Global Regulatory Manager

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for a Global Regulatory Manager (GRM) to join our A-team (hybrid*/remote). The Global Regulatory Manager is responsible for managing regulatory activities, developing and implementing strategies for timely (regulatory) approvals, ensuring timely preparation and submission of local, regional and global submissions to RAs/IECs/IRBs, ensuring the quality, content and format of regulatory submissions; serving as a direct point of contact for regulatory questions raised by the Sponsor, Allucent's Senior Leadership team, Business Development, Auditors and Inspectors. In this role your key tasks will include{{:} } • Contributes to the KOM if required to cover aspects related to RA/IEC/IRB submission and approval • Develop Regulatory and Ethics Submission Plan (RESP) • Coordinate the preparation of RA/IEC/IRB submission, including amendment submissions{{:}} will work alongside the Global Start-up Manager/PM ensuring submissions are performed according to internal and client expectation • s Plan realistic timelines for submissions and approvals at study & country leve • l Act as a source of information for Sponsors, Senior Leadership, Global Study Start-up Managers, Pharmacovigilance, Business Development, Auditors and/or Inspectors for Regulatory Requirements in countries participating in a clinical tria • l Represent the company in interactions with RA/IRB/IEC reviewers to pursue approvals, obtain information, and clarify issue • s Coordinate the Site Activation Specialists, Global Submission Specialists and Global Start-Up Assistants during preparation, compilation and submission to RA/IEC/IRB until the corresponding approvals are in plac • e Review and finalize Master SIS/ICF cycle together with Sponsor and/or CBU and distribute approved Master SIS/ICF to the countrie • s Oversee Country and/or Site-Specific (*if applicable) SIS/ICF Review/ Finalization and Approval Cycle with Sponso • r Draft and contribute as Subject Matter Expert (SME) in the field of Regulatory Oversight activities to the evaluation/improvement of processes and procedures within the Quality Management Syste m Requiremen tsTo be successful you will possess{{ : • }} Bachelor's Degree in Healthcare or Biological Science and minimum 3 years of experience in drug development and/or clinical research; or equivalent combination of education, training, and experien • ce 5-10 years of Global Regulatory Submissions experien • ce Thorough knowledge of GxP, GDPR, EU CTR and EU CTD and applicable (local) regulatory requiremen • ts Previous sponsor facing experience a significant advanta • ge Good understanding of Regulatory Submission requirements, preferably through several years of Submission experien • ce Strong written and verbal communication skills including good command of English langua • ge Strong organizational skil • ls Representative, outgoing and client focus • ed Ability to work in a fast-paced challenging environment of a growing compa • ny Proficiency with various computer applications such as Word, Excel, and PowerPoint requir ed Benef itsBenefits of working at Allucent include{ { • :}} Comprehensive benefits package per locat • ion Competitive salaries per locat • ion Departmental Study/Training Budget for furthering professional developm • ent Flexible Working hours (within reas • on) Opportunity for remote/hybrid* working depending on locat • ion Leadership and mentoring opportunit • ies Participation in our enriching Buddy Program as a new or existing emplo • yee Internal growth opportunities and career progress • ion Financially rewarding internal employee referral prog • ram Access to online soft-skills and technical training via GoodHabitz and internal platfo • rms Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on proje • cts Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employ ees Disclaimers{ {:}}*Our hybrid work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our global off ices."The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively "Allucent"). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources." #JC-1