Site Contract Specialist I

PSI CRO AG; United States; Remote; USD 60,000 - 80,000; Full time

Job summary

Join a dynamic global company dedicated to improving lives through medical science. As a Site Contract Specialist, you will play a crucial role in facilitating site agreements and budget negotiations, ensuring alignment with activation plans. This position offers the opportunity to work in a collaborative environment where your contributions directly impact the success of clinical trials. With a focus on employee well-being and professional growth, this role is perfect for those looking to make a meaningful difference in the pharmaceutical industry. If you have a passion for research and a commitment to excellence, this is the opportunity for you.

Qualifications

• Degree or equivalent experience required with 2+ years in relevant fields.
• 1+ year experience in clinical research industry in the US.

Responsibilities

• Facilitate negotiations of site agreements and budgets.
• Prepare and customize site-specific agreements and manage translations.
• Track status of site agreement negotiations.

Skills

Negotiation Skills

Knowledge of Medical Terminology

Organizational Skills

Education

College or University Degree

2 Years Relevant Experience

Job description

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2700 driven, dedicated and passionate individuals. We work on the front line of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

The Site Contract Specialist can be based anywhere in the United States.

The core responsibilities of this role include:

• Facilitating negotiations of site agreements and budgets to ensure alignment with the site activation plan
• Customizing and preparing country- and site-specific agreements and organizing their translations
• Tracking the status of site agreement and budget negotiation
• Preparing executable versions of site agreements and budgets, and coordinating the signature process
• Filing executed site agreements in the Trial Master File
• Updating all concerned functions on the site contracting process

Qualifications

• College or university degree or an equivalent combination of education, training, and experience that presents the required knowledge, skills, and abilities. Equivalency is defined as a minimum of 2 years’ experience in an environment, where relevant experience has been gained.
• Minimum 1 year experience in the clinical research industry in the United States
• Knowledge of and experience with legal documents related to clinical trial sites and medical terminology is a plus.

Additional Information
If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.

Seniority level

Associate

Employment type

Full-time

Job function

Research

Industries

Pharmaceutical Manufacturing