Remote Jobs

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Senior PKPD Programmer Consultant (remote in US)

ClinChoice

Location
United States of America
Posted

Senior PKPD Programmer Consultant job at ClinChoice: Develop SAS programs for clinical trials, provide QC oversight, and troubleshoot technical issues in a supportive culture.

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Salary Range
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Senior SDK Engineer

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Support Engineer (Remote, Australia)

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Location
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Salary Range
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Software Engineer in Test III

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Location
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Emburse logo

Software Engineer in Test III

Emburse

Location
Spain
Posted

Software Engineer in Test IIISpainEPD – Engineering/Prod Dev /Full-Time /Hybrid at Emburse

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Technical Working Student – 100% Remote

Giant Swarm

Location
Germany
Posted
Salary Range
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ClinChoice logo

Senior PKPD Programmer Consultant (remote in US)

ClinChoice

Job Summary

ClinChoice is seeking a Senior PKPD Programmer Consultant to join one of their clients focused on developing novel cell-based cancer therapies. The ideal candidate will have 5+ years of experience in statistical programming with clinical data and SAS, as well as expertise in PK/PD area, CDISC, and regulations. As a client-facing role, the consultant will work independently while establishing high-trust relationships with clients. Responsibilities include developing, validating, and maintaining SAS programs for data analysis, providing QC oversight, and troubleshooting technical issues. ClinChoice offers a supportive culture, flexible remote work options, and opportunities for professional development. The company is an equal opportunity employer with a strong focus on diversity and inclusivity.

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….

ClinChoice is searching for a Senior PKPD Programmer Consultant to join one of our clients and they focused on the development of novel cell-based cancer therapies. 

ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.  

RESPONSIBILITIES

  • Develop, validate and maintain SAS programs for data analysis in translational and early phase clinical trials
  • Responsible for providing QC oversight of CRO deliverables like ADaMs, and tables, listings and figures
  • Independently develop SAS or other programs and specifications for production of output to support study needs including publications, ad hoc analyses in a timely fashion
  • Demonstrate expertise in SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT & SAS/GRAPH.
  •  Independently verify other programmers’ results
  • Adhere to company SOPs and department guidelines
  • Work concurrently on multiple projects
  • Troubleshoot technical and project issues
  • Help with infrastructure development of the department
  • Communicate effectively with internal cross-functional groups and external partners

QUALIFICATIONS

  • BS/BA degree in related discipline
  • At least 5 years of experience in statistical programming with clinical data and SAS
  • Experience in PK/PD area strongly preferred
  • Strong SAS programming skills required with proficiency in SAS/Base, SAS/Stat and SAS/Macros
  • CDISC proficiency required
  • SAS/GRAPH experience desirable
  • Knowledge of appropriate regulations, industry standards and guidance documents
  • Uses broad expertise or unique knowledge and skills to contribute to development of company objectives and principles, and to achieve goals in creative and effective ways
  • Good interpersonal communication skills to collaborate effectively with internal cross-functional groups and external partners

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

Who will you be working for?

About ClinChoice

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.           

Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology.   The success of these core values is evidenced by our below industry average turnover rates.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.


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