kandydatów
Trial Master File Study Owner
Firma: Phlexglobal Poland Sp. z o.o. miejsce pracy: Lublin
Ogłoszenie numer: 6926547, from 2022-04-28
Phlexglobal is the leading technology and services organization for clinical and regulatory matters with a focus on helping clients to master their digital agenda via proven Al solutions. Phlexglobal combines software and leading expert services to offer a unique solutions portfolio with easy to achieve automation via data generation that lifts organizations to a new level of effectiveness.
As a Study Owner you will provide pivotal support and subject matter expertise (SME) at a study level, proactively ensuring our clients’ Trial Master Files (TMF) are achieving an inspection ready state.
Trial Master File Study Owner
Location: Lublin
Job description
- Document Management and Quality
- Remain familiar and up to date with relevant SOPs and processes for TMF document management.
- Able to support internal colleagues and external study team members, signposting to relevant guidance.
- TMF Management
- Support the set-up of the study-specific TMF structure, liaising with the Study Team to establish requirements.
- Monitor milestones and events to ensure TMF Completeness via eTMF functionality.
- Support development of the study-specific TMF Management Plan in collaboration with Study Team.
- Support study team through closeout and archive preparations.
- TMF Metrics
- Reviews metric report outputs with Study Teams on a recurring basis.
- Deep dive of report outputs, identifying and sharing trends and risk areas.
- Provide guidance on how to improve and maintain metrics.
- TMF Health
- Support holistic quality review and perform spot-checks for quality oversight.
- Provide TMF Health status updates to study team on a recurring basis, including verbal and/or written summaries.
- Help facilitate, track and support periodic study team TMF reviews.
- Maintain TMF Health oversight over the study lifecycle.
- Inspection Readiness
- Manage remediation and retrospective reconciliation projects.
- Manage ‘last minute’ inspection preparation activities.
- Support Audits and Inspections.
- Support implementation of CAPAs at study level.
- Identify and escalate risks and trends impacting inspection readiness.
- Develop proactive risk identification and escalation practices.
- Customer Relationships
- Facilitate TMF-focussed communication and collaboration between Sponsor and CROs.
- Communicate to the Study Manager (or equivalent) on all aspects of the TMF.
- Build proactive relationships with the study teams, providing continued SME support.
- Training & Mentoring
- Act as TMF SME, including related processes, to provide ongoing support to the Study Team.
- Support development of internal and/or external TMF-related trainings.
- Conduct training for Study Team and/or colleagues, either one to one or in a group setting.
- Mentor staff in preceding roles and be point of contact for issue escalation.
Requirements
- Communication, Collaboration, and Customer Service
- Outstanding verbal and written communication skills combined with exceptional listening skills.
- Committed team player, able to build effective working relationships with individuals at all levels of the organisation(s).
- Ability to remain calm and focussed in high-stress situations with strong skills in negotiation and conflict resolution.
- History of achievement in building strong customer relationships with demonstrated evidence of meeting customer needs and concerns through positive feedback.
- Clinical and TMF Expertise
- Minimum of 5 years relevant experience in Clinical or TMF Operations oversight.
- Thorough understanding of the processes associated with the conduct of clinical trials and document management operations.
- Experience in management of medical/clinical study records and documentation.
- Experience or knowledge of Regulatory Agency inspection expectations.
- Sound knowledge of ICH-GCP documentation requirements.
- Technical Expertise
- Experience with the following application types:
- Electronic Trial Master Files (eTMF)
- Clinical trial management systems (CTMS)
- Other clinical trial data or document management systems, as required
- MS Office (Word, Excel)
- Adept at learning and becoming proficient in new applications
- Able to impart application knowledge to support and educate team members.
We offer
- Possibility of remote work
- LUXMED private medical care and the possibility of life insurance on preferential terms
- KAFETERIA benefit platform and Multisport card
- Employee Assistance Program (psychological and mentoring support available for employees and their families)
- Opportunities to develop qualifications through the 'Litmos' training platform
- Regular development conversations
- Additional days off and attractive jubilee gratuities
- Employee Referral reward
- Flexible working arrangements
- Integration events
- Great atmosphere & international environment
Pozostałe oferty pracy w firmie Phlexglobal Poland Sp. z o.o.
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Wyświetleń: 270