Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Process and Procedural Document Lead - FSP
Job ID R0000034511 , MexicoManage the Clinical Medical Controlled document (CMCD) process and procedural document portal (relational database that includes business process modeling and allows for management of controlled documents and associated information with an end user interface which provides the business access to internal Pfizer colleagues, auditors, vendors, and regulatory authority inspectors), structure, content, quality and core and end user implementation from a global and local country & functional area perspective. The responsibilities include overseeing and performing quality checks for all processes and associated content and documentation for consistency and standards and assisting process documentation designer with development, revision, maintenance and oversight of specific activities, such as mapping process flows and associated content. This job also leads the development of departmental metrics and other reporting activities; facilitates/contributes to the process evaluation and integration of acquired company and/or asset related programs into Pfizer processes; contributes to compliance and audit/inspection readiness strategies and plans; and is responsible for ensuring high quality execution of controlled procedural documentation management used for the conduct of business in clinical, medical, regulatory, safety and quality assurance organizations in compliance with regulations, laws, company policy and best practices.
- Serve as the subject matter expert and liaise with Information Management partners for user acceptance testing new versions of the underlying portal management software or resolution of technical issues.
- Oversee support staff and contingent workers in daily activities related to the process portal, including training on process enhancements, and providing feedback and remediation.
- Enter and maintain data/information into the CMCD process and procedural document portal by collaborating with the CMCD authors.
- Independently manage the S&T query assistant website business process and content of over 1200 questions/answers.
- Lead special projects related to process portal as requested by supervisor.
Departmental Metrics
Independently prepare monthly/biannual/annual metrics, identify and evaluate metric trends; lead the review, endorsement, issue follow-up/resolution, and communication of metrics.
Controlled Procedural Documentation Management
QUALIFICATIONS / SKILLS
- A scientific or technical degree is preferred.
- Business degree and/or coursework with specific training in the following is preferred:
- process modeling, design, analysis and improvement methodologies and tools
- data analytics, including data connections, query design, chart/visual development and tools In general, candidates for this job would have the following levels of education/experience:
BS and over 7 years; MS and over 5 years, or 10 years relevant experience in pharmaceutical industry.
- Experience in process design and modeling methods, demonstrated ability to design effective processes.
- Demonstrated experience in project management and implementation techniques.
- Previous continuous improvement experience considered a plus.
- A strong working knowledge and understanding of drug development processes, database structures, relational database management software, and data analysis tools.
Strong interpersonal skills with a demonstrated ability to influence/interact with many levels of technical and business staff. Excellent analytical and organizational skills are required. The candidate must also possess very good communication skills (both written and verbal).
#LI-LG4
#LI-REMOTE
Recently Viewed Jobs
You have not recently viewed any jobs
View all jobs