ClinChoice is a global full-service CRO committed to professional growth and a quality-driven “one-team” culture. We are seeking a Principal Statistician to join our in-house team and support projects across a diverse client portfolio, including pharmaceutical, biotechnology, medical device, and consumer health companies of varying sizes. We are seeking a highly skilled Principal Statistician to lead statistical activities for clinical trials. This role requires hands-on statistical expertise, strong communication skills, and the ability to independently lead projects while collaborating closely with cross-functional teams. Join our team: you can be part of making a difference in peoples' lives and experience a fulfilling and rewarding career! <h3 style="line-height: 1.2;" data-start="694" data-end="720">Key Responsibilities</h3> <ul data-start="721" data-end="1606"> <li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="721" data-end="833"> Lead and provide statistical support for clinical studies.  </li> <li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="834" data-end="940"> Act as the lead statistician on assigned studies, overseeing statistical strategy and deliverables </li> <li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="941" data-end="1136"> Author and review key statistical documents, including: <ul data-start="1001" data-end="1136"> <li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1001" data-end="1038"> Statistical Analysis Plans (SAPs) </li> <li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1041" data-end="1083"> Analysis Database Specifications (ADS) </li> <li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1086" data-end="1136"> Statistical sections of clinical study reports </li> </ul> </li> <li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1137" data-end="1233"> Review and interpret analysis outputs, ensuring accuracy, quality, and regulatory compliance </li> <li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1234" data-end="1342"> Collaborate with cross-functional teams including Clinical, Programming, Data Management, and Regulatory </li> <li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1343" data-end="1414"> Provide guidance and oversight to statistical programmers as needed </li> <li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1415" data-end="1528"> Communicate statistical concepts, results, and risks clearly to both technical and non-technical stakeholders </li> <li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1529" data-end="1606"> Ensure adherence to regulatory standards (FDA, ICH, GCP) and company SOPs </li> </ul> <h3 style="line-height: 1.2;" data-start="1608" data-end="1637">Required Qualifications</h3> <ul data-start="1638" data-end="2205"> <li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1638" data-end="1700"> MS or PhD in Statistics, Biostatistics, or a related field </li> <li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1638" data-end="1700">There are no specific therapeutic area requirements; however, experience in Oncology, Rare Disease, or Neuroscience would be advantageous.</li> <li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1638" data-end="1700">Strong oral and written communication skills, with the ability to effectively communicate internally and with clients.</li> <li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1638" data-end="1700">Demonstrated understanding and insight in statistics, drug development process, and relevant FDA regulations.</li> <li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1638" data-end="1700">Pharmaceutical, CRO, or related industry experience with clinical trials, including interaction with Regulatory Agencies, especially the FDA.</li> </ul> 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 <span style="font-family: tahoma, arial, he

Principal Statistician - Permanent Role -Remote in UK