Contact

Clinical Professionals

T (UK) -
+44 (0)118 95 94 990

T (EU) -
+44 (0)207 822 1710

T (DE) -
+49 (0)711 222 54 403

T (BE) -
+32 (0)2 892 3993

T (IE) -
+353 (0)144 752 96

E -
apply@clinicalprofessionals.co.uk apply@clinicalprofessionals.eu

Share &
Connect


Keep connected & join the Clinical Professionals Network here.

Clinical Professionals LinkedIn Clinical Professionals Facebook Clinical Professionals Twitter
Clinical Professionals Pinterest Clinical Professionals YouTube Clinical Professionals Google+
Integrated Regulatory Outsourcing German Pharmaceutical Jobs Pharmaceutical Physician Jobs

Reference No: J11871

Clinical Operations Manager - 12 month Contract
Major Biotech based in Cambridge

A market leader, our client strives to develop products that change people's lives and in the last 30 years have transformed the management of anaemia, inflammation, and cancer. They have a thriving pipeline and are currently very active in recruiting candidates to join the team on a contract basis.
Both UK sites are easily reachable by mainline BR and have excellent road links with ample free car parking.

Our client knows they offer a great place to work. Our client understands that each candidate is not the same, and no two roles are either. That's why they permit up to two days working from home per week depending on the role. Moreover, it's a place where you will be more than a contractor- you will be one of the team, and that even means an early Friday finish!

Job Summary
-In this challenging role you will be responsible for local protocol and site feasibility assessments.
-Locally plans, executes, and manages and reports on our clients sponsored studies.
-Manages the feasibility process and ensure adequate site selection
-Plans, manages and executes all client sponsored study related activities within the affiliate
-Ensures the timeliness and quality of study deliverables in accordance with SOPs, ICH/GCP guidelines and local regulations
-Actively contributes to results oriented department goals
-Drives continuous improvement of Global study operations
-Promotes operational and scientific excellence within local Global study operations
-Provides a single point of contact at the study level for LOC

Key Activities
-Manages the feasibility process and ensure adequate site selection
-Plans, manages and executes all our clients sponsored study related activities within the affiliate
-Ensures the timeliness and quality of study deliverables in accordance with SOPs, ICH/GCP guidelines and local regulations
-Coordinates tasks when those are allocated to support COM-managed studies
-Actively contributes to results oriented department goals
-Drives continuous improvement of Global Clinical Study Management (GCSM)
-Promotes operational and scientific excellence within local GCSM

Essential Skills & Qualification
-BA/BS/BSc or qualified nurse (RN)
-Clinical research clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company, or other relevant clinical setting
-Clinical trial management experience
-Operational performance measurement experience
-International collaboration experience.

If this role is of interest to you please contact our expert consultant on the details below:

Catherine Kennedy: 01189594990 / ckennedy@clinicalprofessionals.co.uk

Keywords: Clinical Research, Clinical Operations, Clinical R&D, CRA, CTM, GCP, Manager, Study Manager, EUCTD, ICH GCP, Project Manager, Clinical Study, Clinical Programme, Feasibility , Essential Documents, SOPs, Investigator Meeting, REC, Lead CRA, CRA , Clinical research Associate, Vendor

Apply for this position

We also have other jobs matching this description.


Would you like to view a list of similar vacancies?

Job Search

Advanced job search

Register your C.V.