ordinate activities of all programmers across projects and provide technical/functional expertise and makes programming decisions/recommendations at study or project level. Develop/validate Custom/Complex Edit-Check programs, reports, and efficiently handle external data and data reconciliations. Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, working within budget, meeting timelines, maximizing quality, interaction with other departments and the client, etc. With assistance meet with Data Manager on assigned projects to discuss technical strategies, contractual obligations, and timelines. Provide information on resource needs as appropriate. Conducts team meetings, provides technical guidance/assistance to Programmers, and perform other duties as assigned by Manager. And all other duties as needed or assigned

Education:

Bachelor's degree (life sciences, health sciences, information technology or related subjects preferred). Experience and/or education plus relevant work experience, equating to a bachelor's degree will be accepted in lieu of a bachelor's degree. Fluent in English, both written and verbal. Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Experience:

7 to 9 years of relevant work experience to include data management programming activities including SAS Programming Demonstrate excellent problem-solving skills, a proactive approach, and the ability to make sound decisions. Demonstrated skill in leading teams, by example and mentoring staff. Excellent oral and written communication and presentation skills. Knowledge of clinical trial process and data management, CRF design, and systems applications to support operations. Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical/biotechnological companies. Demonstrated ability to work in a team environment. Demonstrated ability to handle multiple competing priorities.

What you can expect from us

Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc. A genuine work life balance Flexibility in working hours A thorough onboarding with support from your personal mentor A permanent employment contract with Fortrea and a rewarding career progression

Position is based remote in Canada


This position is not eligible for sponsorship.


Pay Range: CAD 110,000 - 125,000


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