What are the responsibilities and job description for the Genomic Medicine Scientist II (East Coast) position at 1010 Parexel International, LLC?
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. Are you passionate about advancing genomic medicine and making a real impact on clinical trials? Join our dynamic team as a Genomic Medicine Scientist II and play a crucial role in revolutionizing patient care through cutting-edge genetic and biomarker research. What You'll Do: • Craft and negotiate pivotal genetic and biomarker language for clinical trial informed consents • Ensure ethical and compliant genetic research by documenting restrictions on clinical trial samples • Collaborate with global teams to drive innovation in genomic medicine What You Bring: • BA/BS degree with at least 5 years of relevant experience in genomic medicine or related field • Proven track record in global clinical trials and proficiency with associated systems (eTMF, LIMS, etc.) • Expertise in genetic informed consent and global negotiation • Self-motivation and ability to thrive both independently and as part of a high-performing team • Exceptional problem-solving skills and ability to manage multiple projects under tight deadlines • Strong communication skills to effectively partner with internal and external stakeholders Why Join Parexel: • Be at the forefront of genomic medicine, working on projects that directly impact patient lives • Grow your career in a supportive environment that values innovation and continuous learning • Collaborate with world-class experts in a fast-paced, cutting-edge field • Work closely with a large global pharmaceutical company as a dedicated partner on their programs from your home Candidates located in the EST are preferred, however, consideration will be given to exceptional candidates in the CST who have the ability to work East Coast hours #LI-LB1 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. Headquartered near Boston, Massachusetts and in Durham, North Carolina, Parexel has over 16,000 employees, with offices that support clients in over 100 countries around the world. We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.