CTM(Lead CRA)

SUMMARYI am currently helping for a medium sized global CRO looking for experienced Lead CRA/CTM in Seoul. The business have recently won a CRO Leadership Award in the categories Quality!As Lead CRA, you will provide clinical oversight for full-service global projects in Korea.

You will lead study start-up, clinical monitoring, and site management activities while serving as the main point of contact for internal stakeholders and project teamsRESPONSIBILITIESCoordinate site feasibility, investigator identification, and study start-up Monitor project timelines, enrollment metrics, and implement corrective actions Review and ensure compliance of monitoring visit reports across the region Support CRAs in resolving queries, including Central Monitoring observations Oversee protocol deviation reporting, safety info flow, and clinical supplies Maintain timely updates to corporate and study-specific tracking systems Act as liaison between CRA teams, Site Management Associates, and PMs Conduct and supervise monitoring visits, site audits, and CAPA activities Lead project team meetings and provide country-level status updates Deliver project-specific training and support investigator meeting presentations Manage data integrity, risk, and documentation across Korean trial sites Supervise investigational product handling and site-level ISF/TMF reconciliation QUALIFICATIONSDegree in Life Sciences, Medicine, Pharmacy, or Nursing (MD, MPharm, RN, or equivalent) Minimum 5 years of monitoring experience with global trials and prior Lead CRA responsibilities Deep knowledge of Korean regulatory landscape and clinical site management Experience across all monitoring visit types (SIV, IMV, COV)Therapeutic expertise in:

Oncology (strongly preferred)GI disorders (Crohn’s, Ulcerative Colitis, IBS)Cell & Gene Therapies (CAR-T, Radiopharmaceuticals, etc. ) Strong planning, multitasking, and problem-solving abilitiesFull professional proficiency in English Proficiency in MS Office tools (Word, Excel, PowerPoint)Proven ability to lead teams, collaborate cross-functionally, and deliver on timelines DURATIONPermanent, full-timeSALARYAttractive salary plus benefitsLOCATIONSeoulABOUT PLANET PHARMAPlanet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London.

We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including:

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. www. planet-pharma. comABOUT PLANET PHARMAPlanet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London.

We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including:

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. www. planet-pharma. comTO APPLYPlease click ‘apply’ or contact Steven Fan (Recruiter, APAC) at Planet Pharma for more information: E: steven. fan@planet-pharma. co. ukT: : +61 370427282Linkedin: https: //www. linkedin. com/in/steven-fan-38a394128/