Clinical Data Manager - Homebased

Recruiter
Docs International UK Limited
Location
Marlow, UK
Salary
Competitive
Posted
13 Jun 2019
Closes
27 Jun 2019
Ref
1179734154
Contract Type
Permanent
Hours
Full Time
The lead FSP Data Management point of contact for the Sponsor Data Management Operations

Lead regarding all day today activity on a study with key responsibilities for study setup,conduct

close-out tasks,as well as overseeing and coordinating tasks delegated to the supportive DM

study team members.

WorkscloselywiththecorrespondingSponsorDataManagementOperationsLead(DMOL)to

ensureaseamlessdeliveryofDataManagementdeliverablesincludingholdingregularstatus

meetings with DMOL and other SMT team members as appropriate'

Ensures study/team deliverables are executed to expected quality and timelines,provide

technical oversight as needed,and mentors/develops Clinical Data Management teams and other

staffundertheguidanceofManager/Sr.Manager,DataManagementordesignee.

The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

·Relevant Clinical Data management experience.

·Highly computer literate, including strong Microsoft Office skills (Excel, Word, PowerPoint, Project)

·Knowledge of clinical trial database technologies and processes.

·Is accountable and proactive in quality and risk management.

·Ability to liaise successfully with sponsors.

·Excellent written and oral communication skills.

·Excellent accuracy and attentiveness to detail.

·Capability to work within a team environment.

·Capability to manage competing priorities in a changeable environment.

·Capability to handle stressful situations and deadlines.

·Excellent interpersonal skills.

·5 + years Clinical Data Management experience

·Previous experience and proven competence in managing study delivery through full DM lifecycle(planning, start-up, conduct, lock and closeout)

·Thorough knowledge of Data Review Process; E.g. SAE and external vendor data reconciliation, central and local laboratory data review, query writing and management, cross panel consistency checking, etc.)

·Comprehensive understanding of clinical development drug development process

·Proven ability to handle a high volume of highly complex tasks within a given timeline and demonstrate effective prioritization

·Able assess and communicate DM resource requirements

What is required

Bachelordegreeorlocalequivalentinascientificand I orappropriateexperience.

What is offered

•Competitive salary

•Home-based

•Permanent Position

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