March 20, 2018
JOB ORDER NUMBER:
Our client is a full-service clinical research organization (CRO), providing full range of Phase I to IV clinical development services for the world’s leading pharmaceutical, biotech and medical device companies. Our client offers CRO services across multiple therapeutic areas with a solid commitment to overall excellence in clinical trial management. Due to growth of the company, they are seeking to add a GTA-based Project Manager to oversee multiple, global and domestic projects.
This role is suitable for a Project Manager who has worked cross functionally and ideally managed national or global studies in a CRO environment. This role offers a stable career path with opportunities for advancement and mentorship by industry experts. You will be responsible for ensuring that all project deliverables meet the customer/contract expectations. As Project Manager, you will serves as the key operational interface between the firm and their clients. In addition, you will be responsible for the execution of all PM tasks, tactical management and leadership to project teams to ensure client projects proceeds on time, within budget and with quality. If you are looking to partner with a leading organization who takes pride in their employees' work/life balance and their low staff turnover, this is the ultimate role for you.
EXPERIENCE: In order to be COMPETITIVE for this position, you will have:
Preference will be given to candidates with clear demonstration of:
-A minimum 5 years’ Project Management experience.
-Solid industry experience, preferably in a CRO.
-Multi-center experience is a MUST.
-Demonstration of overall coordination and management of clinical trials from start up through close out activities.
-Knowledge of the key principles of cross functional project management (Time, Quality, Cost).
-Thorough knowledge of regulatory requirements, drug development, and clinical monitoring procedures.
-Demonstrated proficiency with ICH/GCP guidelines and regulatory guidelines TPD, EMEA, FDA.
A very attractive and competitive compensation offered commensurate with experience.
B.Sc in Life Sciences
Pari Nejatie, Healthcare Recruitment Consultant
HOW TO APPLY:
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LEARN MORE ABOUT THE RECRUITER:
Pari Nejatie: http://stoakley.com/meet-pari-nejatie/
CRO, Contract Research Organization, clinical trials, Phase 1, Phase 2, Phase 3, Phase 4, pharmaceutical, biotech, clinical research, regulatory requirements, drug development, clinical monitoring, International Conference on Harmonization, ICH, Good Clinical Practice, GCP, Standard Operating Procedures, SOP, TPD, EMEA, FDA, Project Management, PM.
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