Study Start Up Associate Ii

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.

With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

**The Role**:
Study Start Up Associates are integral in ensuring that clinical research sites are prepared and have the necessary tools and approvals needed to start the trial of investigational, new pharmaceutical and biological products for clinical trials.

As a Study Start Up Associate at ICON working in contracts and budgets your main role is to review and negotiate clinical site investigator contracts and budgets. You would maintain communication with Investigative sites, sponsors and internal personnel regarding the status of contracts and contract-related documents, prepare and oversee preparation of contractual documents and correspondence, and facilitate the indemnification process between the study sponsor and the site. Further you would serve as the internal consultant on study budgets with respect to investigator payments, develop and update training documentation and conduct group training as necessary, mentor and train new and junior personnel in the study start up department, and act as consultant on the Investigator Contract and Budget development process from origination through execution.

**To be successful in the role, you will have**:

- A high school diploma or local equivalent
- Bachelor’s Degree preferably in Life Sciences
- Minimum of 1 years’ experience or understanding of clinical study start up requirements and activities.
- We are looking for associates who have experience in a clinical research environment with specific experience in study contracts review and budget negotiation or experience in a related field such as where contract or legal document review was a primary function.

**Benefits of Working in ICON**:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

ICON plc est une organisation de recherche clinique et d’intelligence en soins de santé de premier plan à l’échelle mondiale. De la molécule au médicament, nous faisons progresser la recherche clinique en offrant des services externalisés aux entreprises pharmaceutiques, biotechnologiques et de dispositifs médicaux, ainsi qu’aux organismes gouvernementaux et de santé publique.

En mettant nos patients au centre de toutes nos activités, nous contribuons à accélérer le développement des médicaments et des dispositifs qui sauvent des vies et améliorent la qualité de vie.

Nos collaborateurs sont notre plus grande force, ils sont au cœur de notre culture et la force motrice de notre succès. Les employés d’ICON ont pour mission de réussir et sont passionnés de sorte que ce que nous faisons, nous le faisons bien.

**Description de l’emploi**:
Les associés chargés du lancement des études veillent à ce que les centres de recherche clinique soient préparés et disposent des outils et approbations nécessaires pour lancer l’étude de nouveaux produits pharmaceutiques et biologiques pour les études cliniques.

En tant qu’associé(e) au lancement d’études chez ICON, travaillant dans le domaine des contrats et des budgets, votre rôle principal est d’examiner et de négocier les contrats et les budgets des chercheurs des centres d’études cliniques. Vous maintiendrez la communication avec les centres d’investigation, les commanditaires et le personnel interne en ce qui concerne l’état des contrats et des documents connexes, préparerez et superviserez