Study Start-Up Project Manager - 6 Months Contract

ROLE/DESCRIPTION

As a Clinical Project Manager in Study Start Up you will be expected to undertake full lifecycle and cross functional responsibilities which will include:

* Provides oversight of all the project study start up activities: site selection to site activation-ready.
* Responsibility for study start up deliverables at the project level following the project requirements and the applicable plans.
* Act as the primary global liaison during Study start up
* Assisting in the management of multifunctional leads associated with Study start up.
* Site selection, site set up, clinical trial regulatory works such as reg submissions, communication to the relevant authorities/ethics committees import licences, study maintenance submissions.
* Essential document collection leading to site activation, Site contract management; and overall timeline management

REQUIREMENTS

* A Life Science or Nursing Degree
* Experience in clinical research, including previous CRA and Project Management Experience, study start up experience is also ideal.
* Experience in CRO sector is desirable
* Strong communication and interpersonal skills, including good command of English language
* In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and ICH guidelines

KEYWORDS: CLINICAL PROJECT MANAGER, START UP, START-UP, PROJECT MANAGER, STUDY MANAGER, CLINICAL, PROJECT, PHASE I-IV, PI-IV

To find out more about Real Staffing please visit www.realstaffing.com