Clinical Research  - Pharmaceutical Jobs Listings in UK

Find a good job in clinical research?
To strengthen our team we are looking for a new worker

Requirements:
- At least 2 years experience as a Clinical Research Associate essential
- Good communication skills
- Independent work, recognition of priorities, forward planning and implementation
- Administrative skills
- Team capacity
- English written and spoken
- Good PC knowledge ...more info>>

Clinical trials (CRA)
Degree: University

Job Description
We are looking for two staff members for the planning, implementation and monitoring of clinical trials. The incorporation of long-term connection with work done by company.

Requirements:
1) Universitäts-Absolventen/innen Diplom-Biologen/innen with / without experience in the conduct of clinical trials
2) Possibly. and other natura...

Roles and Responsibilities
To provide assistance, where directed by the Project Manager, in specific tasks relating to the preparation of the project (e.g. preparation of protocols; icf, preparation of planning documents).
To maintain awareness of local regulatory requirements, and to conduct studies in accordance with SOPs, guidelines and ICH Good Clinical Practice guidelines.
To make regular contact with inv...

Roles and Responsibilities
To provide assistance, where directed by the Project Manager, in specific tasks relating to the preparation of the project (e.g. preparation of protocols; icf, preparation of planning documents).
To maintain awareness of local regulatory requirements, and to conduct studies in accordance with SOPs, guidelines and ICH Good Clinical Practice guidelines.
To make regular contact with inv...

Roles and Responsibilities
To provide assistance, where directed by the Project Manager, in specific tasks relating to the preparation of the project (e.g. preparation of protocols; icf, preparation of planning documents).
To maintain awareness of local regulatory requirements, and to conduct studies in accordance with SOPs, guidelines and ICH Good Clinical Practice guidelines.
To make regular contact with inv...

Roles and Responsibilities
To maintain awareness of local regulatory requirements, and to conduct studies in accordance with SOPs, guidelines and ICH Good Clinical Practice guidelines
To provide assistance, where directed by the Project Manager, in specific tasks relating to the preparation of national and international projects
Co-ordination of CRAs and individual steps of national or multinational multicentr...

Roles and Responsibilities
To maintain awareness of local regulatory requirements, and to conduct studies in accordance with SOPs, guidelines and ICH Good Clinical Practice guidelines
To provide assistance, where directed by the Project Manager, in specific tasks relating to the preparation of national and international projects
Co-ordination of CRAs and individual steps of national or multinational multicentr...

Roles and Responsibilities
To maintain awareness of local regulatory requirements, and to conduct studies in accordance with SOPs, guidelines and ICH Good Clinical Practice guidelines
To provide assistance, where directed by the Project Manager, in specific tasks relating to the preparation of national and international projects
Co-ordination of CRAs and individual steps of national or multinational multicentr...

According to ICH-GCP requirements, the organization responsible for drug clinical trials, implementation, implementation and clinical audit
* According to research programs and project plans to ensure the operation of the implementation of high quality clinical project
* Responsible for organizing the meeting clinical trial investigators, and research units to maintain good communication and coordination
* A...

Description:
Responsible for the organization, coordination, administrative management and monitoring of clinical trials (phase II-III) according to ICH-GCP
Data review and source data verification
Being the main contact person for project management and CRAs
Guiding and supervising CRAs I and CRAs II in order to coach and train them on the job
Ensure investigator compliance with protocol, study proced...

Description:
Responsible for the organization, coordination, administrative management and monitoring of clinical trials (phase I-IV) according to ICH-GCP
Data review and source data verification
Ensure investigator compliance with protocol, study procedures and timelines
Timely resolution of data queries.
Profile:
(Para) medical or scientific education (pharmacy, biology, biomedical sciences, ...)...

Description:
Responsible for the organization, coordination, administrative management and monitoring of clinical trials (phase I-IV) according to ICH-GCP
Data review and source data verification
Ensure investigator compliance with protocol, study procedures and timelines
Timely resolution of data queries.
Profile:
Medical or scientific education (pharmacy, biology, biomedical sciences, ...)
2-...

Description:
Assisting in the administration of safety reporting: Serious Adverse Events and Unexpected Serious Adverse Drug Reaction reporting in order to ensure timely response to safety issues
Providing on-site support for delegated CRA tasks by performing i.e. drug accountability, Investigator’s File completion and collection of Case Report Forms
Assisting in the administration of safety reporting: Serious...

Description:
Responsible for the organization, coordination, administrative management and monitoring of clinical investigations for medical devices
Data review and source data verification
Ensure investigator compliance with protocol, study procedures and timelines
Timely resolution of data queries
Profile:
University degree in sciences, medical or paramedical degree or similar education
Minim...

Description:
Responsible for the organization, coordination, administrative management and monitoring of clinical trials (phase I-IV) according to ICH-GCP
Data review and source data verification
Ensure investigator compliance with protocol, study procedures and timelines
Timely resolution of data queries
Profile:
University degree in sciences, medical or paramedical degree or similar education ...more info>>