5 Medical Affairs jobs in Qatar

Regulatory Affairs

Doha, Doha Premium Solutions Consultancy

Posted 2 days ago

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Job Description

Premium Solutions Consultancy is seeking a highly skilled and motivated Regulatory Affairs professional to join our team. As a Regulatory Affairs Specialist, you will be responsible for ensuring compliance with regulatory requirements and guidelines for our client projects. You will work closely with cross-functional teams to prepare and submit regulatory applications, maintain product registrations, and monitor regulatory changes.

Responsibilities

  • Prepare and submit regulatory applications, including product registrations and notifications
  • Coordinate with internal and external stakeholders to collect necessary documentation and information
  • Maintain up-to-date knowledge of relevant regulations and guidelines
  • Monitor and communicate changes in regulatory requirements that may impact our clients
  • Conduct regulatory assessments for new products and ensure compliance throughout the product lifecycle
  • Participate in regulatory agency inspections and audits
  • Collaborate with cross-functional teams to develop regulatory strategies and plans
  • Review and provide input on labeling and promotional materials to ensure compliance

Requirements

  • Bachelor's degree in a scientific or healthcare-related field
  • Minimum of 3 years of experience in regulatory affairs in the pharmaceutical, medical device, or biotechnology industry
  • Strong knowledge of local and international regulatory requirements and guidelines
  • Excellent communication and project management skills
  • Experience in preparing and submitting regulatory applications
  • Attention to detail and strong analytical skills
  • Ability to work independently and in a team environment
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Regulatory Affairs

Doha, Doha Premium Solutions Consultancy

Posted 14 days ago

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Job Description

Premium Solutions Consultancy is seeking a highly skilled and motivated Regulatory Affairs professional to join our team. As a Regulatory Affairs Specialist, you will be responsible for ensuring compliance with regulatory requirements and guidelines for our client projects. You will work closely with cross-functional teams to prepare and submit regulatory applications, maintain product registrations, and monitor regulatory changes. Responsibilities Prepare and submit regulatory applications, including product registrations and notifications Coordinate with internal and external stakeholders to collect necessary documentation and information Maintain up-to-date knowledge of relevant regulations and guidelines Monitor and communicate changes in regulatory requirements that may impact our clients Conduct regulatory assessments for new products and ensure compliance throughout the product lifecycle Participate in regulatory agency inspections and audits Collaborate with cross-functional teams to develop regulatory strategies and plans Review and provide input on labeling and promotional materials to ensure compliance Requirements Bachelor's degree in a scientific or healthcare-related field Minimum of 3 years of experience in regulatory affairs in the pharmaceutical, medical device, or biotechnology industry Strong knowledge of local and international regulatory requirements and guidelines Excellent communication and project management skills Experience in preparing and submitting regulatory applications Attention to detail and strong analytical skills Ability to work independently and in a team environment

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Medical Director Affairs & Strategy

CLIN BIOSCIENCES

Posted 3 days ago

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Job Description

Roles and Responsibilities

    • Lead all medical affairs activities including clinical support, scientific communication, KOL management, and regulatory interactions

    • Develop and implement medical strategy in alignment with global and regional business goals

    • Guide strategic planning for product launches, life cycle management, and market expansion

    • Collaborate with internal stakeholders R&D, regulatory, commercial, and pharmacovigilance teams

    • Represent the company in medical conferences, advisory boards, and external partnerships

    • Drive evidence generation through investigator-initiated trials, real-world data, and publications

    • Ensure compliance with all internal and external guidelines, SOPs, and industry regulations

    • Manage and mentor the medical affairs team to foster scientific excellence

Qualifications:
  • MD/MBBS/PhD in Medicine, Life Sciences, or a related field

  • 2-5+ years of experience in medical affairs, clinical development, or regulatory strategy

  • Previous leadership experience in a pharma/biotech/healthcare MNC is preferred

  • Understanding of therapeutic areas like Oncology, Immunology, Cardiology, or Rare Diseases will be advantageous

  • Interested to apply can share CV or call/WhatsApp to9342735755
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Medical Director Affairs & Strategy

Doha, Doha CLIN BIOSCIENCES

Posted 22 days ago

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Job Description

Roles and Responsibilities Lead all medical affairs activities including clinical support, scientific communication, KOL management, and regulatory interactions

Develop and implement medical strategy in alignment with global and regional business goals

Guide strategic planning for product launches, life cycle management, and market expansion

Collaborate with internal stakeholders R&D, regulatory, commercial, and pharmacovigilance teams

Represent the company in medical conferences, advisory boards, and external partnerships

Drive evidence generation through investigator-initiated trials, real-world data, and publications

Ensure compliance with all internal and external guidelines, SOPs, and industry regulations

Manage and mentor the medical affairs team to foster scientific excellence

Qualifications:

MD/MBBS/PhD in Medicine, Life Sciences, or a related field

2-5+ years of experience in

medical affairs, clinical development, or regulatory strategy

Previous leadership experience in a

pharma/biotech/healthcare MNC

is preferred

Understanding of therapeutic areas like Oncology, Immunology, Cardiology, or Rare Diseases will be advantageous

Interested to apply can share CV or call/WhatsApp to9342735755

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Medical director affairs & strategy

CLIN BIOSCIENCES

Posted today

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Job Description

permanent
Roles and Responsibilities
Lead all medical affairs activities including clinical support, scientific communication, KOL management, and regulatory interactionsDevelop and implement medical strategy in alignment with global and regional business goalsGuide strategic planning for product launches, life cycle management, and market expansionCollaborate with internal stakeholders R&D, regulatory, commercial, and pharmacovigilance teamsRepresent the company in medical conferences, advisory boards, and external partnershipsDrive evidence generation through investigator-initiated trials, real-world data, and publicationsEnsure compliance with all internal and external guidelines, SOPs, and industry regulationsManage and mentor the medical affairs team to foster scientific excellenceQualifications:MD/MBBS/Ph D in Medicine, Life Sciences, or a related field2-5+ years of experience inmedical affairs, clinical development, or regulatory strategyPrevious leadership experience in apharma/biotech/healthcare MNCis preferredUnderstanding of therapeutic areas like Oncology, Immunology, Cardiology, or Rare Diseases will be advantageousInterested to apply can share CV or call/Whats App to9342735755#J-18808-Ljbffr
This advertiser has chosen not to accept applicants from your region.
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