Sr. Scientist/Project Manager
Clinical Research Management - San Antonio, TX

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Growing and well-respected biomedical (clinical, basic and applied) research firm has openings. If you are passionate about research, and are looking for a firm that shares your passion, and provides competitive salaries with a strong benefits package, join the ClinicalRM team.

We are currently seeking a Sr. Scientist/Project Manager for the San Antonio, Texas area.

RESPONSIBILITIES:

  • Provide appropriate technical recommendations regarding best strategies and scientific approaches to achieve program objectives.

  • Attend weekly scientific reviews, provide continuous feedback and weekly reports to include laboratory testing, patient enrollment and samples analyzed to appropriate personnel following objectives and timeline thresholds.

  • Periodically accomplish technology assessment for associated molecular diagnostic technology developments.

  • Test and evaluate diagnostic platforms for various disease disorders in accordance with study design documents. Technologies will include but are not limited to Real Time Polymerase Chain Reaction (RT-PCR) and Microarray. Provide reports of test outcomes and evaluations of diagnostic platforms shall be provided to appropriate personnel within 10 working days of completion.

  • Perform DNA sequencing studies to determine biomarkers and other relevant parameters in support of approved protocols.

  • Oversees the formulation of research reports and may be required to provide additional reports from various protocols as requested (i.e., reports to higher headquarters, accrediting agencies, research partners, etc.)

  • Works with PIs to design research studies and methods to collect data in a scientifically sound manner. Reviews clinical or medical research protocols and recommend appropriate statistical analyses. Calculates samples size requirements for clinical studies. Determines project plans, timelines, or technical objectives for statistical aspects of biological research studies.

  • Provides bio-statistical consultation to PIs or colleagues.

  • Writes detailed analysis plans and descriptions of analyses and findings for research protocols or IRB approved protocols.

  • Analyzes clinical or survey data using statistical approaches including but not limited to longitudinal analysis, mixed effect modeling, logistic regression analysis and model building techniques.

  • Translates statistical and research outcome information into documents relevant to manuscripts/presentations being published by investigators. Prepares written synthesis of analysis results for inclusion in research manuscripts, presentations, and reports, as requested. Assesses the adequacy of the presentation of data, methods and purported objectives of the research projects.

  • Translates statistical and research outcome information into documents relevant to manuscripts/presentations being published by investigators. Prepares written synthesis of analysis results for inclusion in research manuscripts, presentations, and reports, as requested. Assesses the adequacy of the presentation of data, methods and purported objectives of the research projects.

  • Assists the PIs to refine the specific aim, questions, hypotheses, and/or objectives of the research protocols.

  • Designs a randomization scheme if required for the study.

  • Works with the designated statistician to clean and prepare data sets for analyses.

  • Assists in directing and overseeing institutional research.

  • As required, may have supervisory responsibility.

  • Maintain a safe workplace ensuring that he/she is aware of and observes appropriate safety and occupational health rules and regulations. Employee is required to attend safety training relative to his/her position and report any infractions of safety procedures to the facility Safety Officer.

  • Performs light duties and other related duties as required and assigned.

  • MINIMUM QUALIFICATIONS:

  • PhD in Molecular Biology or related field.

  • Minimum of 3 year of research experience.

  • Demonstrated history of publications in scientific peer reviewed journals.

  • Experienced with computer programs including Microsoft Office Products.

  • Prior experience with statistical analysis and statistical software packages.

  • Demonstrated and proven leadership ability in a laboratory environment.

  • Ability to multi-task and meet deadlines.

  • Must be able to work independently following a brief period of specific technical training.

  • Qualified candidates will receive consideration for employment without regard to race, color, religion, sex, or national origin. Candidates for positions under ClinicalRM’s contracts with the Department of Defense (DoD) will be required to pass one or more background/security investigations conducted by the DoD, U.S. Army, or other Federal Government agency. Such investigations may include criminal records and credit history checks.

    ClinicalRM is an Affirmative Action-Equal Opportunity Employer

    www.clinicalrm.com

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