Lead Clinical Programmer. FSP Remote Based

2 weeks ago


Toronto, Canada Fortrea Full time

Join to apply for the Lead Clinical SAS Programmer role at Fortrea . 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. 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 make 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. Conduct team meetings, provide 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. Work Environment Work is performed in an office environment with exposure to electrical office equipment. Occasional drives to site locations with occasional travel both domestic and international. Physical Requirements Frequently stationary for 6‑8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. Occasional crouching, stooping, with frequent bending and twisting of upper body and neck. Ability to access and use a variety of computer software developed both in‑house and off‑the‑shelf. Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15‑20 lbs. Regular and consistent attendance. Varied hours may be required. Pay Range: CAD 110,000 - 125,000 Learn more about our EEO & Accommodations request here. Referrals increase your chances of interviewing at Fortrea by 2x. Seniority level Mid‑Senior level Employment type Full‑time Job function Information Technology #J-18808-Ljbffr



  • Toronto, Canada Everest Clinical Research Services Inc Full time

    Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical...


  • Toronto, Canada Everest Clinical Research Services Inc Full time

    Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical...


  • Toronto, Canada Everest Clinical Research Services Inc Full time

    Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical...


  • Toronto, Canada Cytel Inc Full time

    United States **and**1** more** **BE THE FIRST TO APPLY** **Who Are You?** An experienced Principal Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will lead one Phase I-IV clinical studies across your region. You are excited and enthusiastic, motivate your teams to do great work...


  • Toronto, Canada Everest Clinical Research Services Inc. Full time

    A leading clinical research organization is seeking a Project Manager to oversee clinical trials and manage project teams. The role involves ensuring project milestones are met, coordinating with sponsors, and leading cross-functional teams. Ideal candidates will have extensive experience in clinical research, strong leadership skills, and fluency in...


  • Toronto, Canada Fortrea Full time

    Principal Biostatistician – FSP (Fortrea) As an experienced Principal Biostatistician in our sponsor‑dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials for renowned, innovative, and global pharmaceutical and biotech companies. About The Team You will be part of a long‑lasting partnership...


  • Toronto, Canada Everest Clinical Research Services Inc Full time

    Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical...


  • Toronto, Canada ICON Clinical Research Full time

    A leading clinical research organization is seeking a Clinical Trial Associate focused on managing clinical supplies. The role supports the execution of clinical trials through ordering, handling, and tracking supplies while collaborating with cross-functional teams. Candidates should have relevant qualifications, extensive experience in clinical support,...


  • Toronto, Canada ICON Clinical Research Full time

    A leading clinical research organization is seeking a Clinical Trial Associate focused on managing clinical supplies. The role supports the execution of clinical trials through ordering, handling, and tracking supplies while collaborating with cross-functional teams. Candidates should have relevant qualifications, extensive experience in clinical support,...


  • Toronto, Canada Everest Clinical Research Services Inc Full time

    Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical...