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We currently have job opportunities:

  • Biostatistician
  • SAS Programmer
  • Clinical Research Associate
  • Clinical Data Coordinator
  • Clinical Data Manager

BioInforMedica, Inc. also places Clinical Research Coordinators (CRC's), Research Scientists, Regulatory staff, Outcomes staff, Medical Writers, Database Administrators (DBA's), and many other pharmaceutical specialties. To better serve you, please fill out the Candidate Form and review the List of Recent Job Opportunities.


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List of Recent Job Opportunities:

Biostatistician

Position title will be based on experience level of candidate and range from junior to senior levels. Responsible for statistical aspects of pre-clinical through Phase IV clinical trials, including experimental design, protocol development, statistical analyses, writing statistical contributions to clinical reports and collaborating with clinical investigators, physicians and medical writers. Serve as a consulting statistician for various teams, play a key role in preparing research reports and NDA submissions for various drugs. Many therapeutic areas, including CNS, GI, Oncology, Cardio, Respiratory and HIV/AIDS.Very good oral and written communication and negotiation skills.

Minimum Requirements: MS plus 2 - 9 years experience or a PhD with 0 - 5 years experience. Degree must be in statistics or in mathematics with a large statistical component.
*Level and title will be commensurate with the education and experience level of the selected candidate.

22 positions available

SAS Programmer

Positions range from junior to senior levels. Responsible for editing and validating programs using SAS macros to generate listings and tables for the study reports and NDA submissions, data step manipulations for data quality assurance/validation of table, listing and summaries, using SAS to analyze clinical data from CRF's creating SAS data sets for the purpose of analysis and report writing for clinical trials (Pre-clinical through Phases IV), generating efficacy and safety reports, creating datasets and generating reports using PROC Tab, PROC Report, Data Null, SAS arrays, PROC SQL and Macros, and verify and document programs.

Minimum Requirements: BS in computer science, mathematics or other scientific field (or equivalent theoretical/technical depth).
3-5 years (10 years for Director, Statistical Programming) experience   programming and analyzing scientific data, preferably in a pharmaceutical/clinical trial environment. Expertise in SAS programming language with a knowledge of relational databases, medical terminology and understanding of clinical research process. Level and title will be commensurate with the education and experience level of the selected candidate.


6 positions available

Clinical Research Associate

Positions range from junior to senior levels with regional opportunities in addition to in house positions.
Responsibilities include conducting Phase I - IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior staff in planning study conduct, designing case report forms (CRF's), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions. Responsible for writing basic study protocols, monitoring or overseeing monitoring of investigational sites to ensure protocol adherence, assuring timely enrollment of patients and retrieval of CRF's from study sites, processing CRF's including data cleanup and classification of data, and completion of study summary.
Bachelor's Degree preferred with previous pharmaceutical research experience. Bachelors of Science in Nursing recommended.

5 positions available

Clinical Data Coordinator

Clinical Data Coordinator (CDC) performs routine data management activities during the maintenance phase of clinical studies. Duties include, but are not limited to, data cleaning, query tracking, coding of medical terms, and quality control checks. Perform data management tasks including: · Performing visual review of CRFs. · Executing data checking programs, reviewing listings, and investigating discrepancies. · Generating and tracking data queries. · Coding medical terms based on medical dictionaries for adverse events, concomitant diseases, and concomitant medication. · Performing quality control checks. · At peak times, helping with logging, entry, and filing of Case Report Forms. · Conduct other special projects as assigned.

REQUIREMENTS · Bachelor’s degree in related field and 1+ years of data management experience in a pharmaceutical or clinical research setting, or equivalent. Candidates with lesser education may qualify if experience and demonstrated skills are commensurate. · Computer related course work or on the job computer experience with a clinical data management system, Clintrial preferred. · Good oral and written communication skills and interpersonal skills.

3 positions available

Clinical Data Manager

Positions range from data coordinators to senior clinical data managers. Bachelor's Degree, with pharmaceutical experience a plus. Knowledge of structure of clinical trials databases. Database set-up, protocol review, and CRF design experience preferred. Strong communication and analytical skills required. SAS and/or Oracle experience a plus.

3 positions available

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