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Job Details

Senior Clinical Research Associate - UK - Small CRO

Company: Barrington James Clinical
Location: Home Based
Reference: WP29/01CRAUK
Closing Date: 28 Feb 18
Type: Permanent
Salary (£): On Application
Benefits: Great Benefits

Job Summary:

Are you a CRA that needs an opportunity to expand your career? Well this job vacancy could give you that opportunity to do just that. They are a leading CRO in cutting edge and exciting research specialising in Transplantations and rare Orphan diseases. This CRA job allows you to work closely in a well-established professional team with interactions from senior members of the organisation.

Requirements:

Job Vacancy Notice

Position: Clinical Research Associate

Location: England, United Kingdom

Employment Classification: Full-time

Are you a CRA that needs an opportunity to expand your career? Well this job vacancy could give you that opportunity to do just that. They are a leading CRO in cutting edge and exciting research specialising in Transplantations and rare Orphan diseases. This CRA job allows you to work closely in a well-established professional team with interactions from senior members of the organisation. If you have experience in complex indications or oncology trials and want to help save lives apply for this very promising vacancy.

Qualifications/Skills Required:

Minimum of 2 years of clinical nursing experience OR minimum of 1-2 years of experience in related health care or clinical research work (i.e. Study Coordinator) OR minimum of 1 year experience performing relevant project support in-house functions

Previous practical experience in conducting clinical pharmaceutical research studies in a hospital setting, pharmaceutical company or CRO is preferred

Experience or education providing a sound basic knowledge of medical and pharmaceutical terminology

Bachelor’s or Master’s degree in allied health fields, such as nursing, pharmacy, or health/natural science OR RN with Associate’s degree OR 3-year Nursing Diploma OR equivalent combination of education and relevant work experience

Responsibilities:

Serves as a main contact for assigned investigative sites

Manages investigative site activity for multiple protocols/ indications and provides ongoing updates of site status to study manager/ sponsor

Creates and implements subject enrolment strategies for assigned investigative sites

Conducts study site visits (pre-study, initiation, monitoring, and close-out) and completes  site visit deliverables within given timelines in the monitoring plan

Ensures proper storage, dispensation and accountability of all investigational product(s) and trial-related material

Maintains tracking records for assigned sites including tracking of subject status, subject CRF retrieval/ source document review, regulatory documents, and investigational product

Completes in-house monitoring activities as appropriate, such as updating in-house site files, conducting remote monitoring for EDC studies, and completing visit reports/ letters

Anticipates/identifies site issues and implements corrective actions or escalates to study manager/ sponsor as necessary

Completes site selection and pre-study activities to identify and evaluate potential investigators

Participates in study-specific training

Conducts project-specific administrative activities as a member of the project team

Assists in the preparation and coordination of project investigator’s meetings and attends the meetings as necessary

Attends sponsor meetings as necessary

Serves as a mentor/ trainer for CRAs including in-house and on-site training

Participates in the interview process for CRA candidates

Assists with project-specific administrative activities as a member of the Project Team.

Responsible for representation of this company in a professional manner

Increases knowledge of drug development process, therapeutic areas, Good Clinical Practices (GCPs) and any applicable local regulatory requirements

Accurately completes this companies administrative activities in a timely manner

Assists with data entry to the extent such assistance is needed

Interested applicants should forward their CV/Resume to:

Name:                          William Penticost

Position Title:             Recruitment Resourcer

Company Name:        Barrington James Ltd

Phone Number:          01293 776644

Email:                           wpenticost@Barringtonjames.com

Apply for this job: Senior Clinical Research Associate - UK - Small CRO

Contact Information:

Address:  Head Office
Victoria House Consort Way Horley Surrey
RH6 7AF
England
Tel:  01293 776644
Fax:  01293 822333
Website:  Visit Our Web Site

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