Ref #: 33145

Employment type: Permanent - Full-Time

Location: UK

Description

At ICON Clinical, within our Global Strategic Solutions Team, as part of a large global Clinical Data Management FSP Partnership with a well known global Biotech company, we are currently recruiting for a number of experienced Senior CDM to join us in UK or Ireland, in the roles of Lead CDM / Trial DM.

Title: Senior Clinical Data Manager / Lead Clinical Data Manager / Trial Data Manager
Duration: Full Time Permanent Employment
Location: Home Based in UK or Ireland

Key Requirements and Responsibilities

• As a Trial DM, act as a single point of contact for the study for DM activities.
• Responsible for managing trial level project plans, project risks and mitigations.
• Involved in authoring database specifications, data management plans (DMPs) & data review plans; performs UAT for the clinical databases.
• Manages and Oversees DMs for all study related DM activities (including but not limited to clinical DB set-up, study maintenance activities- inclusive of all clinical data cleaning, and Clinical Database Lock);
• Ensure that all relevant DM documentation is filed in the eTMF for the trials assigned to them.
• Supports External Data Acquisition Specification development with Vendor and Clinical programmer; also, support eCOA implementation.

Requirements:
• 5+ years of DM experience gained within CRO or Pharmaceutical companies with prior experience in trial level DM activities (Study Lead).
• Bachelor’s degree in a related field or equivalent experience.

To learn more or apply, please get in contact with Pradeep Garepalli at DOCS Global.

Please note we can consider only those applicants that are currently based in UK or Ireland ideally (or in Europe) and have existing work rights to work in UK or Ireland. We can not support with Visa / Work Permit sponsorship processes or relocations.

#DMJobs

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.