Job summary
Job post source
This job is from a recruiting firm hiring for a separate company as it mentions supporting high-profile pharmaceutical clients and is a consulting role.
Job overview
The Director Level Statistician Consultant role involves providing expert statistical leadership and strategic input for clinical trials and regulatory submissions in the pharmaceutical industry.
Responsibilities and impact
The consultant will lead statistical design, conduct, analysis, and reporting of clinical studies, author and review regulatory submission documents, collaborate with cross-functional teams, and ensure compliance with industry standards and regulatory requirements.
Experience and skills
Candidates must have a PhD in Statistics or related field and at least 10 years of pharmaceutical or biotech industry experience, with proven success in regulatory submissions and strong knowledge of statistical methodologies and guidelines.
Work environment and culture
The role offers flexible consulting work within a dedicated team focused on innovative drug development and public health advancement.
Job location and travel
The position is remote within the U.S., allowing flexible work arrangements.
Unique job features
The job provides a flexible consulting opportunity to apply deep statistical expertise in impactful drug development projects supporting regulatory submissions.
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
Tailor your resume to emphasize your Ph.D. in Statistics or Biostatistics and highlight over 10 years of pharmaceutical or biotech industry experience, focusing on clinical development and regulatory submissions.
Showcase your expertise in authoring statistical analysis plans, reviewing tables/listings/figures, and contributing to regulatory submission documents, underlining your leadership in study design and statistical methodologies.
Apply through multiple channels including PanaCRO's corporate careers page, LinkedIn job postings, and specialized pharmaceutical consulting platforms to maximize visibility.
Connect with current statisticians or consultants in the clinical development division at PanaCRO on LinkedIn; initiate conversations by referencing recent regulatory submissions or asking about collaboration across cross-functional teams.
Optimize your resume for ATS by incorporating keywords like 'statistical leadership,' 'regulatory submissions,' 'clinical trial design,' 'ICH guidelines,' and 'FDA/EMA compliance' to ensure it passes automated screenings.
Utilize Jennie Johnson's Power Apply feature to automate tailored applications, identify multiple application portals, and find relevant PanaCRO contacts on LinkedIn, saving you time and boosting your chances of landing the role.
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