Regulatory Affairs Job at ClinChoice, Armenia | Life Science | Apply Online
If you are an early-career life scientist, an analytical technician, or a recent biochemistry graduate looking to step away from repetitive wet-lab environments and into international corporate compliance, this full-time vacancy is an exceptional opportunity. Located at ClinChoice’s operational base in Yerevan, Armenia, this permanent in-house position places you at the center of regional and global market access pipelines. For detail-oriented graduates searching for a high-value Regulatory Affairs Job, this role offers direct, practical exposure to Marketing Authorization applications, health authority queries, and global product labeling quality checks. It serves as an elite launchpad to build a long-term ClinChoice career and stands out as a premier choice for anyone looking to secure a foundational, highly compliant Life Sciences Job within a rapidly growing global Contract Research Organization (CRO).
- Job Position: Associate, Regulatory Affairs
- Location: Yerevan, Armenia
About The Company
ClinChoice is a leading, global full-service CRO specializing in clinical development and high-efficiency functional solutions for international pharmaceutical, biotechnology, medical device, and consumer health companies. Backed by over 28 years of high-quality delivery, ClinChoice manages an international network of over 4,000 professionals spanning more than 20 countries across the Americas, Europe, and the Asia-Pacific region. Operating under a collaborative “one-team” culture, ClinChoice balances an emphasis on professional development with an excellent work-life balance, resulting in employee turnover rates well below the standard industry average. Joining the Yerevan regulatory division means stepping into an inclusive company culture where continuous, structured management training keeps personnel highly qualified in the exact methodologies needed to clear innovative treatments for commercial markets safely.
Regulatory Affairs Job – Key Responsibilities
The Associate, Regulatory Affairs functions as an essential compliance engine, assisting with the compilation, submission, and quality checking of official technical files required by regional Health Authorities (HA).
Your core dossier curation, registration tracking, and packaging validation duties include:
- Marketing Authorization Support: Assisting with compiling, reviewing, and drafting new applications, renewals, and variation dossiers for medicinal products, medical devices, cosmetics, and food supplements to advance this Regulatory Affairs Job.
- Dossier Publishing & Submission: Actively publishing and submitting product registration applications to targeted regulatory portals, while following up closely on technical queries from Health Authorities through to formal approval.
- Database & Information Coordination: Coordinating cross-functional activities to ensure that all internal product registration databases, tracking tables, and regulatory milestones are kept completely accurate and current.
- Information Archival Curation: Supporting the indexing, meticulous tracking, and long-term archival of critical regulatory intelligence documentation to support your ClinChoice career.
- Packaging Specification Validation: Specifying exact legal storage, labeling, and protective packaging requirements for diverse classes of regulated consumer and clinical products.
- Product Label Quality Auditing: Taking direct responsibility for the creation, regular updating, technical review, and structural quality checks of product labels, ensuring complete compliance with local consumer safety legislation.
Qualifications & Profile Requirements For Regulatory Affairs Job
ClinChoice seeks a dynamic, highly organized team player who can demonstrate a proactive approach to technical documentation and maintain complete accuracy under tight deadlines.
- Required Academic Criteria:
- Educational Foundation: A completed formal Bachelor’s Degree in a Life Science discipline (such as Biology, Biomedical Engineering, or a closely related natural scientific field) to qualify for this competitive Life Sciences Job.
- Essential Skills & Competencies:
- Linguistic Mastery: Full professional fluency in written and verbal English is mandatory to draft international reports and collaborate across global project divisions.
- Exceptional attention to detail, strong organizational habits, and a highly analytical approach to sorting complex regulatory texts.
- Proven capability to work effectively under pressure and adjust priorities smoothly to meet strict regulatory health authority submission deadlines.
- Strong interpersonal communication skills and an enthusiasm for active, multi-disciplinary teamwork.
- Preferred Technical Asset: Prior professional experience or internship exposure within a regulatory affairs, clinical research, or pharmaceutical compliance setting is a distinct advantage but not strictly required.
In short, the Associate, Regulatory Affairs position at ClinChoice is a definitive route to transitioning your life sciences degree into a premium global asset. Securing an appointment here allows you to bypass general laboratory bench production loops and take direct operational charge of the marketing authorizations, label quality checks, and health authority alignments that clear innovative therapeutics for global markets. If you reside in or can commute to Yerevan, meet the baseline science requirements, and possess a zero-error approach to document tracking, apply today to secure this premier Regulatory Affairs Job, launch a highly rewarding ClinChoice career, and lock in this outstanding Life Sciences Job.
