Senior Clinical Data Associate

Date Posted: Tuesday, 14th of February 2012

Salary: £25,000 - £30,000

Start Date: 12 Mar 2012

Telephone: +44(0)1438 870028

Location: Yorkshire

Consultant Name: Priya Mukherjee

Sector: Clinical

Description

CK Clinical is recruiting for a Senior Clinical Data Analyst who will independently perform all clinical data cleaning activities on assigned projects and commensurate with experience and/or project role. You will be responsible for coordinating a moderate to large team or multiple small size protocols as the CDA Coordinator, with minimal to no supervision. You may also be tasked with the role of a CMA/CDA Coordinator working on smaller projects.

Key Accountabilities
* Assume the ability tomeet the requirements of a CDA I and II with a high degree of proficiency and autonomy
* Act as an independent CDM Coordinator on complex or multiple projects and CMA/CDA Coordinator on smaller projects
* Manage all phases of data management activities from study start up to database close
* Direct team members in daily activities
* Define and monitors metrics and modifies plan accordingly
* Mentor project team members
* If required, facilitate cross functional team meetings both internally and externally
* Actively review and provide feedback on study productivity
* Recognize out of scope activities and communicates to GRO Lead
* Represent function in external client meetings and presentations such as investigator meetings and bid^defenses as required
* Keeps manager(s) informed about work progress and any issues to avoid surprises
* Apply knowledge across multiple projects
* Define study specific processes
* Identify inconsistencies and inefficiencies in processes and recommends solutions

Interested applicants should hold a degree in Life Sciences (OR Equivalent) with proven experience of working as a Data Manager within a Pharmaceutical/CRO/Biotechnology organisation. You will hold excellent interpersonal, verbal and written communication skills, excellent computer skills including but not limited to the knowledge of Clinical Trial/Data
Management Systems, PMED, IVRS, MS-Office products such as Excel, Word, and you will have an awareness of all relevant regulations, including GCP. Furthermore, you will be able to demonstrate the ability to work as part of a team and independently, be able to communicate and work effectively with clients and demonstrate effective time management in order to meet dailymetrics or team objectives.
Experience with solid understanding of clinical trials methodology and terminology.

CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote referenceCL23706 in all correspondence.

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