Apply for this job now

Remote Clinical Data Programmer (Ref: RM)

Location
United States
Job Type
Permanent
Posted
7 Sep 2022
THE COMPANY PHASTAR is a multiple award-winning global biometric Contract Research Organization (CRO) that is accredited as an outstanding company to work for by Best Companies. We partner with pharmaceutical, biotechnology and medical device organizations to provide the expertise and processes to manage and deliver on time, quality biostatistics, programming, data management and data science services. With offices across the UK, US, Germany, Kenya, Australia, India, China and Japan, PHASTAR is the second largest specialized biometrics provider globally, and the largest in the UK. Our unique approach to data analysis, "The PHASTAR Discipline", has led us to build a reputation for outstanding quality. With this as our core focus, we're looking for talented individuals who share our passion for quality and technical expertise to join our team. WHY PHASTAR Accredited as an outstanding company to work for, PHASTAR is committed to employee engagement, workplace satisfaction and ensuring a healthy work-life balance. We offer flexible working, part-time hours, involvement in developing company-wide initiatives, structured training and development plans, and a truly supportive, fun and friendly environment. What's more, when you join our team, PHASTAR will plant a tree in your honour, as one of our Environmental, Social and Governance (ESG) initiatives. So, not only would you get your dream job, you'll also be helping to save the planet! THE ROLE Demand for our Functional Service Provision is growing, and we are looking for a Clinical Data Programmer with SAS and EDC expertise. As a Clinical Data Programmer, you will be fully integrated into our sponsor's data management team. Responsibilities include: Creating data cleaning reporting solutions with appropriate oversight that support the quality and timely delivery of data cleaning, study status metric, and monitoring reports and visualizations required per standard and study specific data review plans Creating any needed documentation for reports throughout the lifespan of the study and/or asset for all Clinical Data Reporting Services deliverables Skills and Experience Required: BSc, MSc or PhD in mathematics, science or IT related discipline 4-5 years experience working as a SAS statistical programmer Extensive EDC experience Advanced knowledge of medical terminology, clinical trial methodologies, and FDA/ICH regulations Ability to work independently with minimum oversight Excellent written and verbal communication skills APPLY NOW With the world's eyes focused on clinical trial data, this is a fantastic time to join an award-winning specialized biometric CRO that is renowned for its technical expertise, outstanding quality and cutting-edge data science techniques. We offer flexible working, part-time hours, structured training and development plans, continuous learning opportunities, and a competitive salary and benefits package. We're committed to ensuring our employees achieve a healthy work-life balance, within a supportive, fun and friendly working environment. Should you feel that you have the right skill set and motivations for this position, please apply! Please note that we are considering candidates located anywhere in the US as this role can be carried out remotely. PHASTAR does not accept any CVs received from recruitment agencies. In the event that speculative CVs are submitted by recruitment agencies, PHASTAR reserves the right to contact these candidates directly and consider them for current/future vacancies without any financial obligation to the recruitment agency in question. This applies to any CVs sent directly to any PHASTAR employee.
Apply for this job now

Details

  • Job Reference: 705891689-2
  • Date Posted: 7 September 2022
  • Recruiter: PHASTAR
  • Location: United States
  • Salary: On Application
  • Sector: I.T. & Communications
  • Job Type: Permanent
  • Start Date: Mon, 05 Sep 2022 05:45:00 EST