Senior Regulatory Affairs Associate

Parexel

. Provide local regulatory input to support regulatory strategies for new product registrations and lifecycle management activities .

Posted 11/11/2026full-timeRemote • TurkeySeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive expertise in Turkish regulatory affairs, including managing regulatory submissions and ensuring compliance with local and global regulatory requirements. Proficient in engaging with health authorities and coordinating regulatory documentation and activities.

Highest-signal resume keywords

Turkish Regulatory ExperienceRegulatory Submissions ManagementHealth Authority EngagementFluent in English and Local LanguageAdvanced Microsoft Office Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Regulatory StrategiesCompliance ManagementRegulatory Documentation PreparationPromotional Material ReviewLocal Legislation InterpretationRegulatory Information ManagementProduct Registration ProcessesLifecycle Management ActivitiesCross-Functional CoordinationTimelines Management

Soft Skills

Strong Communication SkillsOrganization SkillsTime Management SkillsProblem-Solving Skills

Industry Keywords

Health AuthorityRegulatory GuidelinesLocal Regulatory RequirementsIndustry DevelopmentsPolicy-Related ActivitiesTrade AssociationsRegulatory ApprovalsPost-Approval SubmissionsLabeling UpdatesTranslations

About the role

Key responsibilities & impact

Provide local regulatory input to support regulatory strategies for new product registrations and lifecycle management activities
Monitor and communicate regulatory progress to stakeholders
Ensure compliance with local regulatory requirements and participate in policy-related activities with industry groups and trade associations
Maintain current knowledge of local regulatory requirements, guidelines, and industry developments
Support interactions with health authorities, partners, vendors, and commercial colleagues
Prepare, organize, and coordinate local regulatory documentation and country-specific submission components
Maintain local regulatory systems in accordance with legislation
Support implementation and interpretation of local legislation and regulations
Conduct promotional material review activities and operational regulatory execution
Partner with regional regulatory teams on regulatory submissions
Represent regulatory interests for local commercial operations and communicate regulatory approvals
Maintain regulatory information management systems and monitor compliance activities
Support timely renewals, post-approval submissions, regulatory commitments, labeling updates, translations, and promotional material review
Participate in in-person meetings with relevant Health Authority representatives

Requirements

What you’ll need

Relevant bachelor's degree or equivalent secondary education in a scientific discipline such as biology, chemistry, or a related field with a pharmacological focus
5+ years of Turkish regulatory experience in a health authority-facing regulatory affairs role
Strong understanding of regional and global regulatory requirements, guidelines, and regulatory processes
Experience managing regulatory submissions, timelines, and cross-functional activities to support successful product registrations and compliance objectives
In-depth expertise in local health authority engagement and management
Strong communication, organization, time management, and problem-solving skills within a global environment
Fluent in the local language and English, both written and verbal
Advanced Microsoft Office skills

Benefits

Comp & perks

Health, Vision & Dental Insurance
Vacation/Holiday/Sick Time
Flexible benefit portal
Flexible work arrangements
Growth opportunities