•Scientifically responsible person for design and implementation of selected retrospective and observational studies; conceptualize advanced study protocols and statistical analysis plans employing up-to-date methodological and analytical techniques
•Scientifically responsible person with senior scientific "guidance/consultation" on selected studies; prepare "final quality" analysis plans and study protocols
•Draft project deliverables (reports, protocols, analysis plans, etc…) at "final quality" level with minimal to no senior review, and draft abstracts and manuscripts as lead or co-author
•As Principal Investigator, have final budget, deliverable and project timeline responsibility; identify scope expansion and need for amendments
•Support other "non-billable" activities as needed (e.g. draft and approve proposals; supervise and/or mentor junior staff; closely collaborate with other business units; lead some efforts as company representative)
•Comfortable with client and/or study sponsor communications
•Excellent organizational and communication skills, both written and oral, with attention to detail
•Ability to communicate effectively with peers and senior managers
•Experience in clinical research, including site recruitment, training and management, IRB approval process, and CRF development preferred
•Desirable to have strong analytical/statistical skills and proficient in statistical programming software (e.g., SAS)
Education and Experience
•PhD with two years of experience; or Masters with greater than five years of experience; or Bachelors with greater than seven years of experience plus relevant coursework
Competent in written and spoken English.
MS Word, PowerPoint, Excel; should have familiarity with data analysis software (e.g., SAS) mainly for the purpose of quality control.
HOW TO APPLY:
In addition to completing your online profile and applying for the position of interest here on our careers page, please email your resume or CV and cover letter to firstname.lastname@example.org with the position title in the email subject line. Thank you!
We are an Equal Opportunity Employer, M/F/D/V
United BioSource Corporation - 11 months ago