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Project Manager, Data Management

hace 3 semanas

Desde casa, Colombia ICON A tiempo completo

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.

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.

We have an incredible opportunity for a **Project Manager**, Data Management** to join the team.

**Location**:home-based OR office-based
- Canada
- Mexico
- Colombia

**Overview of the role**:
The Project Manager, Data Management will be responsible for the management of data teams, studies, and programs of studies. This will include providing planning estimates for project scope, schedule and resource requirements ensuring programs are properly budgeted, estimated and scheduled. This person will work closely with other departments to ensure all data collected during trials is managed and meets regulatory guidelines.
- Oversee the day-to-day activities and task management of the project team to ensure that a focus on quality, budget, and timelines on each project is reached and maintained
- Lead and motivate a team according to organizational goals
- Plan, implement, and deliver the project in accordance with the contract agreed with the sponsor
- Prepare and manage the overall project budget throughout the life cycle of the project, taking overall responsibility for cost control, timelines, and project quality
- Typically responsible for handling multiple studies running concurrently
- Deliver project to quality, timeline, and budget requirements
- Negotiate with clients and/or external customers/departments in relations to timelines and key deliverables
- Research and recommend new data management processes, which address customer needs and key business objectives

**To be successful you will need**:

- 6+ years of clinical data management experience, including experience preparing and managing project budgets (preferably in a Clinical Research Organization or pharmaceutical company)
- 3+ years of experience leading studies with key responsibilities for study set-up and close-out tasks
- Experience with at least one of ICON’s preferred CDMS (e.g. Rave, Inform, Oracle Clinical, OCRDC, UX EDC)
- Highly computer literate, including strong Microsoft Office skills
- Excellent communication and interpersonal skills
- Strong client relationship management skills
- Excellent organizational and planning skills as well as a demonstrated aptitude for project management

**Benefits of Working in ICON**:
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.**

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