ppWorldwide Clinical Trials is a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. /p pWe are a worldwide team of over 3,500 experts, bright thinkers, dreamers and doers and together we are changing the way the world experiences CROs – in the best possible way. /p pOur mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. /p h3What the Director, Regulatory Pre-Award Strategy Does at Worldwide /h3 pAccountable for senior-level leadership in establishing the operational strategy and achieving high performance and growth objectives for general regulatory affairs. Reports to Senior Vice President, Site Activation and Regulatory Affairs. This role has project-specific dotted line reporting to the Site Activation Therapeutic Leads. /p h3What You Will Do /h3 ul liOversees the delivery and performance of regulatory affairs activities and supporting roles such as Regulatory Affairs Managers and Regulatory Affairs Specialists. /li liProvides expert regulatory advice and contributes to regulatory project work for internal and external customers. /li liProvides and drives the overall planning and oversight for regulatory affairs activities including high quality and timely delivery for internal and external stakeholders and projects. /li liResponsible for regulatory affairs-related in business development activities by attending key Proposal Strategy Meetings (e.g., Executive and Strategic level), contributing to proposals and bid defense meetings by preparing regulatory sections of proposals and feasibility reports, regulatory costing and budgets, contracting process, essential document activities and other country and/or project-specific activities for regulatory affairs in support of the overall site activation strategy. /li liStays currently informed as a subject matter expert of changing regulatory affairs requirements and ensures the regulatory affairs group is proactively trained as current subject matter experts in their local area and/or other relevant areas of expertise for their role. /li liRemains current and knowledgeable with SOPs,



ICH GCP and regulatory and quality regulations as applicable and is accountable for the compliance with SOPs, ICH GCP and regulatory and quality regulations of the regulatory affairs group. /li liFosters professional working relationships with internal and external contacts at the local and international levels to ensure expeditious submission/approval of regulatory dossiers. /li liResponsible for the preparation of technical /master study documentation in accordance to the study requirements, contracted scope and specific legislations. /li liAccountable for the performance and development of Regulatory Affairs Managers and Regulatory Specialists to ensure critical path activities are completed on time and ensures optimal start and conduction of regulatory affairs activities to meet project deliverables. /li liEnsures high quality performance of deliverables are applied within the projects assigned to line reports and promptly identify and address any risk/potential risk by implementing preventive measures and mitigation plans. /li liProvides expert regulatory knowledge with the Site Activation functional leads and the rest of project team to establish risk mitigation strategies/contingency plans and present these to sponsors. /li liManages regulatory affairs team workload and provides input for allocations etc. according to demand (including holidays approval and proper back-up). /li liBuilds, develops, coaches and leads a team of direct reports responsible for regulatory affairs activities globally. /li liMay attend customer facing meetings related including Governance, bid defense, and escalation. /li liParticipates in the development and maintenance of departmental processes, tools, policies, SOPs and associated documents. /li liAssists the Site Activation leadership team and/or other company departments in leading or participating in department initiatives, tasks forces, and additional training where necessary.



/li /ul h3What You Will Bring To The Role /h3 ul liStrong oral and written communication skills to clearly and concisely interpret and present information. /li liStrong and proven leadership and organizational management skills in planning, strategizing, managing, monitoring, scheduling, and critiquing. /li liProficiency in MS-Office applications including Microsoft Word, Excel, and PowerPoint, regulatory portals and Worldwide applications. /li liExpert understanding of clinical research principles and processes. /li liDemonstrated ability to independently manage multiple tasks in a fast-paced and changing environment while delivering in an organized, methodical and self-motivated manner to solve complex and time sensitive problems. /li liExcellent interpersonal skills in a fast-paced, deadline oriented, and changing environment. /li /ul h3Your Experience /h3 ul liA minimum four-year college curriculum with a major concentration in medical, biological, physical, health, pharmacy or other related science, OR… /li liTwo-year college curriculum or equivalent education / training (nursing degree or equivalent life science degree) and eight years’ experience within clinical research (e.g. CRA, Reg Affairs.). /li liMinimum 10 years within pharmaceutical/CRO industry, with demonstrated senior level regulatory or clinical start-up experience. /li liProficient in cross-cultural communication and proficient in both spoken and written English. /li /ul pWorldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law. /p /p #J-18808-Ljbffr

📌 Director, Regulatory Pre-Award Strategy - Europe- Remote (Barcelona)
🏢 Worldwide Clinical Trials
📍 Barcelona