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Study Director I, Biomarker, Pre-Clinical

JOB SUMMARY:
The purpose of the Study Director I position is provide hands-on experimental study design, performance, data analysis and reporting, with particular emphasis in flow related studies
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PRIMARY RESPONSIBILITIES:
  • Study design, protocol development and optimization, and study report writing and reviewing.
  • Genomics/molecular biology platform development and quality control.
  • Products registration and application, laboratory certification etc.
  • Study design, protocol development and optimization, and study report writing and reviewing.
  • In charge of internal/external project execution, management, and timely delivery of quality data.
  • Resolve scientific and other issues to reach client satisfaction. Communication with external and internal partners/clients.
  • Provide data report and information necessary to facilitate Business Development team activities.
  • Scientific and technical training of group members.
  • Laboratory/team building and daily work management.
  • SOP writing, reviewing, and implementing.
  • Complete other assignment timely from upper management.
  • Follow all health and safety standards as outlined by the QA department.

EDUCATION, KNOWLEDGE, AND EXPERIENCE REQUIREMENTS:
  • Recent Ph. D. in Molecular Biology, Immunology, Immuno-oncology or any other oncology-related life science discipline.
  • Excellent English verbal and written communication skills, excellent interpersonal skills and collaborative spirits.
  • Self-motivated, detail-oriented and goal-oriented.
  • Good at literature reading and be able to creatively resolve different challenges, can use English as working language.
  • Familiar with Biological and Office software, familiar statics analyses software.
  • Good at business to have good communication skills and team cooperation spirit.

SKILL REQUIREMENTS:
  • Broad expertise and hands on experience in nucleotide isolation, PCR, qPCR, ELISA, MSD and NGS related technology platforms will be a plus.
  • Capable of experimental design, protocol development, and data report writing.
  • Capable of trouble shooting, and critical data analysis.
  • Demonstrated capability of team building and management
  • Excellent communication skills, oral and writing.
  • Capable of scientific presentation, both oral and writing.
  • Hard working and self-motivated.
  • Efficient and capable of meeting timelines.
  • Open to new ideas, ambitious, innovative and result oriented.
  • Comfortable using computers, including an advanced knowledge of the Microsoft Office suite, e-mail, and internet.
  • Able to multi-task with a high degree of professionalism and diplomacy.
  • Willing and able to work within a Quality System with oversight by QA and other regulatory bodies.
  • Able to troubleshoot effectively and solve scientific problems with little to no supervision.
  • Able to find, read, and understand relevant scientific literature.
  • Able to work across teams by being a flexible team player.

WORKING CONDITIONS and PHYSICAL REQUIREMENTS:
  • PC2.
  • Sitting for long periods of time.
  • Standing for long periods of time.
  • Prolonged computer usage.
  • Able to lift up to 25lbs.
  • BSL-2 Lab Environment.
  • Normal office environment.