Job summary
Job post source
This job is from a recruiting firm hiring for a separate company as indicated by the consulting role and the mention of supporting a global pharmaceutical client.
Job overview
The Senior Consultant – Statistical Programming role involves leading and executing statistical programming tasks to support clinical trials and regulatory submissions, ensuring compliance with industry standards and guidelines.
Responsibilities and impact
The candidate will lead statistical programming across clinical studies, develop and validate SAS programs for data standards, generate tables and figures for reports and submissions, support data package readiness, maintain programming utilities, collaborate with biostatisticians and data managers, and ensure compliance with SOPs and regulatory requirements.
Experience and skills
Requires a Bachelor’s or Master’s degree in a relevant field, at least 10 years of statistical programming experience in pharma, biotech, or CRO, expert SAS skills including macro development, strong experience with SDTM and ADaM datasets, and excellent communication and problem-solving abilities; prior regulatory submission experience and familiarity with specific tools are preferred.
Work environment and culture
The role offers a flexible consulting position within a collaborative and supportive team environment focused on meaningful drug development projects.
Application process
Candidates are encouraged to apply directly via LinkedIn or reach out for more information.
Unique job features
This position offers the opportunity to work on high-impact clinical trial projects supporting innovative treatments in a flexible consulting capacity.
Company overview
PanaCRO is a contract research organization specializing in providing clinical trial management and support services to pharmaceutical, biotechnology, and medical device companies. The company generates revenue by offering expertise in regulatory affairs, project management, site monitoring, and data management to help clients navigate the complexities of clinical research and drug development. Founded to address the growing demand for outsourced clinical operations, PanaCRO has built a reputation for reliability, compliance with international standards, and strong client partnerships. Its history includes successful collaborations with both global and regional sponsors, emphasizing flexibility and tailored solutions. Candidates should be aware of PanaCRO's focus on quality, client-centric service, and its role in accelerating the development of innovative therapies.
How to land this job
Position your resume to showcase your extensive experience in statistical programming, emphasizing your expertise in SAS macro development, SDTM and ADaM dataset creation, and generating clinical TLFs for regulatory submissions at PanaCRO.
Highlight your leadership skills in managing multiple clinical studies and your ability to collaborate with biostatisticians and data managers, demonstrating your organizational and problem-solving capabilities.
Apply through multiple channels including PanaCRO's corporate website and LinkedIn to maximize your application visibility and ensure you reach the hiring team effectively.
Connect with professionals in the statistical programming or clinical operations divisions at PanaCRO on LinkedIn; use ice breakers such as commenting on recent clinical trial innovations or asking about their experience with CDISC standards and regulatory submissions.
Optimize your resume for ATS by incorporating keywords like 'SAS macro development,' 'SDTM,' 'ADaM,' 'clinical TLFs,' 'define.xml,' and 'regulatory submissions' to pass automated screenings with greater success.
Utilize Jennie Johnson's Power Apply feature to automate tailoring your resume, identify the best application platforms, and find relevant LinkedIn contacts, allowing you to focus your time on preparing for interviews and networking effectively.
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