• Set up and execute laboratory experiments independently and in collaboration with team members
• Perform molecular, biochemical and cellular techniques: eg cloning, PCR, western-blotting, immunoprecipitation, ELISA, immunohistochemistry
• Maintain cell cultures
• Prepare and autoclaves media; washes glass and plastic ware
• Maintain lab supplies including reagents, chemicals, primary and secondary antibodies, plasmids and cell lines
• Present progress during group meetings

• B.Sc. in Biology or related field
• One - three years of related experience in a research environment with hands-on experience in molecular and cellular biology techniques
• Motivated, creative thinking and strong ability to troubleshoot;
• Team player and capable of working independently
• Strong organizational and oral and written communication skills

New Jersey or  San Diego location

• Collection and interpretation of all clinical data (safety, efficacy).
• Interactions with Investigators regarding conduct of the study, clinical observations and evolving strategy.
• Providing medical expertise and supporting cross-functional alignment throughout all stages of development.
• Medical monitoring of clinical trials, as well as support for the formation of risk management plans.
• Key contributor to the strategy of the clinical development plans and primary driver of clinical study reports.
• Ensuring compliance with local and global standards of Good Clinical Practice (GCP) and ensuring that regulatory requirements are met.
• Maintaining current knowledge of medical matters and diffusing this knowledge, where required.

• M.D. degree and licensed physician with training in Oncology or Hematology / Oncology.
• Three (3) or more years of clinical research experience in a biotech, pharma and/or contract research organization is required; five (5) or more years is preferred.
• Additional experience and/or training across Immunology is required; Oncology experience and/or training is desired but not required.
• Strong medical monitoring experience is critical.
• Experience in writing and conducting clinical protocols (beyond Phase 2 preferred).
• In depth understanding of the scientific method and clinical applications based on medical, scientific and practical rationale.
• Knowledge of GCP, FDA and EMEA regulations and guidelines, as well as applicable international regulatory requirements.
• Ability to effectively present ideas and document complex medical / clinical concepts in both written and oral communications; ability to influence.
• Demonstrated ability as a medical expert in a matrix environment.
• Strong leadership ability including traits of flexibility and innovation.
• History of solving problems while exhibiting superior judgment, and a balanced, realistic understanding of issues.
• Ability to multi-task, overseeing different activities and different projects simultaneously; attentive to details.
• Personal responsibility for delivery of quality output according to timelines.
• Flexibility and the ability to drive change and simplify processes.
• Team work and cross-functional alliance skills.
• Desire and ability to learn the space and to be an integral part of a growing organization; willingness to be an extremely “hands on” contributor as the Company’s medical department is established and the Company grows over the next 15-18 months.