Data Project Manager, Full-time, Office Based, Berkshire
A renowned and very personable clinical research organisation who started operations in 1994 with the premise of delivering cost-effective, quick-to-market clinical services^in the emerging markets of Central and Eastern Europe. Since then, an expansion of services to more than 40 countries, including: North America, Western Europe, Central & Eastern Europe, Latin America, India, and South Africa.
As Data Project Manager you will be responsible for all data deliveries for assigned projects within time and budget with highest priority applied to data quality. Responsibility for the planning, organization, and coordination of Data Management & Systems, Statistics and Medical Writing activities in a set of projects belonging to one or more clients; such that quality, timelines and budget meet expectations, will also fall within your remit.
You will also be responsible for developing and maintaining Data Services Plan (DSP) to manage and meet client expectations, and be responsible for overall database consistency across all client studies within a set of projects; manages all activities centered around development and maintenance of Data^Management Plan(DMP) of CRF design, data collection, data retrieval, coding, and query management, generation and release of TLG, and generation and release of CSR for assigned projects. You will oversee, monitor and evaluate all interactions with third party vendors; and ensures data management standards and quality are maintained and implemented across studies.
Essential Skills & Qualification
MS; BS/RN in life sciences
3 to 5 years (MS) pharmaceutical/data management / life sciences or related area
7 to 9 years (BS/RN) pharmaceutical/data management / life sciences or related area
Project management experience
Strong Data Systems (EDC/RDBMS) Experience
Good oral and written communication skills.
Proficient in Microsoft Office Suite including Word, Excel, and Project
Excellent problem solving, analytical, organisational and time management skills
Demonstrates initiative and leadership
Flexible, works well in a team environment
Demonstrates interpersonal and negotiation skills
Demonstrates excellent knowledge of clinical data flow and research design
Clinical database administration and data / system validation experience.
Demonstrates competence with GCP / regional^regulatory guidelines, SOPs (including WPs), medical terminology, standard coding dictionaries, and demonstrates proficiency in applying them to all relevant therapeutic areas
Client management experience
Software Competence: MS Office, MS Project, DOCUMENTUM
Valid Driving License: Essential/Not Required
Working Language(s): English
Requirement for Business Travel: No
Flexible Working Hours: Yes
Hours: Full time
Location: UK; Location Independent, Office Based access near e.g. M3/M4
Plan Start Date: 30th September 2012, Please do not apply if you are unable to meet this start date.
Contract Benefits: Day Rate inclusive of benefits
Company Pension, Life Insurance, Private Healthcare,
Data Manager, Coding, Clintrial, Oracle, SAS, Clinical Study Report, CSR, EDC, MEDRA
Assigned Consultant:Sue Spice at CSL Recruitment on 01932 228928 firstname.lastname@example.org
Please feel free to call for a detailed Job Description or additional information
Applications are reviewed within 24hrs; applicants will only receive feedback if they demonstrate the skills the role requires in their application. The role may be remarketed; if you applied for this role previously and were unsuccessful you will not receive a response. We request that non EU Nationals include evidence of right to work in the country concerned with their application to^be considered. Do supply supplementary information on required location, notice period and expected salary/day rate if you are a new candidate.