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PAParexel is a leading global CRO that specializes in clinical research and biopharmaceutical services to bring lifesaving treatments to patients faster.
Employee count: 5000+
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.
We are looking to fill a Principal Scientist I or II - Synthetic Chemist position working as a full-time employee of Parexel FSP on long-term remote assignment for one of our clients located in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer sponsorship.
The role is within the External Capabilities group in Small Molecule Process R&D.
Provides operational support and technical guidance for outsourced projects within Merck’s external CDMO partners to ensure the on time, high quality delivery of products and services. Some flexibility is required to work remotely with Merck’s overseas partners in another time zone during off hours (e.g., occasionally checking and responding to emails, discussions with the overseas team, in the evening as needed). This role will be mostly remote and on-site in Rahway, NJ when necessary.
Education: Degree in chemistry, or a related discipline
Principal Scientist 1: PhD or MS with 3+ years of experience, or BS with 7+ years of experience
Principal Scientist 2: PhD with 1-3 years of experience, or MS with 5+ years, or BS with 10+ years
MS with 3+ years of pharmaceutical industry experience
Strong verbal and written communication skills
At least one of the following is required:
Previous experience in project management and vendor management
Familiar with Microsoft Office suite, ChemDraw and ELN
Previous experience in project management and vendor management is a plus
Providing the operational support for chemistry sourcing projects with external partners
Providing technical guidance on sourcing projects when appropriate
Maintaining Microsoft Teams sites and SharePoint sites, and tracking project progress
Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies.
For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement.
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.
Full Time
United States +/- 0 hoursLearn more about Parexel and their company culture.
At Parexel, we speed your life-changing medicines to patients through innovative and efficient clinical research. We are proudly among the world's largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help lifesaving treatments reach patients faster. With a dedicated team of over 21,000 global professionals, we partner with biopharmaceutical leaders to design and deliver clinical trials that prioritize patient needs and experiences.
In a fast-evolving healthcare landscape, our commitment to inclusivity and diversity in clinical trial participation sets us apart. We focus on ensuring that clinical research is accessible and representative, fostering stronger relationships with communities to enhance healthcare equity. Our approach brings an empathetic focus to clinical trials, ensuring every patient’s voice is heard and valued. By adhering to our core values—Patients First, Quality, Respect, Empowerment, and Accountability—we strive for excellence in every aspect of our work, making a difference in patients' lives globally.
PA5000+ employees
1982
Peyton Howell
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