Senior Regulatory Specialist, CTA/IND

2 tygodni temu


Warszawa, Mazovia, Polska 9605 GSK Services Sp z o.o. Pełny etat

We are now looking for a SENIOR REGULATORY SPECIALIST ( CTA/ IND) to join our Polish Hub.

Key Responsibilities:

Coordination, development, refinement of the CTA/IND lifecycle strategy, timely content & delivery appropriate to each individual regulatory agency while maintaining compliance with GSK policy and procedures. Accountable to the functional CTA/IND Team Lead for overall work plans and accountable to individual GRLs/TGs for study submission planning & delivery status. Accountability for agreed tasks and projects. Ensure independent communication, with a range of internal GSK staff, in support achievement of the assigned goals. Ensure quality of both own and submission team's work, delivering to agreed timeframes, including compliance with GSK systems and record keeping. Provide input to internal processes and written standards. To work flexibly to meet constant shifting priorities and timelines. May provide support to other activities within the CTA/IND and/or Content Delivery Team.

Why You?

What skills and expertise you will bring to the role:

Min. Bachelor's degree in biological or healthcare science (Chemistry, pharmacy, other related science or regulatory affairs). Relevant experience within Regulatory Affairs in the R&D, pharmaceutical industry or clinical trials. Broad understanding of the pharmaceutical industry, drug development environment, and R&D processes and objectives. A good understanding of Clinical Trial Directive, DIA Trial Master File Reference Model and CTA/IND submission requirements for multiple countries/submission types. Well-developed interpersonal and communication skills to work in a matrix environment effectively and build good working relationships in cross-functional teams. Written and verbal communication skills in English and Polish, ability to present information in a clear and concise manner. Ability to lead in a matrix environment and ensure delivery of objectives across cross-functional teams. Excellent organizational skills, attention to detail and commitment to deliver high quality output, even under pressures sometimes demanded by regulatory deadlines. Ability to work in multiple IT systems (filing, tracking & repositories). Mentoring experience would be an advantage. Veeva Vault experience would be an advantage.

At GSK we offer a wide range of additional benefits:

Career at one of the leading global healthcare companies. Contract of employment. Hybrid work ( 2/3 days per week from the office) Attractive reward package (annual bonus & awards for outstanding performance, recognition awards for additional achievements and engagement, holiday benefit). Life insurance and pension plan. Private medical package with additional preventive healthcare services for employees and their eligible. Sports cards (Multisport). Possibilities of development within the role and company's structure. Personalized learning approach (internal trainings, mentoring, access to online training' platforms: Keep Growing Campus, LinkedIn Learning, Business Skills, Harvard Manage Mentor, Skillsoft and external training). Extensive support of work life balance (flexible working solutions, short Fridays option, health & well-being activities). Supportive community and integration events. Modern office with creative rooms, fresh fruits every day.

#LI-GSK

#LI-HYBRID

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

GSK is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK.



  • Warszawa, Mazovia, Polska IQVIA Pełny etat

    Senior Site Activation Coordinator (Contract Specialist) Country Site Activation Join us on our exciting journey IQVIA's Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication. We are leaders in innovation and first...


  • Warszawa, Mazovia, Polska ManpowerGroup Sp. z o.o. Pełny etat

    Regulatory Clinical Trial Application Submission ManagerRegulatory Clinical Trial Application Submission ManagerDuties: Manages regulatory Clinical Trial Applications (CTA) submission activities for assigned clinical trials (Phase 1 – Phase 4 spanning the therapeutic areas Oncology, Neuroscience, Cardiovascular and Metabolism, Immunology, and Infectious...


  • Warszawa, Mazovia, Polska ManpowerGroup Sp. z o.o. Pełny etat

    Regulatory Clinical Trial Application Submission Manager Zabki, Masovian Voivodeship Duties:Managesregulatory Clinical Trial Applications (CTA) submission activities for assigned clinical trials (Phase 1 – Phase 4 spanning the therapeutic areas Oncology, Neuroscience, Cardiovascular and Metabolism, Immunology, and Infectious Disease)Ensures that the...


  • Warszawa, Mazovia, Polska ManpowerGroup Sp. z o.o. Pełny etat

    Duties:Managesregulatory Clinical Trial Applications (CTA) submission activities for assigned clinical trials (Phase 1 – Phase 4 spanning the therapeutic areas Oncology, Neuroscience, Cardiovascular and Metabolism, Immunology, and Infectious Disease)Ensures that the required regulatory intelligence is in place to comply with country-specific requirements...


  • Warszawa, Mazovia, Polska ManpowerGroup Sp. z o.o. Pełny etat

    Manpower (Agencja zatrudnienia nr 412) to globalna firma o ponad 70-letnim doświadczeniu, działająca w 82 krajach. Na polskim rynku jesteśmy od 2001 roku i obecnie posiadamy prawie 35 oddziałów w całym kraju. Naszym celem jest otwieranie przed kandydatami nowych możliwości, pomoc w znalezieniu pracy odpowiadającej ich kwalifikacjom i...


  • Warszawa, Mazovia, Polska ManpowerGroup Sp. z o.o. Pełny etat

    Manpower (Agencja zatrudnienia nr 412) to globalna firma o ponad 70-letnim doświadczeniu, działająca w 82 krajach. Na polskim rynku jesteśmy od 2001 roku i obecnie posiadamy prawie 35 oddziałów w całym kraju. Naszym celem jest otwieranie przed kandydatami nowych możliwości, pomoc w znalezieniu pracy odpowiadającej ich kwalifikacjom i...


  • Warszawa, Mazovia, Polska IQVIA Argentina Pełny etat

    Senior Site Activation Coordinator (Contract Negotiator)Country Site ActivationJoin us on our exciting journeyIQVIA's Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication. We are leaders in innovation and first to new...


  • Warszawa, Mazovia, Polska HAYS POLAND Sp. z o.o. Pełny etat

    Regulatory Affairs Specialist / Associate Manager Warszawa, mazowieckie Regulatory Affairs Specialist / Associate Manager Warszawa Warszawa, Mazowieckie, Polska Regulatory Affairs Specialist / Associate Manager Warszawa Warszawa, Mazowieckie, Polska For our client, a global FMCG company, we are looking for a Regulatory Affairs Specialist / Associate...

  • Regulatory Scientist

    2 tygodni temu


    Warszawa, Mazovia, Polska ManpowerGroup Sp. z o.o. Pełny etat

    Manpower (Agencja zatrudnienia nr 412) to globalna firma o ponad 70-letnim doświadczeniu, działająca w 82 krajach. Na polskim rynku jesteśmy od 2001 roku i obecnie posiadamy prawie 35 oddziałów w całym kraju. Naszym celem jest otwieranie przed kandydatami nowych możliwości, pomoc w znalezieniu pracy odpowiadającej ich kwalifikacjom i...


  • Warszawa, Mazovia, Polska HAYS POLAND Sp. z o.o. Pełny etat

    Senior Regulatory Affairs Specialist/Manager Warsaw, Masovian Voivodeship Job Responsibilities: 1. Stay up-to-date with evolving regulatory requirements in Europe, particularly for medical devices. 2. Offer expert regulatory advice for strategic decision-making, ensuring effective execution of regulatory strategies. 3. Manage maintenance activities and...


  • Warszawa, Mazovia, Polska GlaxoSmithKline Pełny etat

    Site Name: Warsaw, Poznan GrunwaldzkaPosted Date: May The Senior Regulatory Specialist, Country Labelling is responsible for effective coordination, communication and maintenance of regional/country labelling documents (for multiple markets/regions) and data in regulatory systems in accordance with defined standards and processes. You will provide support to...


  • Warszawa, Mazovia, Polska 9605 GSK Services Sp z o.o. Pełny etat

    What we are doing? Global Regulatory Centres (GRC) in GSK are regulatory affairs functions which bring together the operation and execution aspects for key regulatory deliverables such as new chemical entity and product expansion dossiers, labelling outputs, licence maintenance and lifecycle management dossiers, and regulatory information management....


  • Warszawa, Mazovia, Polska Smith & Nephew Pełny etat

    Regulatory Affairs Specialist page is loaded Regulatory Affairs Specialist Apply locations POL - Warsaw time type Full time posted on Posted 6 Days Ago job requisition id R74567 Life Unlimited.At Smith+Nephew we design and manufacture technology that takes the limits off living. The Regulatory Affairs Specialist is responsible for representing and...

  • Regulatory Specialist

    2 tygodni temu


    Warszawa, Mazovia, Polska GlaxoSmithKline Pełny etat

    Site Name: Poznan Grunwaldzka, WarsawPosted Date: Jun 7 2024Regulatory Specialist supports operational activities related to maintenance of marketing authorisations (MAs) across assigned markets and/or submission types in European Partnership Markets, working in close collaboration with country leads, as well as global regulatory teams/centers and local 3rd...


  • Warszawa, Mazovia, Polska Hobson Prior Pełny etat

    Hobson Prior is seeking a Senior Manager for Regulatory Operations. This role will be the primary contact for Regulatory Affairs in business projects that involve or impact data, systems, and processes. The successful candidate will ensure data compliance, accuracy, and usability, and will also provide support and training for the relevant community. This...


  • Warszawa, Mazovia, Polska Publicis Le Pont Pełny etat

    Job DescriptionAs a Regulatory Submission Specialist, in this role, you will be tasked with delving into medical documents, pinpointing the correct references for pharmaceutical marketing materials, uploading content onto the Veeva Vault platform, and overseeing internal processes and project management. This position is ideal for individuals with top-notch...


  • Warszawa, Mazovia, Polska Publicis Le Pont Pełny etat

    Job DescriptionAs a Regulatory Submission Specialist, you will be responsible for researching medical documents, identifying correct references for pharmaceutical marketing assets, submitting content into the Veeva Vault platform and maintaining internal processes and project management. This role is ideal if you possess strong organizational and...


  • Warszawa, Mazovia, Polska Zimmer Biomet Pełny etat

    Valued Team member: We are glad you are exploring new opportunities within Zimmer BiometWhat You Can ExpectAs a Regulatory Affairs Specialist for systems team, you provide support for the maintenance and implementation of RA systems, with a particular focus on Regulatory Information Management System (RIMS) and Regulatory Distribution Controls through SAP...

  • Senior Specialist

    2 tygodni temu


    Warszawa, Mazovia, Polska ING Bank N.V. Pełny etat

    We are looking for you if:You have a degree (MSc or PhD) in a quantitative/numerical field,You have minimum 3 years' of experience with credit risk models,You have knowledge of IRB and/or IFRS9 models and regulations,You have knowledge of statistical tools and modelling techniques,You have extensive programming experience in SAS or similar...


  • Warszawa, Mazovia, Polska Haleon Pełny etat

    Hello. We're Haleon, a leading consumer health company driven by the collective efforts of everyone who joins us. Together, we're dedicated to enhancing the daily health of billions worldwide. Through the growth and innovation of our top-tier brands like Sensodyne, Panadol, and Centrum, we combine profound human insights with trusted scientific methods. What...