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
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.