Associate Clinical Research Coordinator

Identify, select, initiate, and close-out appropriate investigational sites for clinical studies. Monitor those sites in order to ensure that studies are carried out according to the study protocol, ICON SOPs/WPs, applicable regulations and the principles of ICH-GCP Depending upon experience, become involved, when required, in other areas of study management...

Roles & ResponsibilitiesThe Associate Clinical Research Coordinator (ACRC) shall assist all levels of Clinical Research Coordinators (CRCs and above), in coordinating clinical research.The ACRC has to ensure that trial- related work is conducted and recorded in accordance with the protocol, Good Clinical Practice (GCP) Guidelines, all applicable regulatory...

SingHealth PolyclinicsClinical Research Coordinator (Contract): Job Category: AdministrationPosting Date: 9 Feb 2024You will assist Principal investigators in conducting clinical trials & research projects according to Singapore Good Clinical Practice (GCP) guidelines. You will plan, organise & coordinate workflow of study projects from initiation to...

Responsibilities: Provide research support service to Associate CRC for clinical trials/research in accordance to ICH-GCP and protocol requirements Managing/Assisting in conducting trial procedures, administer quality of life questionnaires or other types of surveys Managing/Assisting in collecting, processing, labelling and storage of biological samples and...

Are you a passionate professional and proactive individual who is looking to build a career in clinical research?Aesculape CRO is expanding and we have an outstanding offer for youWe are a Clinical Research Organization based in Belgium with presence in Asia, and we are looking for an experienced full time Clinical Research Associate to join our APAC team in...

Roles & ResponsibilitiesThe Associate Research Coordinator (ARC) will work with the Principal Investigator (PI) and Department of Breast Surgery to support administration of the compliance, financial and various operational aspects of clinical studies.Responsibilities: Assist in all aspects of study operations for clinical studies. Take patient consent in...

Roles & ResponsibilitiesAs a clinical research coordinator, you will be actively involved in coordinating clinical trial activities according to the study protocol and in compliance to the ICH Good Clinical Practice guidelines and the Health Products (Therapeutic Products) Regulations under the Health Product Act.You will support and assist the Principal...

Family Group: Allied HealthStatement of PurposeTo facilitate clinical research activities in the hospitalMAJOR DUTIES AND RESPONSIBILITIES Liaison person with Principle Investigator (PI), sitePI and various departments for clinical research procedures e.g. Specialist Clinics, Laboratory, wards, etc. Plan, organise and coordinate the workflow of the research...

Liaison person with Principle Investigator (PI), site-PI and various departments for clinical research procedures e.g. Specialist Clinics, Laboratory, wards, etc. Plan, organise and coordinate the workflow of the research study Adhere to protocol procedure Screen research participants for eligibility according to research protocol Enrol research participants...

Roles & ResponsibilitiesJob DescriptionSupport the investigators in implementing clinical trials protocols: Liaise with the study site personal to implement the study per global and local requirements. Ensure compliance with all ethical, regulatory and contractual requirements. Training of study site personal (protocol, use of IP, SOPs, etc.). Ensuring data...

Responsibilities: Coordinate and conduct clinical research studies Assist in the development of research project Conduct literature search and write up Enter and manage data collection Involve in preparation of posters and presentation to the publicJob Requirements: Degree in the relevant discipline or one with relevant working experience Preferably with 12...

Roles & ResponsibilitiesResponsibilities: Assist in the planning and execution of clinical research studies. Coordinate and oversee the collection, analysis, and interpretation of study data. Ensure compliance with study protocols, regulatory requirements, and ethical standards. Conduct site visits to monitor study progress and ensure adherence to study...

Clinical Research Coordinator, Healthcare RedesignThe hospital is a test bed for innovative care approaches in Singapore and is currently running a diverse portfolio of studies.The research assistant will assist in the coordination and the conduct of clinical research studies and trials in NUHS in compliance with study protocols, guidelines, policies and...

Roles & ResponsibilitiesJob Description:A clinical research coordinator will assist Principal Investigator or Co-investigators to monitor the administration and progress of a clinical trial.You will be responsible for the following research activities at NUH:· Oversee overall clinical operations related to the conduct of the clinical trials.· To adhere to...

As our business grows, we are looking to further strengthen our Clinical Operations team in IQVIA Pakistan. We have a number of great opportunities for Clinical Research Associate and Senior Clinical Research Associate in Karachi, Lahore, and Islamabad.You will perform monitoring and site management work to ensure that sites are conducting the study(ies) and...

Roles & ResponsibilitiesJob Purpose A clinical research coordinator will assist Principal Investigator or Co-investigators to monitor the administration and progress of a clinical trial.Duties and ResponsibilitiesPrimary Duties and ResponsibilitiesClinical Trial Oversee overall clinical operations related to the conduct of the clinical trials. To adhere...

KK Women's and Children's Hospital PteLtdClinical Coordinator: Job Category: Allied Health ProfessionalPosting Date: 31 Mar 2024Clinical CoordinatorThe Clinical Coordinator will provide overall clinical (direct and indirect patient work), research and administrative support for the Children's Cancer Foundation (CCF) Psychosocial and Supportive Care...

Roles & ResponsibilitiesThe Clinical Research Coordinator (CRC) shall help investigators conduct mainly investigator-initiated clinical trials. The CRC has to ensure that clinical trials are conducted and recorded in accordance with the protocol, Good Clinical Practice (GCP) Guidelines, all applicable regulatory requirements and the Clinical Trials...

Job Description:You will be responsible for the following:a) To adhere to compliance with Research Governance, Good Clinical Practice, Data Protection and Ethical Requirements.b) To ensure the study and study procedures are conducted in accordance with the study protocol.c) To participate in patient recruitment.d) To ensure informed consent procedure is...

Singapore General Hospital Pte LtdResearch Associate:Job Category: Allied Health Professional- Posting Date: 25 Jan 2024Job Responsibilities Performing analysis of data and ensuring data quality and integrity: coding, evaluating and interpreting collected data and preparing appropriate documentation Developing and maintaining hardware and software systems...