Ground every answer in facts on this page and the original listing. We never invent Glassdoor-style reviews or salaries that are not in our data.
Strong fit if you already run high-stakes regulatory submission programs at director scope in biopharma and want an on-site lead role in Morris County, NJ at a large product company (Gilead). Thin DATA on pay, employee sentiment, and formal cert paths—validate those offline.
As Director, Submission Project Management Lead at Gilead, the day centers on end-to-end regulatory submission programs: aligning cross-functional owners (CMC, clinical, labeling, safety), locking timelines and risk registers, driving document readiness, and steering dossier packages through internal gates toward agency filing. Expect heavy stakeholder orchestration, status discipline, and decision logs more than pure people management alone.
DATA lists no mapped cert family or paid training resources. Strength for this title usually sits in regulatory submission PM craft: CTD/eCTD awareness, RIM tooling, cross-functional timeline control, and inspection-ready documentation habits—built on the job rather than a prescribed cert path here.
No. The listing is for Parsippany-Troy Hills / Morris County, New Jersey, with remote flagged off.
Founded in 1990 and associated with gilead.com; other workplace metrics (pay bands, star ratings) are not in DATA.
No. The certs payload has an empty family and no resources, so no costs or cert names should be assumed.
Website: gilead.com
Public cache only — not an employee review.
Director, Submission Project Management Lead at Gilead Sciences, Inc. in Parsippany Troy Hills, Morris County Position Summary Gilead Sciences, Inc., a leading biopharmaceutical company dedicated to discovering and delivering innovative therapies for serious diseases, is seeking a Director, Submission Project Management Lead to join our dynamic team. This role will be based in Parsippany Troy Hills, Morris County, and offers the opportunity to contribute significantly to advancing cancer treatments. Your Responsibilities Lead project management activities for regulatory submissions, ensuring timely delivery of high-quality materials to global regulatory agencies. Coordinate cross-functional teams, including medical affairs, clinical research, and quality assurance, to ensure seamless submission processes. Develop and maintain project plans, timelines, and key performance indicators (KPIs) to track progress and meet deadlines. Identify and mitigate risks associated with regulatory submissions, ensuring compliance with all relevant regulations and guidelines. Collaborate with external partners and consultants to ensure the accuracy and completeness of submitted materials. Requirements Minimum 10 years of experience in project management within the pharmaceutical or biotech industry, with at least 5 years in a leadership role. A bachelor’s degree in life sciences, business administration, or a related field; an advanced degree is preferred. Proven track record of successfully leading complex regulatory submission projects from start to finish. Strong organizational and time management skills with the ability to prioritize multiple tasks simultaneously. Excellent communication and interpersonal skills to effectively collaborate with cross-functional teams and external partners. Working at Gilead Sciences, Inc. Gilead Sciences, Inc. is committed to fostering a collaborative and innovative work environment where every employee can contribute to our mission of curing cancer. Our culture values diversity, inclusion, and continuous learning, providing employees with the resources and support needed to thrive both professionally and personally. Applying for This Role To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there. We look forward to hearing from you!
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