Manager, Start-up and Regulatory Affairs

Summary

Join Ergomed PLC, a thriving CRO specializing in Oncology and Rare Disease, as their Manager, Study Start Up and Regulatory. This role demands developing regulatory strategies, completing study start-up and regulatory deliverables, and actively supporting senior management in business development. You will provide strategic guidance and mentorship to junior team members, potentially managing staff. Responsibilities include overseeing project deliverables, developing timelines, providing expert client advice, managing budgets, and ensuring regulatory compliance. The position requires a degree in a relevant field, at least 3 years of pharmaceutical/CRO experience (2+ years in a leading role), and proven global project management skills. Ergomed offers competitive salaries, career development opportunities, a supportive work environment, and a multicultural team.

Requirements

• Degree in Chemistry or Life Sciences, Nursing or equivalent experience
• Minimum 3 years within pharmaceutical or CRO industry or Regulatory body, of which at least 2 years in a leading/project management role
• Proven ability to successfully manage global projects
• Expert knowledge of ICH GCP and/or GVP and comprehensive understanding of relevant legislation/ regulatory requirements globally
• Excellent organizational and management skills are essential attributes
• Excellent planning, strategizing, managing, monitoring, scheduling, problem-solving and critiquing skills
• Exceptional written and verbal communication skills to clearly and concisely present information
• Outstanding interpersonal skills in a fast-paced, deadline oriented, and changing environment
• Remarkable attention to detail
• Excellent ability to manage multiple tasks, set priorities, and adapt to changing work assignments
• Ability to exercise sound judgment and make decisions independently
• Excellent self-motivation and motivation skills
• Proficiency in English, both written and verbal
• Good presentation, documentation and interpersonal skills. Proficient in MS Office (Word, Excel and PowerPoint), outlook and Internet

Responsibilities

• Assume leadership and functional representation for projects and/or deliverables of medium/high complexity ensuring effective and rapid coordination and management and execution of SSU/regulatory tasks, driving the team to meet the agreed targets and to comply with the agreed procedures, trackers and templates
• Develop strategy and manage set up activities (SSU RA Management Plan, procedures and core documents) ensuring compliance and consistency with department standards. Support team members in preparing project strategy, identifying issue and providing resolution
• Provide strategic input to internal and external customers and promptly identify and address any risk/potential risk by implementing preventive measures. Problem solve and ensure satisfactory resolution of performance issues or delivery failures
• Ensure preparation, collection, review of regulatory information and documents to support submissions to FDA, EMA and national authorities (CTA/INDs, MAAs/NDAs/BLAs, ODDs, PIPs) as well as Ethic Committees/IRBs for initial authorisation and maintenance, in compliance with the applicable regulations
• Provides oversight of all project SSU deliverables which encompasses all activities from site selection through site activation ready
• Develops and manages integrated site start-up timelines and reports weekly progress including plans to address potential timing risks/gaps
• Provide expert advice to Clients addressing complex SSU/regulatory queries ensuring consistent and high-quality advice across all regions
• Ensure that all communications with Regulatory Authorities and Ethics Committees/IRBs are carefully tailored to the specific requirements and tale place only when essential guidance cannot be obtained through other available resources
• Reviews the project SSU budget and scope of work with the project PM against project milestones and budget to ensure project profitability. Pro-actively discusses corrective measures with the project PM where necessary to keep project in line with budget and gross profit expectations
• Assist in securing new business or repeated business by participating to BDMs, developing and reviewing regulatory sections of proposals, regulatory costing and budgets
• Provide training, coaching and mentoring to junior members of staff
• Foster professional working relationships with internal and external contacts at the local and international levels to ensure smooth and efficient service delivery
• Ensure collection, QC review and timely dissemination of all regulatory intelligence related to departmental deliverables. Support interpretation and impact analysis on legislation
• Support client qualification activities. Ensure audit readiness and assign team members to participate as departmental representatives for audits/inspections and provide responses to any findings/follow up questions
• Contribute to the assessment and qualification of new vendors and ensure appropriate training and compliance with company standards. Support ongoing evaluation of existing vendors
• Drive department / company initiatives, act as a change champion and successfully manage implementation of the changes (communication, timing and implementation plan)

Benefits

• Training and career development opportunities internally
• Strong emphasis on personal and professional growth
• Friendly, supportive working environment
• Opportunity to work with colleagues based all over the world, with English as the company language
• Competitive salary
• Dynamic team of colleagues in a fast-growing company – possibility for your quick career growth
• Multicultural environment, English as a company language
• Strong emphasis on personal and professional growth