IDEAYA Biosciences (NASDAQ: IDYA) is a public clinicalstage precision medicine oncology company committed to the discovery development and commercialization of targeted therapeutics for patient populations with high unmet clinical needs. Our approach integrates extensive capabilities in identifying and validating translational biomarkers with small molecule drug discovery to select patient populations most likely to benefit from the therapies we are developing. We have developed an industry leading platform and pipeline in precision medicine by applying these capabilities across multiple approaches such as direct targeting of oncogenic pathways and synthetic lethality which represents an emerging class of precision medicine targets. We believe this diversified approach will enable us to deliver the right medicine to the right patient to drive a more robust clinical response. IDEAYA has established strategic collaborations with GSK Merck Pfizer and Gilead but whollyowns or controls its four mostadvanced clinical programs and we are committed to building a bestinindustry organization to deliver our precision medicines to the people who need them.
When youre at IDEAYA you will be in the midst of brilliant minds working on precision medicine therapies to help cancer patients. We are passionate and committed about being on the forefront of oncology medicine which means we all have a high internal drive that is at the very core of every person at IDEAYA. We are inquisitive ask deep questions and are datadriven innovators who like to collaborate and use teamwork to move science forward. For more information please see www.ideayabio.
Notice to Agencies and Recruiters: All open positions and candidate activity are strictly managed through Human Resources. Please note that our policy is that recruiters do not contact employees/hiring managers directly to solicit business and/or present candidates. Submission of unsolicited resumes prior to an agreement set in place between the Human Resources Department and the recruiting agency will not create any implied obligation. Please note that failure to comply with this request will be a factor in developing a professional relationship with IDEAYA Bio. Inquiries regarding developing a recruiting relationship with us may be directed to
Position Summary:
The Medical Director is responsible for providing medical direction management and review of clinical trials and product development. Specific tasks may include design of clinical development program plans as well as clinical protocol development medical monitoring of clinical trials and analysis of study data and preparation of trial reports and related regulatory documents. The individual may also serve as a Development Project Leader for a specific asset and will interact with most functions to ensure the successful progress of projects and clinical trials. This individual will have a solid understanding of all phases of clinical drug development with particular expertise in first in human clinical trials translational science and operational excellence. Excellent written and effective verbal communication skills ability to influence across functions and levels and flexibility/adaptability to work in a fastpaced environment are essential.
This position is based in our South San Francisco headquarter or San Diego office and required to be onsite four days per week per our company policy.
What youll do:
Applies disease knowledge to clinical research trial development
Drives protocol development for clinical studies in collaboration with Clinical Operations and other clinical subteam functions
Drives preparation of clinical development plans in partnership with crossfunctional team
Works collaboratively with Regulatory Affairs; drafts clinical scientific documents such as IND IND amendments Investigator Brochures Annual Reports (DSUR) and other FDA/HA submissions
Contributes to CSR preparation and finalization
Contributes to development of CRFs and data review plans
Monitors and reviews safety and efficacy data in ongoing studies
Serves as primary clinical point of contact (eligibility questions AE management) for clinical trial sites
Develops clinical abstracts and/or presents data at scientific meetings SIVs and conducts protocol training
Develops and participates in advisory boards
Keeps abreast of hematology/oncology treatments drug mechanism of action approaches to drug development and regulatory requirements
Acts as a clinical representative in variety of crossfunctional teams including early stage Research teams
Serves as clinical partner to Business Development
Requirements:
Medical degree required; hematology/oncology training and/or practice experience
Experience in industry in early phase development preferred
Thorough understanding of oncology clinical trial design including firstinhuman Phase 1 studies as well as mid and latestage trials
Experience and understanding of clinical trial data monitoring and all aspects of drug development
Knowledge of GCP and ICH guidelines
A proven selfstarter and team player with strong interpersonal skills who establishes & nurtures highly effective relationships with colleagues and key stakeholders to support and advance project goals and objectives
Critical thinker with a solutionsoriented mindset
Selfmotivated to work effectively in a dynamic environment
Possess strong organizational skills and conflict resolution abilities
$242893 $300045 a year
At IDEAYA Biosciences we care about our employees and strive to provide a marketcompetitive total rewards package including base pay an annual performance bonus company equity and generous health and wellbeing benefits. The expected salary range for this role that is based in our South San Francisco or San Diego office in California is $242893 $300045.
The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the office location where this open position is located the final candidates experience within their profession experience in the disease areas we are striving to make an impact in as a company length of time within the industry educational background and performance during the interview process.
The Company complies with all laws respecting equal employment opportunities and does not discriminate against applicants with regard to any protected characteristic as defined by federal state and local law. This position requires you to work onsite at the Companys facilities with partial workfromhome flexibility and the Company requires that all employees working in its facilities be fully vaccinated (except as required by applicable law). Therefore this position requires you to be fully vaccinated from COVID19 subject to reasonable accommodations for medical or religious reasons and/or as otherwise required by applicable law. The Company considers you fully vaccinated once 14 days have passed since you received either the second dose in a twodose COVID19 vaccine series or a singledose COVID19 vaccine. The vaccine must have been FDA approved have emergency use authorization from the FDA or for persons fully vaccinated outside of the U.S. be listed for emergency use by the World Health Organization.
Total Rewards:
Along with our inspiring mission and highly collaborative and inclusive environment IDEAYA offers a competitive total rewards package that reflects our payforperformance philosophy where employees are eligible to be considered for meritbased salary increases company discretionary shortterm incentive plan participation and company discretionary stock option awards (based on board approval). Our comprehensive benefits package includes but is not limited to medical/dental/vision coverage 100 company paid for employees and 90 company paid for dependents) 401k ESPP and wellness programs.
IDEAYA is an equal opportunity employer. In accordance with applicable law IDEAYA does not discriminate in hiring or otherwise in employment based on race color religion sex national origin age marital or veteran status disability sexual orientation or any other legally protected status. EOE/AA/Vets.
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