• Study Start Up Manager Jobs in United States Of America

  • United States Of America, Usa

Job Description:

Study Start Up Manager

US-North Carolina-Raleigh, ICR; US-Tennessee-Brentwood


Reference 060639_2


Are you a driven change manager with a demonstrated track record of leading by influencing and process improvement with clinical trial experience within a global environment ideally with a focus in Study Start Up We are looking for a transformative leader who is focused on process improvement and innovation This role is home -based and can be located anywhere in the US

Manager Study Start up - Contracts and Budgets

The Senior / Manager Study Start will be the Study Start up transformation leader, focused in process improvement and innovation You would work as a resource for and process and global changes, leading training, and global roll outs Providing metrics to key stakeholders, managing regional change requirements as new regulations come on board You will use your project management skills to lead transformation projects within Study Start Up like developing project plans, providing metrics and milestone updates, leading project meetings, and collaborating across functions regarding training, feasibility, and patient recruitment You would be part of a group that influences the resource pool for global process change regarding site activation and global rollouts, providing metrics and dashboards, and managing regional change requirements regarding new regulations

To succeed you will need

We encourage you to apply if you have a been working within the Pharmaceutical industry and are a transformation leader focused on process improvement In addition we are requiring at least two years of global CRO or pharmaceutical experience from a leading organization Key attributes are change management, process improvement, project management, and demonstrated skills to lead by influencing Study start up experience and lean six sigma certification are desirable A minimum education requirement of a Life Sciences Bachelor degree (or equivalent) is required We invite you to review our opportunities at wwwiconplccom/careers

Benefits of working at ICON

ICON offers an exceptional benefits package that includes a comprehensive health plan, retirement plans, highly competitive pay, corporate bonus plan, time away from work, and other incentives You will work with a highly motivated, collaborative team where you will get visibility within the organization You will gain the opportunity to work with clients and influence on the roadmap of initiatives

ICON is a global, top five clinical research organization known for our technological advances and innovative approach to drug development ICON is presently in over 40 countries with over 80 offices worldwide and over 12,000 employees globally We distinguish ourselves by bringing better drugs to market faster in a more cost effective way To do so, we are creating new ways of doing business, managing clinical trials, and rolling out new technologies in the clinical trial business At the end of the day, you will have the satisfaction that we work for our human patients and that you contribute to the well-being of people across the world

Whats 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

Profile Summary:

Employment Type : Full Time
Eligibility : Any Graduate
Industry : Healthcare, Biotechnology/Pharmaceutical/Medicine
Functional Area : Bio Tech/R&D/Scientist
Role : Clinical Research
Salary : As per Industry Standards
Deadline : 18th Mar 2020

Key Skills:

Company Profile:


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