sops coordinator
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Clinical Trial Services company, currently undergoing a period of major expansion, seek a motivated and enthusiastic CRA for a new department. Working directly with experienced Clinical Trial Physicians, your role will be to work with site staff to ensure correct procedure is being followed. A strong understanding of GCP and SOPs is required, as are a real eye for detail..., Clinical Trials, GCP, SOPs, Contract, England, North West
Experience: N/A
Contract: Temporary/Locum
13 hours, 16 minutes ago in jobs4dd Save
Barrington James are looking for an experienced Study Site Coordinator to coordinate, organise and control all of the... of the Study Site Coordinator are: ⢠To act as Study Site Coordinator on Clinical studies. ⢠To supervise and assist in..., SOPs and within regulatory timelines. ⢠To ensure the preparation of source document forms and any specialist forms and... adhere to, Standard Operating Procedures (SOPs), legal and regulatory requirements including ICH Good Clinical Practice (GCP...
Experience: 2 years
Contract: Permanent
6 days, 13 hours ago in jobs4dd Save
Clinical Research - CRA, Clinical Study Coordinator
Any Location
Salary: Negotiable (24000 - 32000 £)
As a Clinical Research Associate, you will become a member of a highly regarded clinical study team and will be primarily responsible for providing essential monitoring support. The successful candidate will ensure that the trial is conducted, recorded and reported as stated in the protocol, SOPs and GCP. It is essential that you hold a degree in a scientific or healthcare discipline and have demonstrable experience in phase II and III studies. You will have excellent communication skills and...
Experience: 1 years
Contract: Permanent
6 days, 13 hours ago in jobs4dd Save
* DEPARTMENT: Data Management JOB TITLE: Clinical Data Coordinator III REPORTS TO: Appropriate Data Management manager A. PURPOSE... Procedures (SOPs), Working Procedures (WPs), Study Specific Procedures (SSPs), International Committee on Harmonization (ICH... binders in accordance with SOPs. ⢠Perform other project activities as required in order to ensure that study timelines... Coordinators in data management requirements and activities, including adherence to GCPs, ICON SOPs, WPs, SSPs, ICH Guidelines and...
Experience: 3 years
Contract: Permanent
13 hours, 16 minutes ago in jobs4dd Save
To monitor investigator sites in compliance with Company SOPs and ICHGCP, so that recruitment targets are achieved and that... ICHGCP and Pfizer SOPs and procedures Quality of data collected. Time to issue' resolution Standard of study documents...
Experience: 1 years
Contract: Temporary/Locum
1 day, 13 hours ago in jobs4dd Save
meet and use your experience to make it possible to exceed the set study timelines. Required skills and abilities: - Knowledge of drug development process - Knowledge of applicable regulatory requirements, SOPs, and companyâs Corporate Standards...
Experience: 3 years
Contract: Permanent
6 days, 13 hours ago in jobs4dd Save
Clinical Research - Clinical Study Coordinator, Clinical Study Admin
Hertfordshire
Salary: Negotiable (50000 - 65000 £)
, clinical operating guidelines and standard operating procedures Monitor and review incoming data and ensure that the SOPs for evaluating, documenting and reporting adverse events are strictly followed. Prepare annual reports and safety updates Provide...
Experience: N/A
Contract: Permanent
1 day, 13 hours ago in jobs4dd Save
Clinical Research - CRA, Clinical Study Coordinator, Clinical Trial Administrator
Berkshire
Salary: Negotiable
accordance with SOPs, applicable regulations and the principles of ICH âGCP The minimum experience required is a life science degree with one years monitoring experience; MUST be monitoring clinical trials. If you feel you have the passion and desire...
Experience: 2 years
Contract: Temporary/Locum
6 days, 13 hours ago in jobs4dd Save
Clinical Research - Clinical Study Coordinator, Clinical Study Admin, Clinical Trial Administrator
Buckinghamshire
Salary: Negotiable
with the will to succeed. You will be involved in most activities of the clinical trial required to set-up, conduct and complete ensuring you work to ICH GCP and company SOPs, including, but not limited to: ï§ Assist in the preparation of documentation...
Experience: N/A
Contract: Permanent
3 days, 13 hours ago in jobs4dd Save
Clinical Research - Clinical Study Coordinator, Clinical Study Admin, Clinical Trial Administrator
Buckinghamshire
Salary: Negotiable
with the will to succeed. You will be involved in most activities of the clinical trial required to set-up, conduct and complete ensuring you work to ICH GCP and company SOPs, including, but not limited to: ï§Assist in the preparation of documentation...
Experience: N/A
Contract: Permanent
3 days, 13 hours ago in jobs4dd Save