Regulatory Affairs Job at ClinChoice, Armenia | Life Sciences | Apply Now
If you are an aspiring compliance professional or a recent life sciences graduate looking to launch an international corporate career, this full-time position at ClinChoice is an exceptional opportunity. Located in the fast-growing operational hub of Yerevan, Armenia, this role offers hands-on exposure to global market authorization and registration pipelines. For organized graduates searching for a high-trajectory Regulatory Affairs Job, this entry-to-junior position provides direct training in dossier publishing, Health Authority (HA) query tracking, and labeling quality control. It serves as an elite launchpad for a long-term ClinChoice career and stands out as a premier Life Science Job in the Eastern European and Eurasian clinical development sectors.
- Job Position: Associate, Regulatory Affairs
- Location: Yerevan, Armenia
About The Company
ClinChoice is a leading, global full-service Contract Research Organization (CRO) specializing in clinical development and functional solutions for the pharmaceutical, biotechnology, medical device, and consumer health industries. With over 28 years of proven delivery, ClinChoice manages a global network of more than 4,000 professionals across 20+ countries throughout the Americas, Europe, and the Asia-Pacific region. The company boasts a below-industry-average turnover rate, driven by a quality-focused “one-team” culture that prioritizes continuous training, close management mentorship, and a healthy work-life balance. ClinChoice operates as an equal-opportunity employer that views demographic diversity—across gender, race, beliefs, and ethnicities—as its core organizational strength.
Regulatory Affairs Job – Key Responsibilities
As a Regulatory Affairs Associate, you will support the in-house team in executing regulatory submissions and maintaining accurate documentation across a diverse portfolio of medicinal products, medical devices, cosmetics, and food supplements.
Your day-to-day coordination, data, and compliance duties will include:
- Dossier Preparation & Follow-Up: Supporting new applications for marketing authorizations, lifecycle variations, and product renewals, while tracking Health Authority (HA) queries closely through to final approval.
- Publishing & Submission: Formatting, indexing, compiling, and publishing formal product registration dossiers for local and international regulatory agency review.
- Database & Information Archival: Coordinating database tracking systems to ensure all global product registration records remain fully accurate, current, and archived according to standard operating procedures.
- Packaging & Labeling Design: Specifying explicit storage, labeling, and structural packaging requirements for highly regulated consumer health and pharmaceutical products.
- Quality Control Audits: Creating, updating, reviewing, and performing rigorous quality checks (QC) on product labels and instructions for use (IFU) to advance this Regulatory Affairs Job.
- Cross-Functional Collaboration: Partnering with international clinical operations and manufacturing teams to ensure regulatory alignment and satisfy a fast-paced Life Science Job workflow.
Qualifications & Candidate Profile For Regulatory Affairs Job
This position is tailored for highly motivated individuals with an analytical mindset who are eager to translate their scientific degrees into a specialized corporate compliance career.
- Required Criteria:
- Educational Foundation: A formal Bachelor’s Degree in a Life Science discipline (such as Biology, Biomedical Engineering, or a related quantitative healthcare field).
- Linguistic Mastery: Full fluency in English (written, verbal, and reading comprehension) is mandatory to operate within ClinChoice’s global matrix environment.
- Core Competencies: Strong team-player traits, exceptional organizational habits, sharp attention to detail, and the ability to work effectively under pressure to meet tight project deadlines.
- Preferred Assets:
- Prior internship, academic research track, or entry-level work experience in regulatory affairs, clinical documentation, or quality assurance is a plus but not required.
- Proficiency with standard digital database tools, electronic spreadsheets (Microsoft Excel), and document management software.
In short, the Regulatory Affairs Associate position at ClinChoice is a definitive route to transitioning your scientific background into a highly marketable, international compliance asset. Securing this role allows you to move past repetitive laboratory testing and gain firsthand mastery over the health authority filings, dossier publishing mechanics, and labeling quality controls that dictate how medical innovations enter the global marketplace. If you live in or are willing to relocate to Yerevan, hold a life sciences degree, and want to establish a career with a premier global CRO, apply today to lock in this opportunity.
