Opportunité de Carrière : Lead Clinical Research Associate chez PSI CRO

Présentation de L’Entreprise

PSI CRO, fondée en 1995, est une entreprise mondiale reconnue pour son engagement envers ses employés et la qualité de son travail. Avec une équipe de 3 000 professionnels passionnés, PSI CRO œuvre à la frontière de la science médicale, contribuant activement à l’évolution des traitements médicaux. La société se distingue par son approche organique de l’expansion, passant de quelques pays à une présence mondiale tout en maintenant des normes élevées.

Description du Poste

En tant que Lead Clinical Research Associate, le candidat choisi supervisera les aspects cliniques des projets globaux en Corée. Ce rôle stratégique implique la gestion des communications avec les parties prenantes des projets et la garantie de la réussite des essais cliniques dans divers domaines thérapeutiques. La personne retenue sera responsable de la mise en œuvre de procédures rigoureuses avec un accent sur la qualité.

Responsabilités Principales

Les tâches incluent, sans s’y limiter :

• Coordonner le processus d’évaluation des sites et les activités de démarrage des études.
• Surveiller les délais des projets et l’inscription des patients, et mettre en œuvre des mesures correctives.
• Gérer la conformité et résoudre les observations relevées par la supervision clinique.
• Assurer la communication fluide entre les différents intervenants.
• Participer aux visites de préparation d’audit et coordonner la résolution des problèmes identifiés.
• Former et encadrer les nouveaux Lead CRAs.

Compétences et Qualifications

Les candidats doivent posséder :

• Un diplôme pertinent (MD, MPharm, RN ou équivalent) et au moins 5 ans d’expérience en surveillance de sites.
• Une connaissance approfondie des réglementations coréennes et des pratiques de recherche clinique.
• Une expérience spécifique dans les domaines oncolologiques et thérapeutiques avancés (CAR-T, thérapies géniques, etc.).
• Une maîtrise de l’anglais et des compétences en informatique.

Environnement de Travail et Avantages

PSI CRO se distingue par son engagement envers le bien-être de ses employés. Le cadre de travail est dynamique et favorise un équilibre sain entre vie professionnelle et personnelle. Les avantages incluent :

• Une organisation de travail flexible.
• Un soutien pour la formation en anglais.
• Des installations sur site, y compris des espaces de détente.
• Des primes basées sur la performance et d’autres avantages sociaux.

Postuler

Si cette opportunité vous intéresse, n’hésitez pas à postuler à travers le lien suivant : Postulez dès maintenant !

Conclusion

Rejoindre PSI CRO représente une volonté de faire une différence dans la vie des patients à l’échelle mondiale. Les candidats sont encouragés à postuler et à contribuer à une entreprise qui valorise son personnel et son engagement envers l’innovation et la qualité.

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📅 Date de publication de l’offre : Tue, 01 Jul 2025 22:59:16 GMT

🏢 Entreprise : PSI CRO

📍 Lieu : 서울시

💼 Intitulé du poste : Lead Clinical Research Associate

💶 Rémunération proposée :

📝 Description du poste : Company DescriptionWe are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.We offer an inspiring story of the company that has grown organically from a handful of countries to global presence. PSI is a mature company with standards and practices, but we do not stand still. Every day, there is a figurative Everest to climb, and you will not get bored here.Job DescriptionWe’re searching for a knowledgeable, team-oriented, and proactive leader to supervise the clinical aspects of full-service global projects in Korea. As a Lead CRA at PSI, you will work on the frontline of communication with project stakeholders, ensuring the successful conduct of clinical trials in a variety of therapeutic indications. You will maintain the highest quality standards in the industry, while performing and supervising study start-up, clinical monitoring and site management activities on the country/regional level.Location: Hybrid in SeoulResponsibilities:

• Coordinates investigator/ site feasibility and identification process, as well as study startup.
• Monitors project timelines and patient enrollment, implements respective corrective and preventive measures.
• Reviews monitoring visit reports for all visit types and ensures reporting compliance of the Monitors in the region.
• Manages Monitors in the query resolution process, including Central Monitoring observations.
• Coordinates safety information flow and protocol/process deviation reporting.
• Performs clinical supplies management with vendors on a country and regional level.
• Ensures study-specific and corporate tracking systems are updated in a timely manner.
• Acts as the main communication line between Monitor, Site Management Associate, Regional Project Lead, and/ Project Manager.
• Coordinates planning of supervised monitoring visits and conducts the visits.
• Manages the project team in site contracting and payments.
• Leads project team calls on a country level as well as provides status updates and reports to Regional Lead/ Project Manager.
• Ensures ongoing evaluation of data integrity and compliance at a country/regional level.
• Conducts site audit preparation visits, may participate in site audits, and coordinates resolution of site audit findings on a country/regional level.
• Oversees project team in CAPA development and implementation.
• Coordinates project team in process deviations review, management and reporting.
• Conducts initial training and authorization monitoring visits for Monitors and acts as a mentor for newly promoted Lead CRAs.
• Provides project-specific training and prepares training materials for the project team under supervision of a Project Manager and Regional Project Lead.
• Delivers trainings and presentations at Investigator Meetings.
• Prepares, conducts and reports site selection, initiation, routine monitoring and closeout visits.
• Ensures that subject recruitment targets and project timelines are properly defined, communicated, recorded, and met at site level.
• Ensures accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations.
• Supervises source data verification and follows up on data queries at site level in the country/region; reviews and manages study risks on a site level.
• Ensures proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and clinical study supplies on a country/region level.
• Reviews essential study documents and supervises reconciliation of study Investigator Site File (ISF) / TMF at site level and country/region level.
• Ensures data integrity and compliance at a site level.
• Supervises Site Management Associates in the flow of documents and laboratory supplies between the site and the Central/ Regional Lab/ Central Reviewer.
• Conducts project-specific training of site Investigators.
• Supports preparation of draft regulatory and ethics committee submission packages.

Qualifications

• Relevant educational background, such as MD, MPharm, RN or College/University degree in Life Sciences or an equivalent combination of education, training and experience.
• Minimum of 5 years’ site monitoring experience with participation in global clinical projects as a Lead Monitor.
• Must have prior experience monitoring or managing sites and CRAs in Korea with knowledge of Korean regulatory guidelines and practices.
• Experience with all types of monitoring visits in Phases I-III.
• Strong experience in Oncology preferred.
• Experience in CAR-T Therapy or other types of Cell Therapy, Gene Therapy, Radiation Therapy or Radiopharmaceuticals, or Nuclear Medicine is preferred.
• Strong experience in GI (Chron’s, Ulcerative Colitis, IBS) preferred.
• Full working proficiency in English.
• Proficiency in MS Office applications.
• Ability to plan, multitask and work in a dynamic team environment.
• Excellent Communication, collaboration, and problem-solving skills

Additional InformationTake the next step in your career and join a company that genuinely focuses on its people.About UsPSI is a passionate, organically grown, and award-winning full-service CRO who dares to be different. As a dynamic and global company, we bring together more than 3000 driven and dedicated experts across 60 countries working collectively to help make a positive impact on patient lives.How are we different?PSI is privately owned by the very people who founded the company 30 years ago, and they’re still working here today. As a result, we have grown organically around the globe and have kept our company fully independent, giving us significant advantages and freedoms.Being a Part of the TeamAs a part of the PSI team, you will have a fair degree of ownership and autonomy to make nuanced country-and department-specific adjustments while nurturing the global PSI culture that unites us across six continents.You will receive continuous support from your global peers and join a fast-paced, innovative, and results-oriented working environment with lean communication lines. We pride ourselves on being approachable, receptive to new ideas, and open to feedback.Growth OpportunitiesPSI is proud to invest in our people, from entry-level team members to senior leaders, helping you identify and hone your unique strengths at every step of your career. From on-the-job learning experiences to formal development programs, our professionals have a variety of opportunities to continue to grow throughout their career.At our Korean office, we are committed to fostering employee well-being and promoting healthy work-life balance. We strive to create a positive and rewarding environment where our team members can grow and succeed.Remuneration will reflect your skills, experience, expectations, and potential contribution. Our comprehensive benefit package includes:

• Flexible work arrangement
• English training support
• Onsite facilities, including yoga room, break room, lounge
• Group term insurance
• Holiday gifts and leaves
• Long service awards
• Performance-based annual bonus and incentive

➡️ Candidater en ligne

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