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Job Details

Senior Manager Clinical Operations Neurology Remote or NJ-Based

Company name
Eisai Inc.

Location
Woodcliff Lake, NJ, United States

Employment Type
Full-Time

Industry
Manager, Operations, Pharmaceutical

Posted on
Jun 15, 2021

Valid Through
Sep 28, 2021

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Profile

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer's disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you. Job Summary The Senior Manager, Clinical Operations is responsible for the management of clinical studies in multiple Phases including, but not limited to, the development of study start-up materials, clinical supplies, case report forms, contracts and budgets, investigator meetings, and regulatory document filing. The immediate need is for the Sr. Manager, Clinical Operations to manage global studies for a major submission within the Neurology Business Group. This is an exciting opportunity for an individual with demonstrated learning agility to work on a large, high-profile global program. This position works with other team members to coordinate preparation of study protocols and final study reports. A detailed understanding of overall strategic direction, interrelationships and business needs is required. Essential Functions Managing all aspects of study progress from start-up to close-out activities and assuring adherence to intended timelines to achieve study goals while ensuring compliance with international GCP guidelines/regulations and SOPs/SWPs. Coordinating interdisciplinary activities involving study start-up: investigator meeting planning, case report form development, study drug supply design and ordering, development of contracts and budgets, data base set-up, regulatory document filing. Preparing and/or reviewing study-related documents (e.g., Study Operations Plan, Monitoring Plan, Laboratory Manual, CRF Completion Guidelines, and other study-specific documents or manuals). Preparing/reviewing site study documents (i.e., site-specific informed consent, study tools/worksheets, investigator contracts, and site payments). Collaborating with the therapeutic area team and project management to develop strategies and meet goals/timelines set forth by the team. Oversight and management of CRO to ensure successful conduct of the clinical trial by managing daily study activities to ensure data integrity and quality. Communicating with study sites, proactively recognizing problem situations and informing team members to enable issue resolution. Contributing to individual and team development through training initiatives and team building activities. Requirements Bachelor's degree in biological science, nursing, or pharmacy (or equivalent) as a minimum. Minimum 5 years of experience in the pharmaceutical industry in a position performing clinical operations functions. Experience working on large, global studies with multiple vendors involving management of submission timelines and associated processes. Demonstrated experience in the identification of emerging risks and the ability to collaboratively champion solutions within a multi-disciplinary drug development team to help resolve challenges is required. Solid project and vendor management, analytical and problem-solving skills. Prior experience with development and tracking of study budgets in excess of $20M. CNS experience preferred, but not required. Excellent written and verbal communication skills. Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans. Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information: E-Verify Participation Eisai is committed to a policy of equal employment opportunity for all employees and applicants. The Company also strives for a work environment free from discrimination and harassment. It is Eisai’s policy to comply with all applicable federal, state and local laws and regulations regarding nondiscrimination in employment and not to discriminate against any employee or applicant for employment on the basis of any protected status, including, but not limited to, race, color, national origin, religion, sex, age, disability, p regnancy, ancestry, creed, alienage or citizenship status, sexual orientation, gender identity and expression, marital status, military/veteran status, genetic information, or any other protected characteristic as established by law. Eisai is an Equal Opportunity Employer - Minority / Female / Disability / Vet

Company info

Eisai Inc.
Website : https://www.eisai.com

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