Clinical Trial Manager - Dublin - Top 20 BioPharma

JOB TITLE
Clinical Trial Manager - Dublin, Ireland

JOB SUMMARY
I am looking for an individual with at least a year of Clinical Trial Management experience based in Dublin. This is a hybrid role that will require you work in office 2 days a week (Dublin Office). This role you would have you responsible for the management and delivery of Paediatric Clinical Trials, across all therapeutic areas, around the world. My client is a global bio-pharmaceutical company that collaborates with CRO's and works throughout the entire clinical development cycle. This is an exciting opportunity to expand your clinical trial expertise within a working environment that ensures great work/life balance, the ability to gain exposure a dynamic, matrix management structure and highly competitive pay rates.

LOCATION
Dublin

RESPONSIBILITIES

* Leading the trial team and be responsible for the complete cycle of trial related activities
* Being responsible for securing trial deliverables
* Ensuring proper documentation, record management, risk assessment and management, trial budgets and up-keeping sponsor engagement and their oversight activities with a concentration on vendor management (including CRO's)

REQUIREMENTS
* Bachelor of Science/ relevant Scientific discipline or RN qualification
* At least 1+ years' experience as a CTM
* Excellent communication skills in English - both written and spoken
* Entitlement to work in Ireland

* Minimum 5 years of Clinical trials experience
* Ability to work independently
* History of proactively hitting targets and achieve larger project goals by anticipating obstacles and assessing risk
* Exceptional communication, decision making and organisational skills
* Knowledge of FDA and/or EMEA Regulations, ICH Guidelines and GCP governing the conduct of clinical trials

BENEFITS
* Excellent Contracting day rate
* Flexible working times
* Contract extension likely

ABOUT i-PHARM CONSULTING

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

www.i-pharmconsulting.com

TO APPLY

If you would like to discuss this vacancy further, please call Recruitment Consultant, Nicole Crowley on +44 (0)20 7551 0728, or email ncrowley@i-pharmconsulting.com. If this particular role is not suitable, Nicole is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

KEY WORDS
CTM / Clinical Trial Manager / Clinical Study Manager / Clinical Project Manager / CRA / CRA I / CRA II / Clinical Research Associate / SCRA / Senior Clinical Research Associate / Senior CRA / Clinical Monitor / Clinical Trials / Phase I / Phase II / Phase III / Phase IV / Good Clinical Practice / GCP / Oncology / CNS / Neurology / North West / Ireland / Leinster / Dublin / South East / Pharma's / Major Pharma's / Sponsor Pharma's / CRO / Contract Research Organisation / Pharmaceutical /Multiple Sponsors / Home Based / Study Start-Up / Feasibility / Site Identification / Site Initiation / Routine Monitoring / Close Out Visits /