11에서 최고의 software specialization, sr staff 채용공고 11개(지금 채용 중!)

Sr. CRA 1
Fortrea —서울
- 정규직
Korea Communications Manager
Microsoft —서울
- 정규직
22시간
DRAM Circuit Design, Staff
Qualcomm —서울
Senior PIDS Support Engineer
Ericsson —서울
3일
Senior Manager, Sales
Arrow Electronics, Inc. —서울
4일
VP, Finance Control (Korea)
Nomura —서울
2일
Senior CRA
JBlab —서울
Senior Designer - Fire Engineer
Jensen Hughes —서울
Technical Support Analyst – Workstation Support Analyst
Visa International Asia Pacific Korea, Ltd. —서울 을지로5길
- 정규직
빠른 지원하기
[Coupang Pay] Director, Back-End Engineering
Coupang —서울
빠른 지원하기
Client Advisor, Korea
Christie's —서울
- 정규직
9시간

More jobs to discover

Find similar jobs that you might be interested in.

Engagement Manager, gTech Ads (English, Korean)
구글코리아 —서울
Google, 광고 기술 전문 조직 'gTech Ads'의 Engagement Manager 경력직 채용에 나선다 Google이 서울을 근무지로 하는 gTech Ads 부문의 Engagement Manager 경력직 채용을 진행할 예정이다. 이번 채용은 Google의 주요 광고…
Industry Manager, Consumer/Commerce (Korean, English)
구글코리아 —서울
Google, 서울 오피스에서 Consumer/Commerce 분야 Industry Manager 채용 Google이 서울 오피스에서 Consumer/Commerce 분야의 Industry Manager(Mid-level) 채용을 진행할 예정이다. 이번 채용은 한국의 주요 광고주 및…

Show more similar jobs

11의 software specialization, sr staff에 대한 최신 취업소식을 받고 싶습니다.

계정에 로그인하면 SimplyHired의 서비스 이용약관과 쿠키 및 개인정보 취급방침에 동의하는 것입니다.

더 많은 지역의 채용공고 둘러보기

software specialization, sr staff jobs near 11

서울 지역 Technical Project Manager 채용공고

서울 지역 Business Systems Analyst 채용공고

서울 지역 Interior Design 채용공고

서울 지역 Ai Ml Engineer 채용공고

서울 지역 Cloud Engineer 채용공고

경기도 이천 지역 Process Engineer 채용공고

화성 동탄면 지역 Service Engineer 채용 채용공고

서울 지역 Back End 개발 채용공고

하남 감일동 지역 Backend Developer 채용공고

서울 지역 React Developer 채용공고

서울 지역 Hotel, Director Of Sales Marketing 채용공고

서울 지역 Client Manager 채용공고

서울 지역 Medical Advisor 채용공고

서울 지역 Business Advisor 채용공고

성남 금광동 지역 Clinical 채용공고

서울특별시 지역 Clinical Trial 채용공고

Sr. CRA 1

Fortrea -
서울

지금 지원하기

채용공고 세부정보

정규직

상세 직무 내용

Job Overview:

The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans, as assigned. Function as leader for projects of limited scope, as assigned. Assume line management responsibilities, as assigned. Act in the project role of a Local Project Coordinator or Lead CRA as assigned.

Summary of Responsibilities:

The statements below are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills, and duties.
Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned.
Responsible for all aspects of site management as prescribed in the project plans.
General On-Site Monitoring Responsibilities:
Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study.
Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.
Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review.
Monitor data for missing or implausible data.
Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Fortrea travel policy.
Ensure audit readiness at the site level.
Travel, including air travel, may be required and is an essential function of the job.
Prepare accurate and timely trip reports.
Manage small projects under the direction of a Project Manager/Director as assigned.
Serve as lead monitor for a protocol or project and may assist in establishing monitoring plans and trip report review as assigned.
Review progress of projects and initiate appropriate actions to achieve target objectives.
Organize and make presentations at Investigator Meetings.
Participate in the development of protocols and Case Report Forms as assigned.
Participate in writing clinical trial reports as assigned.
Interact with internal work groups to evaluate needs, resources, and timelines.
Act as contact for clinical trial supplies and other suppliers (vendors) as assigned.
Responsible for all aspects of registry management as prescribed in the project plans.
Undertake feasibility work when requested.
Conduct, report, and follow-up on Quality Control (QC) visits when requested.
Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor as assigned.
Negotiate study budgets with potential investigators and assist the Fortrea legal department with statements of agreements as assigned.
Track and follow-up on Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.
Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management.
Assist with training, mentoring and development of new employees, e.g., co-monitoring.
Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned 29) Perform other duties as assigned by management.
All other duties as needed or assigned.

Qualifications (Minimum Required):

University or college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing certification, medical or laboratory technology.
In lieu of the above education requirement, candidates with a minimum of 3 years relevant clinical research experience in pharmaceutical or CRO industries will be considered.
Thorough knowledge of regulatory requirements including a basic understanding of regulatory requirements in other countries.
Thorough understanding of the drug development process.
Fluent in local office language and in English, both written and verbal.
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Experience (Minimum Required):

Three (3) years of Clinical Monitoring experience.
Have a full understanding of Serious Adverse Event (SAE) reporting, process production on reports, narratives and follow up of SAEs.
Advanced site monitoring skills.
Advanced study site management skills.
Advanced registry administration skills.
Ability to work with minimal supervision.
Good planning and organization skills.
Good computer skills with good working knowledge of a range of computer packages.
Advanced verbal and written communication skills.
Ability to train and supervise junior staff.
Ability to resolve project-related problems and prioritizes workload for self and team.
Ability to work within a project team.
Works efficiently and effectively in a matrix environment.
Valid Driver's License.

Preferred Qualifications Include:

One (1) or more year's additional experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred.
Local project coordination and/or project management experience.

Physical Demands/Work Environment:

Travel requirements: 60-80% overnight.

Learn more about our EEO & Accommodations request here .

지금 지원하기

검색결과 새로고침

11 지역 채용공고 software specialization, sr staff건

Sr. CRA 1

Korea Communications Manager

DRAM Circuit Design, Staff

Senior PIDS Support Engineer

Senior Manager, Sales

VP, Finance Control (Korea)

Senior CRA

Senior Designer - Fire Engineer

Technical Support Analyst – Workstation Support Analyst

[Coupang Pay] Director, Back-End Engineering

Client Advisor, Korea

More jobs to discover

11의 software specialization, sr staff에 대한 최신 취업소식을 받고 싶습니다.

더 많은 지역의 채용공고 둘러보기

구직자 도구

기업회원 도구

찾아보기

연결 상태 유지하기