Associate, Regulatory Operations

World Courier Inc.

Oakville, Manitoba, Canada

Oakville, Manitoba, Canada

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À propos

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!# **Job Details****Primary Duties and Responsibilities:*** Build and maintain a positive and productive liaison with internal and external contacts, including interfacing with potential clients.* Use various internet document transfer sites to download client files and upload files ready to be sent back to our clients.* Use, manage and maintain submission files on the company shared drive and submissions drive as per company standard.* Create and format e-compliant documents as per clients’ needs using Microsoft Word, Adobe Acrobat (and associated plug-ins), Excel, Power Point.* Create eCTD submissions using the eCTD submissions builder, validation software and electronic submissions viewer.* Create NeeS submissions, as needed, and coordinate any necessary shipments with any Coordinator or Senior Coordinator of the Regulatory Operations department.* Quality checking all submission types.* Trouble shoot and fix issues, on a document and submission level.* Send eCTD submissions via the ESG and CESG gateway.* Burn CDs/DVD’s, create appropriate labelling if required.* Create courier waybills, pack and ship submission materials ir required.* Enter time into Paymo, or company chosen database, on a daily basis.* Attend and contribute to weekly department meetings.* Maintain professional regulatory and documentary knowledge in order to provide effective consulting advice.* Assist with the creation and review of process documentation / SOP’s.* The Associate is responsible for in depth training of other department members, as needed, on a software, document and submission level.* The Associate may be asked to complete additional and other department services as required.#LI-SH1**Experience and Educational Requirements:*** B.Sc in life sciences and/or typically 5-7 years of daily working experience in Regulatory Operations**Minimum Skills, Knowledge and Ability Requirements:*** At least 5+ years of daily hands-on Regulatory Operations experience minimum* Exceptional understanding of a wide variety of submission types (Cdn and U.S.).* Excellent written and verbal communication skills.* Exceptional computer skills in advanced Microsoft Word, Adobe Acrobat, Excel and Power Point.* Advanced knowledge and skills in IT.* High knowledge of Non-eCTD electronic Submissions (NeeS).* Has a complete and thorough knowledge of all eCTD software used at Innomar.* Excellent understanding of Regulatory Operations industry guidances and a general understanding of Regulatory Affairs industry guidances.* Ability to multitask and balance several projects and ad-hoc requests at once.* Has a complete understanding of client confidentiality and the importance not to cross project information with one another.* Results oriented with proven time management, organization and prioritizing skills.* Must have an acute ability for attention to detail.* Ability to work well individually and as a team.* Has a positive attitude and works for the greater good of our clients, the team and the company.* Is responsible for company supplied hardware and software; contacting Innomar IT when needed for assistance.* Ability to manage independently and obtain individual and department goals.* Excellent project management skills – expected to see all projects through to completion.* Expected to take on, as assigned, with little to no assistance from Director of department.* Expected to coordinate with RA and Regulatory Operations team members, and keep them apprised on submission status, in order to complete all projects on time.* Independently able to identify, trouble shoot and fix any issues which arise.* Correct document placement within the eCTD structure is understood. Submissions should have virtually no errors upon first validation.* Able to identify, at all times during project, any progress on any specific task. Coordinates, on their own, any project management meetings needed and reports back to Director any needed information.* Expected to keep accurate, up-to-date records as per company/department guidelines.* Ability to consistently meet extremely tight deadlines.* Excellent conflict resolution capabilities and ability to spearhead issues (professionally) and successfully solve as they arise.# ******What Cencora offers******We provide compensation, benefits, and resources that enable a highly inclusive culture and support our team members’ ability to live with purpose every day. In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness. This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave. To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more.Full time# ********Equal Employment Opportunity********# Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law.The company’s continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory.Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call or email We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned# **Accessibility Policy***Cencora is committed to fair and accessible employment practices. When requested, Cencora will accommodate people with disabilities during the recruitment, assessment and hiring processes and during employment.*# **Affiliated Companies:**Affiliated Companies: Innomar StrategiesCencora is a leading global pharmaceutical solutions company that is committed to improving the lives of people and animals everywhere. We connect manufacturers, providers, and patients to ensure that anyone can get the therapies they need, where and when they need them.We’re a purpose-driven organization, where all of our team members around the world are united in our responsibility to create healthier futures. We work together every day to help our partners bring their innovations to patients worldwide, creating unparalleled access and impact at the center of health.2.) **Be Wary of Unrealistic Promises:** Exercise caution If a job posting offers high salaries and minimal qualifications. Legitimate jobs will have realistic expectations and provide detailed job requirements. Jobs at Cencora can be found on Cencora.com/careers
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Oakville, Manitoba, Canada

Compétences linguistiques

English

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