Are you interested in assisting the Study Start Up Team Lead in the development of the plan for country and site distribution and execution of SSU activities in assigned countries?
In this role you will be responsible for performing feasibility, site identification, site contract negotiation, and other SSU activities.
Provide country specific SSU expertise to Study Start Up Team Leads and project teams.
The Sr SSUA will also be responsible for the preparation and coordination of submissions to regulatory, ethics, and other bodies.
Develop, finalize, and review Master and Country Specific Subject Information Sheets / Informed Consent Forms.
We are presently in over 40 countries with over 80 offices worldwide and over 12,500 employees globally. We are comprised of 6 divisions and offer a full-
service portfolio of solutions to our clients.
We provide a Sr Study Start up Associate with the resources to be successful and visibility by having them provide input and recommendation to upper management on the study start up submission process and how to better the work process.
In addition to partnering with the top pharmaceutical and biotech companies in the world we offer a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, bonus plans, vacation, and other incentives.
A Bachelor’s Degree or local equivalent and / or appropriate experience from the Medical / science background and / or discipline.
A minimum of 3 years of experience or understanding of clinical study start up requirements and activities. Fluency in the local language and English is essential.