Job added in hotlist
Applied job
Contract job
90-day-old-job
part-time-job
Recruiter job
Employer job
Expanded search
Apply online not available
View more jobs in Woodcliff Lake, NJ
View more jobs in New Jersey

Job Details

Senior Associate Regulatory Systems Support

Location
Woodcliff Lake, NJ, United States

Date Last Verified
Jul 16, 2021

Posted on
Jul 15, 2021

Apply for this job






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 Sr Associate in Global Regulatory Systems & Process Management (GRSPM) will provide support, strategies and business solutions for the development and maintenance of regulatory systems. Establishing, managing and supporting regulatory systems according to system requirements. The development of regulatory requirements and business and system support processes. Ensuring the integrity of the data either managed within the system or migrated from legacy systems. Use of QC processes and training end users for key tasks within the managed systems. Main Duties/Responsibilities - Will include but will not be limited to the following activities: Maintain the data integrity of data within the regulatory systems Ensure that Regulatory Information Systems are supported and managed according to business need and regulatory compliance Capture and implement system enhancements to optimize their operational capabilities according to business need Develop user requirements specifications for future information systems and create business justification for new systems Initiate UAT Scripts, deployment of software, design and deliver training for systems accordingly Stay current with industry best practice and software regarding Regulatory Information Management, identifies opportunities to shorten approval timelines through enhanced knowledge sharing Engage with vendors and internal partners to drive future state of-the shelf software packages. Ensure completeness of content contained in information management systems specifically as it relates to compliance Requirements BS/BA with minimum 3 years of experience with Document Management Systems. Experience in Regulatory Information Management systems supporting regulatory information or publishing tool is required. Degree in computer science or relevant field preferred Previous experience in pharmaceutical industry an advantage Experience of mapping User Requirements to Functional Specifications especially in respect of process management an advantage Skills and Aptitude Required: Strong verbal, written and interpersonal communication skills, especially relationship management, with ability to give/receive feedback and build consensus Experience in handling multiple tasks Knowledge of MS Office (Word, Excel, PowerPoint, Project), Adobe acrobat as well as being familiar with the use of multiple regulatory system applications 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. **MEMBERS ONLY**SIGN UP NOW***. 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

Sign Up Now - PharmaceuticalCrossing.com

Similar Jobs:
SUMMARY/POSITION OBJECTIVEThe Temp – Sr. Clinical Documentation Associate - Study Start-up (CDA-SSU), will serve as the primary contact for the requirements, coordination and review of essential documents required for release of I...
3542- Scientist II Microbiologist
Location : Hackensack, NJ
Fraud Notice Parexel.com Own the challenges that lead to innovation and growth 2020 Promoted to Head of Biotech Operations for Americas East, helping clients develop novel therapies with a focus on patient needs. 2019 Advanced to ...
Director, Oncology Medical Science Liaison
Location : Woodcliff Lake, NJ
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 breaki...
What I liked about the service is that it had such a comprehensive collection of jobs! I was using a number of sites previously and this took up so much time, but in joining EmploymentCrossing, I was able to stop going from site to site and was able to find everything I needed on EmploymentCrossing.
John Elstner - Baltimore, MD
  • All we do is research jobs.
  • Our team of researchers, programmers, and analysts find you jobs from over 1,000 career pages and other sources
  • Our members get more interviews and jobs than people who use "public job boards"
Shoot for the moon. Even if you miss it, you will land among the stars.
PharmaceuticalCrossing - #1 Job Aggregation and Private Job-Opening Research Service — The Most Quality Jobs Anywhere
PharmaceuticalCrossing is the first job consolidation service in the employment industry to seek to include every job that exists in the world.
Copyright © 2021 PharmaceuticalCrossing - All rights reserved. 168 192