PRN Clinical Research Coordinator

Requisition Number: 4413

Position Title: PRN Clinical Research Coordinator 1

External Description:

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of almost 2,500 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

What you will do

The PRN Clinical Research Coordinator 1 is responsible for assuring that the integrity and quality of the Clinical Research trial is maintained and that the trial is conducted in accordance with Good Clinical Practice guidelines and ICH guidelines as applicable.

• Coordinates the trial from phone screening through study completion.
• Perform ongoing communications with the Senior Manager, Study Conduct, Project Manager and the Principal Investigator to ensure that timelines of assigned projects are met and that the integrity and quality of the clinical trial is maintained.
• Serve as the primary contact for the study subjects, as well as site staff.
• Document and maintain records of all oral communications with the Sponsor’s representative in the Study Master File.
• Schedules medical coverage for physicals, dosing, etc.
• Assures quality and completeness of source documents and Case Report Forms (CRFs) collected during the study.
• Files interval (interim), annual reports, and/or final reports to the IRB/IEC, IND safety reports and other pertinent information throughout conduct of study.
• Attends the investigator’s meeting, pre-study site visit, study initiation visit, and all other study-related visits by Monitors or Sponsor representatives.
• Attends in-house protocol meeting to review study-related procedures, staffing and visit flow.
• Arranges for procedures performed by external vendors that are necessary to the conduct of the study.

 

 

 

 

What you will bring to the role

• Strong communication skills with excellent customer service
• Tenacity, with the ability to multi-task and adjust to a fast paced, virtual environment and constantly changing schedules
• Detail-oriented mindset
• A focus on creating effective relationships with a positive team player attitude
• Proficiency in MS Outlook, Excel, and Word

Your background

• Bachelor’s Degree (preferably in the field of Life Sciences or Health) with PRN Clinical Research experience.
• Preferred: 2 to 5 years of Clinical Research experience

Why Worldwide

At Worldwide, we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every clinical trial like a patient’s life depends on it – because it does. Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers.

Interested in hearing more about Worldwide or our roles? Check out our careers page at www.worldwide.com/careers!

City:

State:

Employment Type: PRN

Community / Marketing Title: PRN Clinical Research Coordinator

Company Profile:

We’re a global, mid-size CRO that pushes boundaries, innovates and invents — because the path to a cure for the world’s most persist diseases is not paved by those who play it safe, but by those who take pioneering, creative approaches, and implement them with quality and excellence. We are experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs, in the best possible way.

Location_formattedLocationLong: San Antonio, Texas US

CountryEEOText_Description: Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law. Worldwide is committed to working with and providing reasonable accommodations to applicants with disabilities. We are proud to be an equal opportunity workplace where people thrive by being themselves and are inspired to do their best work every day.