Posting closing date: February 22, 2023
Date de fin d\xe2\x80\x99affichage : le 22 f\xc3\xa9vrier 2023
Status : Regular, Full-Time
Statut : R\xc3\xa9gulier, temps plein
Role Summary
As part of an agile team, will lead the ideation, strategy and development of information management solutions for the Regulatory domain; use business analysis skills and domain knowledge to elicit requirements and drive timely decisions to achieve desired business outcomes, and work across Global Regulatory, other Regulatory partner lines (e.g. Safety, Manufacturing, Pharmaceutical Sciences and Digital) to execute projects that deliver robust solutions for regulatory affairs.
ROLE RESPONSIBILITIES
Work closely with functional lines to articulate business needs for new solutions or changes to existing solutions and document business requirements for assigned solutions. Run workshops and conduct interviews with functional line SMEs to understand the business need and then ensure full and complete requirements set. Ensure endorsement from functional lines.
Document options and proposals for solution governance on how best to meet customer needs.
Drive impact assessments of business requirements and technical changes, which include the identification of processes and applications, required changes to these processes and applications, and alternatives to mitigate impact.
Coordinate user testing and acceptance of information solutions prior to deployment.
Lead continuous improvement projects to simplify and improve system use and system management.
Lead medium to large projects, following established methodologies.
Collaborate with functional lines to ensure a consistent approach with business process-specific training.
Drive active decision making through pre-existing governance with a complex set of stakeholders.
Provide direction to junior level team members supporting owned project work and work activities.
BASIC QUALIFICATIONS
Minimum of 5 years pharmaceutical industry experience in (or supporting) any of the following disciplines: clinical drug development, clinical trial management, safety surveillance and reporting, clinical project management, R&D or regulatory reporting and analytics, or regulatory affairs. Related experience in other industries will be considered.
Demonstrated strong analytical skills with ability to investigate and solve unusual and complex problems independently.
Demonstrated strong customer relationship skills and capabilities to influence and collaborate with teams.
Proven ability to communicate complex information and analyses to a variety of audiences in both verbal and written format, capable of effectively summarizing abstract concepts into clear, concise, and insightful business cases.
Proven ability to operate in a fast-paced, high-energy environment and comfort with operating in situations with significant ambiguity.
Minimum of a bachelor\xe2\x80\x99s degree (BS or BA) with higher academic qualification/degree preferred or equivalent relevant professional experience
PREFERRED QUALIFICATIONS
MS in Computer Science, Life Sciences, Business, Engineering, Statistics, or a related discipline.
Experience in building/managing solutions in one or more areas of Regulatory Intelligence and Policy, Chemistry and Manufacturing Controls, Submissions Management, Publishing, and Labeling.
TECHNICAL SKILL REQUIREMENTS
Experience with regulated systems used in pharmaceutical industry or other GxP area.
Demonstrated knowledge of application system management and change control processes, application validation and implementation in a GxP environment.
Knowledge of healthcare and/or pharmaceutical metadata and standards.
REQUIRED APTITUDES
Action oriented and energetic.
Resourceful and creative; avid learner.
Easily makes connections - Quick to establish trust and respect.
Pre-employment requirement :
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