Easter Seals Jobs

JOB REQUIREMENTS: Help us change lives At Exact Sciences, we\'re helpingchange how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you\'re working to help others. Position Overview The Clinical Development Scientist II will support the development of clinical evidence plans, clinical development strategies, and study designs for clinical validation and clinical utility of LDT and in vitro-diagnostics (IVD) products. This position works with clinical development leaders and cross-functional study teams to design and execute clinical studies from concept through protocol development, data interpretation, clinical study report writing, and scientific communication (e.g., abstracts, publications, presentations). Essential Duties Include, but are not limited to, the following: Supports development of clinical evidence plans for studies related to LDT and IVD medical diagnostic products. Supports preparation of clinical study concepts and protocols. Supports data interpretation, clinical study report writing, and scientific communications, such as abstracts and manuscripts. Project management in a matrix management environment. Supports development of Clinical Development best practice and SOP documents. Supports collaborations with key opinion leaders (KOLs), biostatisticians, and outside consultants to provide clinical science inputs into clinical evidence plans. Provide support in preparation for regulatory submissions, labelling documents, and scientific meetings, such as advisory boards, consultant meetings, and investigator meetings. Support assessment of issues related to protocol conduct and subject safety. Participate in scientific meetings, advisory boards, and investigator meetings. Conduct and prepare literature reviews, as needed. Contribute to the authoring and revision of regulatory submissions. Facilitate communication of relevant scientific, clinical, or other findings to both internal and external stakeholders. Collaborate with other functions, such as clinical operations, medical affairs, regulatory affairs, research and development, and commercial/marketing, as needed. Excellent scientific writing and interpersonal communication skills. Apply strong interpersonal and communication skills,... For full info follow application link. We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, creed, disability, gender identity, national origin, protected veteran status, race, religion, sex, sexual orientation, and any other status protected by applicable local, state or federal law. Applicable portions of the Company\'s affirmative action program are available to any applicant or employee for inspection upon request. ***** APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/2DDB7A1D31AA49BE