[PPD Korea] RSM, CTC 정규직 추천채용
1. 회사소개 당사 PPD는 Global CRO(Contract Research Organization)회사로 강남구 역삼역 부근에 위치하고 있으며, 2005년도에 PPD 한국지사가 최초설립되어 16년의 역사를 가지고 있는 회사입니다. (본사/미국) 한국 임직원 수는 170명 이상으로(Global 총 직원 수/2만명 이상), 설립 이후부터 꾸준히 성장해 나가고 있는 회사입니다. 2. 모집 부문 [모집부문 1] : RSM(Remote Site Monitor)/0명 Hiring Requirements ？ Bachelor's Degree in a life science-related field or relevant/equivalent combination of education, training and experience that provides the individual with the required knowledge, skills, and abilities. ？ Prior clinical research experience(comparable to 0-1 year), as well as, knowledge of clinical monitoring through classwork/training that provides the required knowledge skills and abilities. Knowledge, Skills and Abilities ？ Effective clinical monitoring skills ？ Demonstrated understanding of medical/therapeutic area knowledge and medical terminology ？ Excellent understanding and demonstrated application of Good Clinical Practices and applicable Standard Operating Procedures ？ Effective oral and written communication skills, with the ability to communicate effectively with medical personnel ？ Strong customer focus ？ Effective interpersonal skills ？ Strong attention to detail ？ Effective organizational and time management skills ？ Proven flexibility and adaptability ？ Ability to work in a team or independently as required ？ Good computer skills: good knowledge of Microsoft Office and the ability to learn appropriate software ？ Good English language and grammar skills ？ Good presentation skills [모집부문 2] : CTC (Project Assistant)/ 0명 Essential Functions ？ Coordinates, oversees and completes administrative functions on assigned trials including, but not limited to,reviewing and transmitting regulatory documents, processing documents sent to file, QC and reconciling project reports, performing mass mailings and faxes, managing and distributing paper study supplies to sites. ？ Performs PPD Investigator file reviews and logs findings in CTMS. ？ Practices data stewardship by updating and maintaining assigned data points within CTMS in a timely fashion ？ Coordinates team conference calls, documents, completes and distributes meeting minutes from internal/client meetings. ？ Maintains a working knowledge of GCPs, PPD Global SOPs, applicable client SOPs and protocol-related specifics through professional career development to ensure investigative site regulatory compliance. ？ Serves as a resource to the project team. Education and Experience: ？ High School/ Secondary school diploma or equivalent and relevant formal education required. Bachelor’s Degree preferred or good general education, combined with evidenced administrative competence and relevant IT skills. In all cases, the combination of education, training and experience provides the individual with the required knowledge, skills and abilities to do the job. ？ Prior clinical research administrative experience, (comparable to at least 2 years). Insomecases,previous experience in a clinical environment where experience is gained in clinical trials, data management, medical terminology, medical research or health care or experience in a health sciences field with for maltraining in medical terminology and anatomy may be considered. Knowledge, Skills and Abilities ？ Self-motivated, positive attitude with effective oral and written communication andinterpersonal skills ？ Ability to work in a team or independently, as required ？ Good organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively ？ Demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency ？ Strong customer focus ？ Flexibility to reprioritize workload to meet changing project timelines ？ Demonstrated ability to attain and maintain a good working knowledge of applicable FDA ？ Regulations, ICH Good Clinical Practices, and PPD/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and close out. ？ Strong English language and grammar skills ？ Strong computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems ？ Ability to successfully complete PPD clinical training program 3. 근무조건 및 복리후생 - 급여: 내부규정에 따라 결정 - 연차 20일 발생, 병가(유급) 연 7개 발생, 3년 이상 근속 시 연차 3일 증가. | 
