Mlr (Medical/legal/regulatory) Specialist

hace 3 días


Buenos Aires, Buenos Aires C.F., Argentina Mondelēz International A tiempo completo
Mlr (Medical/legal/regulatory) Specialist

Viseven Group is an international IT company specialising in interactive content and cloud-based solutions for global pharmaceutical companies since 2009; constant growth and self-development is in our corporate DNA. Our unique developments and approaches are actively used in more than 50 countries all over the world. Viseven's solutions are represented at major industry events in Barcelona, Philadelphia, London, etc.

Role description: As the MLR Specialist, you will be responsible for supporting the appropriate review of omnichannel marketing communications materials (advertising, training, promotional). Communications with divisional teams, providing consultative and tactical support, serving as a liaison for all individuals within the approval process, and aiding in divisional compliance.

Responsibilities:

  1. Assurance of MLR review process expertise to help set vision and direction in partnership with other Commercial business partners to support business priorities and maintain the health of the MLR review environment.
  2. Oversees and participates in developing comprehensive onboarding and refresher training programs for all stakeholder groups — content owners/creators, reviewers/approvers, and end users.
  3. Establishes and guides strategic understanding of process KPIs and timelines to drive the process and system's improvement, efficiency, and effectiveness.

Required skills & knowledge:

  1. Medical, pharmaceutical, or biology education.
  2. Minimum 3 years of experience in a highly regulated environment - MLR (Advertising Committee), experience in a medical, pharmaceutical, or healthcare field.
  3. Knowledge of the specifics of MLR requirements for the USA market.
  4. Knowledge of a modular approach to content creation will be an added benefit.
  5. Adaptable, open to change, and able to work in challenging situations.
  6. Outstanding interpersonal, teamwork, and communication skills.
  7. Ability to proactively manage workload and prioritize in a rapidly changing environment.
  8. Ability to navigate systems and processes.
  9. Ability to work independently and be self-motivated.
  10. Fluent in English (speaking and writing).

What we provide: We understand that our team members are essential to making our goals a reality, so we value and empower them to share their vision. And we reward this kind of passion with a highly competitive compensation and exceptional benefits, such as:

  1. Competitive compensation and regular performance-based salary and career development reviews.
  2. Passionate experienced team, friendly atmosphere.
  3. Professional and career growth.
  4. Paid time off - 18 business days per year (20 business days after 2 years of cooperation).
  5. Non-documented sick leave - 4 business days per year.
  6. Documented sick leave - 20 business days per year.
  7. Family leave - 3 paid business days in case of marriage, childbirth or bereavement.
  8. Comprehensive medical insurance compensation.
  9. English learning courses.
#J-18808-Ljbffr

  • Buenos Aires, Buenos Aires C.F., Argentina Scaledon A tiempo completo

    Mlr (Medical/legal/regulatory) SpecialistViseven Group is an international IT company specialising in interactive content and cloud-based solutions for global pharmaceutical companies since 2009; constant growth and self-development is in our corporate DNA. Our unique developments and approaches are actively used in more than 50 countries all over the world....

  • MLR Review Specialist

    hace 2 días


    Buenos Aires, Buenos Aires C.F., Argentina Scaledon A tiempo completo

    We are looking for a highly skilled MLR Specialist to join our team at Scaledon. As a key member of our team, you will be responsible for ensuring compliance with regulatory requirements and developing effective MLR review processes.Responsibilities and RequirementsResponsibilities:Develop and implement MLR review processes to ensure compliance with...


  • Buenos Aires, Buenos Aires C.F., Argentina Mondelēz International A tiempo completo

    As a Medical Regulatory Specialist at Viseven Group, you will be responsible for ensuring the accuracy and compliance of marketing communications materials. You will work closely with divisional teams to provide consultative and tactical support, serving as a liaison for all individuals within the approval process.The role involves overseeing and...


  • Buenos Aires, Buenos Aires C.F., Argentina Scaledon A tiempo completo

    Viseven Group is a leading IT company that has been specializing in interactive content and cloud-based solutions for global pharmaceutical companies since 2009.Job DescriptionAs the MLR Specialist, you will play a crucial role in supporting the review of omnichannel marketing communications materials. You will be responsible for communicating with...


  • Buenos Aires, Buenos Aires C.F., Argentina Scaledon A tiempo completo

    Scaledon is an international IT company that offers innovative solutions for the pharmaceutical industry. We are seeking a highly skilled MLR Specialist to join our team.Job ResponsibilitiesThe successful candidate will be responsible for reviewing and approving omnichannel marketing communications materials. They will work closely with divisional teams to...


  • Buenos Aires, Buenos Aires C.F., Argentina Scaledon A tiempo completo

    At Scaledon, we are committed to delivering high-quality solutions to the pharmaceutical industry. We are seeking a highly skilled MLR Specialist to join our team and contribute to our success.Key ResponsibilitiesThe successful candidate will be responsible for developing and implementing MLR review processes to ensure compliance with regulatory...


  • Buenos Aires, Buenos Aires C.F., Argentina Mondelēz International A tiempo completo

    Viseven Group is an international IT company specialising in interactive content and cloud-based solutions for global pharmaceutical companies since 2009. Our unique developments and approaches are actively used in more than 50 countries worldwide.We are seeking a Healthcare Review Manager to join our team. As a key member of our regulatory compliance team,...


  • Buenos Aires, Buenos Aires C.F., Argentina EBANX A tiempo completo

    At EBANX, we are dedicated to providing global access for everyone. As a Senior Regulatory Analyst based in Argentina, you will play a critical role in ensuring our operations remain compliant with Argentine and regional LATAM regulations.Key Responsibilities:Partner Relations: Develop strong relationships with strategic partners, regulatory bodies, and...


  • Buenos Aires, Buenos Aires C.F., Argentina Cabify A tiempo completo

    We are currently seeking a Regulatory Affairs Specialist to join our team. As a Regulatory Affairs Specialist, you will be responsible for ensuring that all clinical trials are conducted in accordance with regulatory requirements and industry standards. This includes reviewing and implementing regulatory strategies, conducting regulatory inspections, and...


  • Buenos Aires, Buenos Aires C.F., Argentina Siemens S.A. A tiempo completo

    About Our Team: At MURAL, we're passionate about empowering teams to connect and innovate. As a Compliance Specialist, you will be responsible for ensuring that our products and services meet the highest standards of compliance and regulatory requirements.\You will be the primary point of contact for compliance related requests from customers, and will work...


  • Buenos Aires, Buenos Aires C.F., Argentina Ebanx Group A tiempo completo

    Ebanx Group is the leading payment platform connecting global companies with customers from the fastest-growing digital markets in Latin America.We're on a mission to provide global access for everyone. We believe that transforming challenges into opportunities and making the impossible part of the journey is crucial.We created a payment technology that...


  • Buenos Aires, Buenos Aires C.F., Argentina Mondelēz International A tiempo completo

    We are seeking a Clinical Trials Coordinator to join our team. As a key member of our regulatory compliance team, you will be responsible for coordinating clinical trials and ensuring compliance with regulatory requirements. You will work closely with divisional teams to provide consultative and tactical support, serving as a liaison for all individuals...


  • Buenos Aires, Buenos Aires C.F., Argentina Mondelēz International A tiempo completo

    We value our team members and offer exceptional benefits. As a Medical Regulatory Specialist at Viseven Group, you will receive competitive compensation and regular performance-based salary and career development reviews. You will also have access to passionate experienced team members, friendly atmosphere, professional and career growth opportunities, paid...


  • Buenos Aires, Buenos Aires C.F., Argentina SAP A tiempo completo

    About the RoleWe are seeking a highly skilled Regulatory Operations Specialist to join our team. As a key member of our operations group, you will be responsible for ensuring compliance with regulatory requirements and facilitating the activation of investigative sites.This role involves working closely with internal stakeholders to provide guidance on local...


  • Buenos Aires, Buenos Aires C.F., Argentina PUMA A tiempo completo

    Regulatory Affairs Project Management SpecialistJohnson & JohnsonREGULATORY AFFAIRS PROJECT MANAGEMENT SPECIALIST: At Johnson & Johnson, the largest healthcare company in the world, we come together for one purpose: to transform the history of health in humanity. Diversity & Inclusion are essential to continue building our history of pioneering and...


  • Buenos Aires, Buenos Aires C.F., Argentina Bitfinex A tiempo completo

    Founded in 2012, Bitfinex is a leading digital asset trading platform offering cutting-edge services for global liquidity providers and crypto-asset traders. We're at the forefront of financial evolution, shaping the future of decentralized finance.Job Description:This role offers an exciting opportunity to join our Regulatory and Licensing team as an...


  • Buenos Aires, Buenos Aires C.F., Argentina Dana TM4 A tiempo completo

    About the RoleWe are seeking a highly skilled and experienced Global Regulatory Affairs Specialist to join our team in LATAM. This is an exciting opportunity for a talented professional to shape the vision and goals for Global Regulatory Affairs and Seqirus by providing specialist, regional advice and support.Key ResponsibilitiesPartner with other functions...


  • Buenos Aires, Buenos Aires C.F., Argentina Bitfinex A tiempo completo

    Founded in 2012, Bitfinex is a digital asset trading platform offering state-of-the-art services for digital currency traders and global liquidity providers. We're on a mission to create the most innovative cryptocurrencies exchange. This is a unique opportunity, a rare window of time at the tipping point of financial evolution. Much like the early days of...


  • Buenos Aires, Buenos Aires C.F., Argentina Puma A tiempo completo

    Regulatory Affairs Project Management SpecialistJohnson & JohnsonREGULATORY AFFAIRS PROJECT MANAGEMENT SPECIALIST: At Johnson & Johnson, the largest healthcare company in the world, we come together for one purpose: to transform the history of health in humanity.Diversity & Inclusion are essential to continue building our history of pioneering and...


  • Buenos Aires, Buenos Aires C.F., Argentina Ebanx group A tiempo completo

    EBANX is the leading payment platform connecting global companies with customers from the fastest-growing digital markets in the world.Since the beginning of our journey, we have had one mission: to provide global access for everyone. We believe that transforming challenges into opportunities and making the impossible part of the journey is crucial That's...