Senior Biostatistician

MedFocus is a respected provider of clinical research personnel to the leading pharmaceutical and biotech companies across the U.S. We provide highly competitive salary and benefit packages, candidate referral bonuses ranging from $1000-$3000, and a client base which includes every Top-20 pharmaceutical and biotech company in the industry. Visit us at http://www.medfocus.com/ to find out more about the opportunities that we currently have available.

 

Excellent opportunity for a Senior Biostatistician in Columbus, Ohio!

 

ACCOUNTABILITY: 

 

Responsible for providing analysis and reporting of clinical trials. Requires a high degree of proficiency in ensuring accuracy and completeness across all product deliverables, while meeting these deliverables in a timely manner.  Collaborates with clients, regulatory agencies, statistical programmers, data management staff and others, as appropriate, as project biostatistician.

 

ESSENTIAL DUTIES AND RESPONSIBILITIES: 

 

- Prepare Statistical Analysis Plans; consult with sponsors regarding study design.
- Direct/collaborate with statistical programmers to derive/populate datasets and table/listing/graph outputs.
- Perform and interpret statistical analyses of data.
- Interact with medical writers to ensure appropriateness of data inferences; draft pertinent sections of a CSR or Statistical Report.
- Collaborate with data management staff to ensure accuracy and completeness of databases/file structures/coding conventions/edit checks/CRF construction.
- Interface with clients/regulatory agencies as project biostatistician.
- Attend team meetings and represent departmental needs for assigned projects.

 

MINIMUM REQUIREMENTS:

 

Education


- MA/MS or PhD in Statistics, Biostatistics or a related field

Experience
- 5 years experience in the pharmaceutical/CRO industry with a MA/MS in Statistics, Biostatistics or related field
- 3 years experience in the pharmaceutical/CRO industry with a PhD in Statistics, Biostatistics or related field

 

Skills


- Proficient SAS programming skills in performing statistical analyses and generating report ready data outputs
- Ability to understand and interpret complex mathematical/statistical problems
- Strong understanding of the clinical trial process from data acquisition to data reporting
- Ability to multitask; well developed organizational skills are requisite for an efficient performance
- Excellent interpersonal skills (written, verbal, aural); detailed oriented
- Application experience in oncology; especially survival and categorical data analysis methods (desired)