Eikon Therapeutics is seeking a seasoned physician to join their Clinical Development team to advance their Oncology pipeline by providing medical expertise, strategic leadership, and operational oversight for multiple clinical development studies.
Requirements
- MD or DO degree with significant experience in Oncology.
- Minimum of 5-7 years of clinical experience, including 3+ years in drug development.
- Significant experience in clinical practice with direct patient care (preferably in Oncology)
- Proven track record in leading clinical trials, including medical monitoring of early and late clinical trials and managing complex projects.
- In-depth knowledge of clinical research methodologies, GCP, and regulatory requirements.
- Ability to work effectively in a matrixed environment.
- Experience with IND and/or NDA filings is preferred.
Responsibilities
- Design and conduct early-stage or late-stage clinical development trials, including, but not limited to: assessing clinical safety and efficacy data, performing medical monitoring, and be responsible for other study-related clinical activities.
- Work closely with biomarker, discovery, and translational research scientists.
- Interpret reports, prepare oral and written results of product research, and participate in the discussion of strategies formulated within the disease areas that Eikon is focusing on.
- Collaborate closely with Clinical Science and other relevant functions within Eikon and potential partners including discovery, translational, and biomarker research scientists, toxicologists, clinical pharmacologists, drug safety specialists, regulatory representatives, as well as personnel from Global Clinical Operations, and other support functions.
- Establish strong working relationships and collaborations with external study investigators, key opinion leaders in drug development, and external alliance partners.
- Work closely with functional partners (Data Management, Clinical Operations, Biostatistics, Regulatory) to ensure an integrated and strategic approach to flawless execution and systematic oversight of study protocol(s) in clinical development in close collaboration with key functional stakeholders.
- Work in partnership with colleague study responsible physicians and clinical scientists to ensure development of high-quality study protocols including use of consistent processes/standards across studies.
Other
- Minimum of 3 day a week of onsite presence (or more as business needs require) in either of our California or New Jersey offices
- Strong analytical, organizational, and problem-solving skills.
- Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external partners.
- Passion for innovation and improving patient outcomes.
- Ability to work effectively in a team environment
