Your responsibilities

• Support publication activities by completing watch list checks and related forms, in relation to determining if external manuscript authors are included on any debarment watch lists, as per publication SOP.
• Assist with access request to the Publication application to internal and external stakeholders by ensuring that appropriate training has been completed for the requested role.
• Assist with contracting with external partners by ensuring that appropriate deliverables and clauses have been captured for the requested work and finalized.
• In partnership with the Publication Specialists and Publication Sr. Manager of Operations, verify the mng of monthly invoice processing from publication vendors (~200 invoices/month), including reconciliation of application records and confirmation of receipt of deliverables, and data capture prior to invoice payments.
• In partnership with the Publications Sr. Manager assist with data quality review and process control to ensure compliance with publications SOP.
• Metrics from each optimization activity will need to be captured in reports and dashboards so that efforts can be measured and tracked to identify future process improvements. Maintenance of job aids to ensure process controls are aligned and current.
• This role will also support the training of Pfz colleagues in best practices. This might include 'train the trainer' sessions with Pfz colleagues and vendors. Work with IMOS leadership to ensure requests are managed appropriately and timely.
• The support areas of Clinical Trial Data request include but not limited to:
• Provide end-to-end Operational Management of the clinical trial data sharing requests from submission to data package upload.
• Perform due diligence and collaborate with internal and external partners to ensure the timely review of all requests.
• Coordinate data packages for upload to Pfz supported platforms.
• Develop reports and metrics scorecard for CTDS program and ensure the accuracy and timely distribution of all reports to CTDS stakeholders.
• Manage requests in the CTDS tracking system (SharePoint, Teams)
• Ensure all requests are thoroughly reviewed and correctly documented to maintain the highest standards of quality and efficiency. Ensure tracking log is always complete and accurate.

Our requirements

• Applicants must have a bachelor's degree with 4+ years of experience OR a master's degree with 2+ years of experience OR an associate degree with 8+ years of experience with preference for a focus in science, healthcare, or related field.
• Excellent writing skills and ability to edit, summarize and interpret complicated content effectively and concisely for better understanding.
• High fluency in written English and strong functional fluency in spoken English.
• Strong organizational skills, attention to detail, and ability to prioritize multiple projects and meet deadlines.
• Ability to take initiative and work independently.
• Software: Microsoft Word, PowerPoint, Excel, Teams and Outlook.
• Demonstrated effectiveness working in a multidisciplinary, matrix team situation, and demonstrated ability to manage change and diversity.
• Developed customer service skills and teamwork spirit.
• 1-2 years' experience in pharma, pharma internship, or closely related is a plus.

What we offer

• Competitive salary rate and social package

• Wide opportunities for professional development