Clinical Trials Jobs in Seoul
Clinical Trials Jobs in Seoul
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As Clinical Trials Data Coordinator/Data Manager you will work in close partnership with the GHTU team in close communication with Chief/Principal Investigators and will be responsible for all aspects of the data management process including development of project documentation databa More...
As Clinical Trials Data Coordinator/Data Manager you will work in close partnership with the GHTU team in close communication with Chief/Principal Investigators and will be responsible for all aspects of the data management process including development of project documentation databa More...
As Clinical Trials Data Coordinator/Data Manager you will work in close partnership with the GHTU team in close communication with Chief/Principal Investigators and will be responsible for all aspects of the data management process including development of project documentation databa More...
As Clinical Trials Data Coordinator/Data Manager you will work in close partnership with the GHTU team in close communication with Chief/Principal Investigators and will be responsible for all aspects of the data management process including development of project documentation databa More...
Ociate Manager Clinical Trials Regulatory Management Mwd
This a Full Remote job, the offer is available from: Africa, EMEA Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTR More...
Location: Berlin Hamburg or UK We are currently seeking a highly motivated Project Manager (m/f/d) to join our team. In this role you will be responsible for overseeing and leading international patient recruitment projects (30 countries) from start to finish ensuring adherence to qu More...
Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex Ability to administratively and technically/scientifically review core scientific documentation and feedback gap analysis to customers. Prepares and maintains core clinical trial submission More...
Day to Day: This opportunity will be part of the clinical trials in a pharmacy. Bringing the trials to the people at their local pharmacy. The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruitin More...
Job Title: Clinical Research Coordinator Location: St. Paul MN 55102 Schedule: Business hours Monday through Friday (40 hours per week with potential overtime as needed) Position Type: 6month temporary position with possibility of extension Job Description: The Clinical Research Coor More...
Our Client Our client is a leading Clinical Research Organization (CRO) dedicated to improving global health by providing highquality clinical research services. The team of experts collaborates with pharmaceutical biotechnology and medical device companies to design manage and analy More...
DescriptionSenior Clinical Research AssociateManage and monitor the progress of clinical studies at investigative sites or remotely and ensure clinical trials are conducted recorded and reported in accordance with the protocol standard operating procedures (SOPs) ICH/GCP and all appli More...
Sas Developer With Clinical Domain Experience - Hybrid
Looking for Candidates near to Chicago IL who can go onsite.SAS Developer with clinical domain experienceChicago IL Onsite ( hybrid )Must have overall 10 years ExpShould have at least 78 years of experience in Clinical domain along with clinical trials reporting experience Looking f More...
Location : IC: NIDDK Street: 10 Center Dr Bldg.: NIHBC 10 Clinical Center Room: 9C432A City: Bethesda State & Zip: MD 20892 Weekly Hours FT: 3040 hours per week Total No. of Hours : 40 Overall Position Summary and Objectives Supports the operation of clinical trials. Min Educ More...
Accountabilities: As a Clinical Programmer II, you will design, develop, implement, and validate programs created in SAS/Python/R/SQL or dashboard applications such as PowerBI/Spotfire/MicroStrategy. You will process, analyze and report clinical trial data for review by clinical More...
Responsibilities Provide strategic leadership and operational oversight to the Global Clinical Operations team. Develop and implement standard operating procedures (SOPs) in line with regulatory compliance requirements, Good Laboratory Practice (GLP), Good Clinical Practice (GC More...
Typical Accountabilities Responsible for implementing aligned vendor management and alliance strategy. Identify potential space for improvement and implementation excellence, accelerate strategy implementation and maximize value creation to clinical trial delivery. Manage routin More...
. Defines the clinical strategy, milestones and resources required to meet development decision points/Target Product Profile TPP), Target Product claims (TPC) and target labeling . Permanent member of the Project Core Team, representing Global Clinical Development. . Leads/chairs t More...
Medical Director Clinical Lead Dermatology
. Provides guidance to Clinical Study Teams to ensure alignment of clinical trials planning and conduct with the overall development strategy. . Review and approves (when applicable) key clinical trial documents (e.g. protocol, SAP, CSR). . Single point accountable leader for the de More...
On behalf of our client SAKK Kompetenzzentrum we are looking for a Associate Clinical Project Developer Temporary 12 months.The Swiss Group for Clinical Cancer Research employs 70 coworkers at the SAKK Competence Center in Bern. We are a nonprofit organization conducting clinical tria More...
We are looking for an enthusiastic and experienced person to join the Centre for Cardiovascular Science as a Clinical Study Manager to support and deliver cardiology clinical studies within Professor Mills research group. The post holder will have the leading role in planning coordina More...
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