직무 설명:
의 최신 채용 정보: ThermoFisher Scientific 직무 관련 CRA II. If the CRA II 의 공고 내용이 대한민국 귀하의 자격 요건과 일치한다면, 업데이트된 Jobkos 채용 포털을 통해 직접 최신 이력서를 제출해 주세요.
채용 지원 시 기업이 요구하는 특정 자격 요건을 충족해야 하므로 다소 시간이 걸릴 수 있습니다. 아래의 ThermoFisher Scientific 직무 관련 CRA II 채용 기회가 귀하의 역량과 일치하기를 바랍니다.
**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** Join Us as a Clinical Research Associate (Level II) - Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the 마지막 5 years. As part of our global team, you'll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix. What You'll Do: - Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable. - Participates in investigator meetings as necessary. Identifies potential - investigators in collaboration with the client 기업명 to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and retrieval of trial materials. - Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications. - Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System). - Facilitates effective communication between investigative sites, the client 기업명 and the PPD project team through written, oral and/or electronic contacts. - Responds to 기업명, client and applicable regulatory requirements/audits/inspections. - Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner. - Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members. - Contributes to other project work and initiatives for process improvement, as required. Education and Experience Requirements: - Bachelor's degree in a life sciences related fieldor a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification. - Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2 years as a clinical research monitor) or completion of PPD Drug Development Fellowship. - Valid driver's license where applicable. In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities: - Proven clinical monitoring skills - Demonstrated understanding of medical/therapeutic area knowledge and medical terminology - Demonstrated ability to attain and maintain a working knowledge of ICH GCPs, applicable regulations and procedural documents - Well-developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving - Ability to manage Risk Based Monitoring concepts and processes - Good oral and written communication skills, with the ability to communicate effectively with medical personnel - Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers' underlying issues - Good organizational and time management skills - Effective interpersonal skills - Attention to detail - Ability to remain flexible and adaptable in a wide range of scenarios - Ability to work in a team or independently as required - Good computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software - Good English language and grammar skills - Good presentation skills Working Conditions and Environment: - Work is performed in an office/ laboratory/clinical/and/or 홈 office environment with exposure to electrical office equipment. - Frequent drives to site 위치s. Frequent travel, generally 60-80% but more for some individuals. May also include extended overnight stays. - Exposure to biological fluids with potential exposure to infectious organisms. - Personal protective equipment required such as protective eyewear, garments and gloves. - Exposure to fluctuating and/or extreme temperatures on rare occasions Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
채용 상세 정보:
- 기업명: ThermoFisher Scientific
- 직무: CRA II
- 근무 장소: 대한민국
- 국가: KR
지원 방법:
채용 정보에 기재된 자격 요건 및 최소 학력 사항을 확인하신 후, CRA II at the office 대한민국 로 자기소개서, 이력서(CV), 졸업증명서 사본 및 기타 증빙 서류를 준비해 주시기 바랍니다. 아래의 '다음 페이지' 링크를 통해 제출하세요.
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