Address
Form of workRequisition Number: 7467
Position Title:Associate Clinical Study Manager
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 over 3,000 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 the Clinical Study Management Department does at Worldwide
The Clinical Study Management department provides above-and-beyond clinical, technical, and customer support for all Phase I through IV Clinical Trials that may be local, regional, or global in scope. We are the face of WCT for our clients and subjects and we pride ourselves on providing a unique clinical experience for your study.
What the Associate Clinical Study Manager does at Worldwide
The Associate, Clinical Study Manager will support the Clinical Study Manager (CSM) on one or more allocated Phase I through IV Clinical Trials that may be local, regional, or global in scope.. Deputizes for the CSM with directing the technical, financial, and operational aspects to ensure the successful completion of the clinical trials. Works with functional area lead to identify and evaluate essential project prerequisites. The ACSM cooperates with the CSM to ensure all project deliverables meet the client's time/quality/cost expectations.
What you will do
Tasks may include but are not limited to:
What you bring to the role
Your 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: Regular
Community / Marketing Title:Associate Clinical Study Manager - San Antonio, TX - 100% Onsite
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.
Position Title:Associate Clinical Study Manager
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 over 3,000 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 the Clinical Study Management Department does at Worldwide
The Clinical Study Management department provides above-and-beyond clinical, technical, and customer support for all Phase I through IV Clinical Trials that may be local, regional, or global in scope. We are the face of WCT for our clients and subjects and we pride ourselves on providing a unique clinical experience for your study.
What the Associate Clinical Study Manager does at Worldwide
The Associate, Clinical Study Manager will support the Clinical Study Manager (CSM) on one or more allocated Phase I through IV Clinical Trials that may be local, regional, or global in scope.. Deputizes for the CSM with directing the technical, financial, and operational aspects to ensure the successful completion of the clinical trials. Works with functional area lead to identify and evaluate essential project prerequisites. The ACSM cooperates with the CSM to ensure all project deliverables meet the client's time/quality/cost expectations.
What you will do
Tasks may include but are not limited to:
- Ensure appropriate communication on project-related matters with CSM and CSM management
- manage and store signed approval forms for Lab, PK processing, Clinspark Go live, and Clinspark training and access request forms from clients
- Act as one of the key client contacts for assigned projects, schedule monitor visits and escort client contacts when they are on site as needed
- Coordinate and collate signature forms for SIV attendance, logistics meetings, and any other protocol training-related meetings, and file in the appropriate study folder
What you bring to the role
- Excellent communication, planning, and organizational skills
- Sense of urgency and ability to be adaptable in a fast-paced and rapidly changing environment
- Self-motivated and excellent problem-solving skills
- Ability to work independently
Your experience
- Bachelor's Degree (Life Sciences or Health preferred) with 3 years of clinical research experience or
- Associate degree with four years of clinical research experience and accredited Clinical Research credentials
- Or 6 years of clinical research experience instead of a degree
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: Regular
Community / Marketing Title:Associate Clinical Study Manager - San Antonio, TX - 100% Onsite
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.
