Job summary
Job post source
This job is directly from ClinChoice
Job overview
The Senior Real World Statistics role at ClinChoice involves leading statistical work on observational studies and clinical trials to support drug development and market access, impacting study quality and outcomes.
Responsibilities and impact
The role includes designing and analyzing observational studies, reviewing study protocols and data, collaborating with cross-functional teams, supporting documentation development, and contributing to reports and publications.
Experience and skills
Requires a Master or PhD in Biostatistics or related field with 3-7 years experience, including 2 years on observational studies and 3 years of SAS and R programming skills; strong analytical, communication, and teamwork abilities are essential.
Career development
ClinChoice emphasizes professional development through continuous training and close management to maintain high competence and expertise, supporting career growth within a global CRO environment.
Work environment and culture
ClinChoice promotes a collaborative, quality-focused, diverse, and inclusive culture with a strong work-life balance and low turnover rates, valuing employees as key assets.
Company information
ClinChoice is a global full-service CRO with over 28 years of experience, 4,000 professionals worldwide, specializing in clinical development and functional solutions for pharma, biotech, medical devices, and consumer health sectors.
Job location and travel
The position is remote, allowing flexible work location.
Application process
Applicants submit a CV, receive acknowledgment, and if qualified, are invited for a phone interview; due to volume, only successful candidates are contacted further.
Unique job features
The job offers the opportunity to work on diverse real world data projects with cross-functional teams in a dynamic, fast-paced environment, emphasizing strategic input and expert guidance.
Company overview
ClinChoice is a global clinical research organization that provides comprehensive clinical development and consulting services to the pharmaceutical, biotechnology, and medical device industries. They make money by offering services such as clinical trial management, regulatory consulting, data management, and biostatistics to support the development and approval of new medical products. Founded in 1995, ClinChoice has grown through strategic acquisitions and partnerships, expanding its global footprint and capabilities to deliver high-quality, cost-effective solutions for their clients.
How to land this job
Position your resume to highlight expertise in real world observational studies, with emphasis on your experience in study design, statistical analysis, and critical review of protocols and data, aligning with ClinChoice’s focus on drug development and real world evidence.
Emphasize your proficiency in SAS and R programming, your knowledge of the US healthcare system, and your ability to collaborate effectively across cross-functional teams including Health Economics, Medical Affairs, and Clinical Development.
Apply through multiple channels such as ClinChoice’s official corporate careers page and LinkedIn job postings to maximize your application visibility and increase chances of being noticed.
Connect on LinkedIn with professionals working in ClinChoice’s Real World Statistics or Global Medicines Development teams; start conversations by referencing recent ClinChoice projects or expressing genuine interest in their collaborative, quality-focused culture.
Optimize your resume for ATS by incorporating keywords from the job description like 'observational studies,' 'real world data,' 'SAS,' 'R programming,' 'cross-functional collaboration,' and 'statistical analysis' to ensure your resume passes initial automated screenings.
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