Clinical Professionals Ltd

CTA

Location
Leeds
Salary
Competitive
Posted
13 Dec 2018
Closes
14 Feb 2019
Ref
JO-1812-421276
Contract Type
Contract

CTA / Clinical Trials Administrator

Our client, a large Global Medical Device with Offices across the EU and America, are seeking a CTAs from all levels.
Due to continued expansion they have created a new position for a CTA / Clinical Trial Administrator to work from their UK office in Leeds.

Job title:
CTA / Clinical Trial Administrator

Location:
Leeds suitable for someone residing in Leeds, South Yorkshire, Yorkshire, Bradford, Oakwood, Boston Spa, Horsforth, Rothwell, Swillington
Salary: To be discussed via telephone conversation

Key Job Activities:
Clinical Administration Tasks - (includes CTMS build and tracking, v-TMF build & upload)
Under general supervision, accountable for the timely tracking of study essential documents and ensuring completeness of the Trial Master File for assigned clinical studies according to appropriate regulations, departmental guidelines, and work instructions.
Creation/distribution of regulatory binders & the wet-ink signed documents binder
Assist study staff and investigators to quickly and effectively resolve issues relating to Study Files (Trial Master File and Investigator Site File). Respond to problems and assists in implementing corrective and preventive actions.
Assist in providing internal communication of important clinical data and events.
Support ongoing use of CTMS by maintaining and tracking relevant activities.
Provide safety documentation to other functional groups in support of safety committee meetings as requested (supporting role).

Other Administrative Tasks:
May be asked to provide support for study supplies creation, ordering and distribution to the sites e.g. print protocols, burn DVDs
May be asked to assist with Device tracking and ordering if required and if applicable.
Assistance with logistics for Investigator meetings/expert panel meetings
Assistance with distribution of newsletter (create mailing list from CTMS and routing for internal approval)
Participates in process improvement activities related to CTMS/v-TMF within the department.
Job Qualifications

Summary:
This is an excellent opportunity to join a market leading Device company company with a strong pipeline of products. They offer stable and progressive careers, excellent training and support.

Please apply today or contact Luke Morrisen within the Clinical Team for more information. luke@clinicalprofessionals.co.uk / 01189 594 990

Clinical Professionals is the leading pharmaceutical staffing consultancy in Europe. Our dedicated Clinical Team has over 10 years experience of placing clinical research professionals into positions within Pharmaceutical, Biotech, CRO, Charity and Academia organisations. We work with global market leaders as well as partnering with SMEs and Start-ups. If you are on the market for a new challenge, please contact the team today.

Similar jobs

Similar jobs