ClinForce recognizes that the skills and experience of our personnel are our strongest asset. It’s because we work with the brightest and most talented professionals in the industry that many of the world’s leading pharmaceutical, biotechnology and device companies rely on us for their staffing and project outsourcing needs.

When you contact ClinForce you gain immediate exposure to rewarding positions with leading research companies across the U.S. More than two decades of building relationships with the most reputable organizations in the clinical trials industry enables us to match your skills and objectives with exciting and rewarding contract or direct hire opportunities. We form long-lasting relationships with our associates and work hard to ensure their satisfaction, including competitive compensation and a comprehensive benefits package.

ClinForce offers rewarding opportunities across all clinical disciplines including:


Job Detail View
Job Title: Statistical Programmer
Job Number: 220-2607
Company ClinForce
Skill Sets: Long term contract assignment; MS preferred
City: Upper Providence
State: PA
Region:
Pay Rate:
Recruiter: Catherine Zeier
Job Company:
Job Description: Successful candidate will provide programming expertise (SAS) in the production of analyses, tabulations, graphics and listings from clinical trial data. Key responsibilities and skills include the following:
  • Contribute to the preparation of analysis plans
  • Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrated clinical statistical reports, etc.
  • Contribute to the integrated clinical/statistical report and other similar documents
  • Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming and reporting
  • Perform QC/QA procedures on work performed


    Job Detail View
    Job Title: Statistical Programmer
    Job Number: 208-5639
    Company ClinForce
    Skill Sets: MS degree in Biostatistics or related field; 3 years related experience within the Contract Research Organization (CRO) or pharmaceutical/clinical trials environment
    City: King of Prussia
    State: PA
    Region:
    Pay Rate:
    Recruiter: Holly Price
    Job Company:
    Job Description: Successful candidate will provide statistical programming expertise (preferably in SAS) in the production of analyses, tabulations, graphics and listings from clinical trial data. Key responsibilities and skills include, but are not limited to the following:
  • Contribute to the preparation of analysis plans
  • Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrated clinical statistical reports and other similar reports
  • Contribute to the integrated clinical/statistical report and other similar documents
  • Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming and reporting
  • Perform quality assurance procedures on work performed by others


    Job Detail View
    Job Title: Statistical Programmer
    Job Number: 220-2634
    Company ClinForce
    Skill Sets: 3+ years experience within the clinical research industry; MS Degree required; Experience in reporting of clinical trials data in pharmaceutical industry using SAS is extremely important; Must have good communication skills; Experience with ISS and ISE reporting is helpful
    City: King of Prussia
    State: PA
    Region:
    Pay Rate:
    Recruiter: Catherine Zeier
    Job Company:
    Job Description: Successful candidate will provide programming expertise (SAS) in the production of TLGs from clinical trial data. Key responsibilities include the following: contribute to the preparation of SAPs, prepare/document and test required programs and procedure data displays for inclusion in integrated clinical statistical reports, etc. Contribute to the integrated clinical/statistical report and other similar documents. Ensure analysis data and programming code meet regulatory and company standards. Perform QC/QA procedures on work performed by others.

    ClinForce has the most experienced and knowledgeable recruiting staff in the industry