Senior Project Manager, CNS - EMEA

Clinical Research Project Manager Opportunities with ICON across Europe

Home based contracts as option

Opportunities at Project Manager and Senior Project Manager levels

Are you an experienced Clinical Research Project Manager with experience in the Pharma or CRO industry sectors managing global, complex clinical research trials?  We have opportunities across Europe in most of our Therapeutic Teams. Those teams with opportunities are below:

Oncology – particular TA experience of interest Oncology and Haematology

Internal Medicine – particular TA experience of interest Gastro-interology, Dermatology, Respiratory and Immunology

CNS – particular experience of interest Alzheimer’s Disease, Parkinson’s Disease, Multiple Sclerosis and Epilepsy

Cardiovascular and Metabolic – particular TA experience of interest here is NASH (non-alcoholic steatohepatitis) or Hepatology in general Diabetes, CVOT (Cardiovascular Outcomes Trials) and Endpoint Trials.

Vaccines and Infectious Diseases – particular interest in Vaccines, Infectious Diseases, Women’s Health and Rare Diseases.

Project Manager role at ICON:

As a Project Manager within our team, you will be expected to contribute towards a culture of business excellence with a focus on streamlining processes, adding value to the business and exceeding client needs.  You will be the primary point of contact for designated projects, responsible for: delivering successful working relationships with clients, cross functional project planning, scheduling and implementation, defining project scope, resource requirements and deliverables, risk migration strategies, associated action plan and issue resolution. 

As Project Manager, you will manage a cross functional project team ensuring all necessary project training is provided and developing a succession plan for the core team members.  Manage projects in accordance with the contract including: study budget, study invoicing procedures, monitoring and reporting on progress of projects to stakeholders and implementing QC activities as necessary. Collaborate with business development to ensure proactive commercial aptitude while partnering with internal and external stakeholders to identify new avenues for growth and also contribute and particulate in Bid Defence Meetings..

Role Requirements:

Bachelor’s Degree in medicine, science or equivalent degree and a qualification in Project Management or equivalent (PMI certification) are desirable. At least 4 years PM experience within clinical research is essential. Specific therapeutic experience in CNS and comprehensive knowledge of ICH-GCP is essential along with excellent communication, planning, decision-making, negotiation, conflict management and time management skills.  Willingness to travel up to 25% as needed.

Benefits of Working in ICON:

ICON provides Project Manager’s with the innovative resources to be successful in delivering results, inspiring others and becoming a trusted partner. We offer an exceptional benefits package that includes a comprehensive health plan, retirement plans, highly competitive pay, corporate bonus plan, time away from work, and many other incentives amongst an opportunity to grow your career within our PMO.

What’s Next?

Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.

ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.*LI

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