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| Company: |
Smith Hanley Consulting Group Florida |
| Base Pay: |
N/A |
| Other Pay: |
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| Employee Type: |
Full-Time |
| Industry: |
Biotechnology
Pharmaceutical |
| Manages Others: |
No |
| Job Type: |
Biotech
Pharmaceutical |
| Required Education: |
Not Specified |
| Required Experience: |
Not Specified |
| Required Travel: |
Not Specified |
| Relocation Covered: |
Not Specified |
| Reference ID: |
70144 |
| Location: |
 US-PA-Warrington
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| Contact: |
Not Available |
| Phone: |
Not Available |
| Email: |
Send Email Now |
| Fax: |
Not Available |
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Our Commitment
We are committed to our relationships with our clients, candidates, and consultants, as well as to one another and our communities. We hope our dedication to these relationships shines through with the partnerships we nurture daily. To achieve success in all facets, we value trust, communication, customer service, and diversity.
We demonstrate our commitment to diversity by recruiting from all backgrounds, cultures, and ethnicities. We recognize the unique differences each employee brings to the company and we support environments that encourage diversity, believing that it adds value to the organization. This value is evident in every aspect of the organization: new ideas and perspectives, motivation, buy-in, retention, and new sources of talent. By valuing differences, we affirm our dedication to treating everyone with fairness and respect.
Learn More about Smith Hanley Consulting Group Florida
Visit Our Website
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The Biostatistician will be responsible for the following duties, among others:
• Provides input on design of studies and reviews protocols
• Computes sample sizes in conjunction with clinical staff as required for clinical studies
• Writes detailed analysis plans and analyzes clinical data, as directed by immediate supervisor
• Designs summary tables, reports, and graphs for presentation of results
• Writes statistical analysis descriptions for protocols and final reports, as directed by immediate supervisor
• Consults with others in company on statistical issues when requested
• Creates and modifies, or directs the creation and modification of SAS programs to support all of the above
• Maintaining statistical and programming activities and documentation in accordance with Company's policies, procedures and all standard operating procedures (SOPs)
• Maintaining thorough knowledge of all Company systems, utilities and other tools
• Masters or PhD in biostatistics or statistics is required
• At least 5 years of pharmaceutical industry experience with Masters Degree; at least 3 years of pharmaceutical industry experience with PhD
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