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Jobs at Parexel

We know just how important it is to put people first. It's with that human touch that we've played a part in nearly all of the top 50 treatments on the market. And every day, we're focused on working with industry leaders to bring life-changing healthcare to patients across the globe. Whether you join our Clinical, Consulting, Biotech, Functional Service Provider (FSP), or other teams, we're doing it With Heart ™.

Associate Regulatory Project Director / Regulatory Program Lead

Job ID R0000004084 United States of America - Remote - Northeast

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

If you are passionate about innovative therapies, love leading complex regulatory filings, and live for quality, on time, and within budget project deliverables, Parexel currently has an excellent opportunity for an Associate Regulatory Project Director / Regulatory Program Lead. This is an incredible opportunity to join a tight knit team of amazingly nice and extremely experienced Regulatory Leads!

As an Associate Regulatory Project Director / Regulatory Program Lead you will provide leadership to highly experienced project teams and manage the day-to-day operations and complexities of preparing and filing NDA and/or BLA applications. You will strive to achieve operational excellence through on time delivery that is within budget and to the highest quality with the goal to exceed client expectations.

Qualifications:

Successful candidates must at minimum, possess an undergraduate degree in a clinical or health related field: advanced degree preferred, along with at least 10-15+ years' experience working in a similar capacity leading US FDA filings within a CRO, Biotech, or a Pharmaceutical Company.  Past experience overseeing a cross-functional team involved in the creation of US Regulatory Filings to include NDAs and/or BLAs is required. Previous vaccines experience is a plus!

This position also requires experience in project scheduling, managing resources and budgets and coordinating team activities, as well as experience in Regulatory Affairs related activities.

Successful candidates must also possess the following:

•The ability to build and sustain relationships
•Critical thinking and problem solving
•The ability to influence and lead teams
•Financial management skills
•Strategic thinking skills
•Attention to detail and commitment to quality
•Conflict management skills
•Consulting skills
•Contingency planning and risk management skills
•People management skills
•Excellent interpersonal, verbal and written communication skills
•Client focused approach to work
•A flexible attitude with respect to work assignments and new learning
•Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
•Bilingual candidates who are fluent in oral and written English and Korean are highly preferred
•Proficient in Microsoft Excel, Power Point, MS Project and Word.
•Experience with Parexel systems is a plus
•Willingness to work in a matrix environment and to value the importance of teamwork.
•Experience with financials and managing project budgets

Up to approximately 20% Domestic and/or International Travel may be required in the future

Employment is contingent on disclosure of your COVID-19 vaccination status and, if relevant, proof of vaccination.


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EEO Disclaimer

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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