Senior Director, Good Clinical Practice & Good Pharmacovigilance Practice Quality Assurance
SOUTH SAN FRANCISCO, CAPosted 30+ days ago
Job summary
Job post source
This job is directly from IDEAYA Biosciences
Job overview
The Senior Director of Good Clinical Practice & Good Pharmacovigilance Practice Quality Assurance is a senior leadership role responsible for overseeing quality assurance activities related to clinical trials, ensuring compliance with regulatory requirements and driving continuous improvement initiatives.
Responsibilities and impact
The candidate will develop and implement GCP QA strategies, oversee compliance with GCP regulations, manage audits, and lead a team of QA professionals to ensure high standards of quality and patient safety in clinical research activities.
Compensation and benefits
The salary range for this position is $228,098 - $281,768 per year, along with a competitive total rewards package including performance bonuses, company equity, and generous health benefits.
Experience and skills
Candidates should have an advanced degree in life sciences and a minimum of 15 years of experience in the pharmaceutical or biotechnology industry, with at least 10 years in GCP QA leadership roles, and strong knowledge of global GCP regulations.
Career development
The role offers opportunities for professional growth through leadership of a high-performing team and involvement in strategic quality assurance initiatives.
Work environment and culture
IDEAYA Biosciences fosters a collaborative and inclusive environment, emphasizing teamwork and a passion for advancing oncology medicine.
Company information
IDEAYA Biosciences is a public, clinical-stage precision medicine oncology company focused on developing targeted therapeutics for patients with high unmet clinical needs, with established collaborations with major pharmaceutical companies.
Team overview
The candidate will lead a team of QA professionals, fostering a culture of quality and collaboration within the team and across the organization.
Job location and travel
This position is based in South San Francisco and requires onsite work four days a week.
Application process
Candidates are encouraged to apply through the company's Human Resources department, as all open positions and candidate activity are managed strictly through HR.
Unique job features
This role is distinguished by its strategic leadership responsibilities and the opportunity to influence quality assurance practices across clinical studies.
Company overview
IDEAYA Biosciences is a precision medicine oncology company focused on the discovery and development of targeted therapeutics for cancer. They generate revenue through partnerships, licensing agreements, and the commercialization of their drug candidates. Founded in 2015, IDEAYA has made significant strides in synthetic lethality and immuno-oncology, with a robust pipeline of clinical and preclinical programs aimed at addressing unmet medical needs in oncology.
How to land this job
Tailor your resume to emphasize your extensive experience in Good Clinical Practice (GCP) and Good Pharmacovigilance Practice (GVP) quality assurance, showcasing your leadership skills and ability to manage QA teams effectively.
Highlight your proven track record in overseeing compliance with global regulatory requirements and your experience hosting regulatory inspections, as these are critical for the Senior Director role at IDEAYA.
Apply through multiple channels, including IDEAYA's corporate site and LinkedIn, to maximize your visibility and chances of landing the position.
Connect with professionals in the quality assurance division at IDEAYA on LinkedIn to inquire about the role and gain insights into the company's culture and expectations. Potential ice breakers could include asking about their experience with specific GCP initiatives or expressing interest in their recent collaborations with major pharmaceutical companies.
Optimize your resume for ATS systems by incorporating key phrases from the job description such as 'GCP QA strategy,' 'clinical trial compliance,' and 'continuous improvement initiatives' to ensure your application passes initial screenings.
Utilizing Jennie Johnson's Power Apply feature can simplify your application process, allowing you to focus on networking and preparing for interviews while ensuring your resume is tailored and optimized for the role at IDEAYA.
Jennie Johnson works for you!
Here’s what we do to make sure you’re successful:
Targeted Resume Revamp:
We expertly craft your resume to navigate Applicant Tracking Systems (ATS) and showcase your qualifications, making you stand out as a top-tier candidate.
Job Description Dissection:
Unpack the job posting with expert analysis, ensuring your application hits every key requirement.
Bespoke Cover Letter:
Capture the attention of hiring managers with a personalized cover letter that highlights how your skills align perfectly with the job's needs.
Interview Mastery:
Prepare for interviews like a pro with likely questions, strategic answers, and insightful questions for you to ask, setting you apart as an informed candidate.
Direct Application Insights:
Receive tailored advice on the best places to apply, ensuring your applications are seen by the right employers.
Skills and Gaps Assessment:
Identify and close critical skills gaps to position yourself as the best-fit candidate for your ideal job.
Personalized Email Pitch:
Make a memorable first impression with an email template crafted to engage potential employers and initiate meaningful conversations.
In-depth Research Guide:
Leverage comprehensive research tools to gather effective insights on companies, industry trends, and role-specific challenges.
Detailed Company Analysis:
Gain in-depth understanding of your prospective employer, giving you the edge in applications and interviews.
Strategic Candidate Overview:
Understand your unique value and why companies would want to interview you, highlighting your background and positioning.