Research Associate

Requisition Number: 5999

Position Title: Research Associate 1

External Description:

SUMMARY: Do you love science and making a difference? Are you analytical-minded, organized, and people-focused? Then apply today for our Research Associate 1 opportunity in San Antonio, TX.

 

About Worldwide Clinical Trials, Early Phase: Located in San Antonio, TX, Worldwide’s Clinical Pharmacology Unit is a top-notch clinical research organization focused on providing superior customer service to our participants and developing our internal team members to grow their careers. Founded by physicians we are focused on offering a unique experience to our employees and our participants.

 

About You: You are a forward-thinking, people-focused, organized, detail oriented individual with a passion for research and making a difference in the research industry. You should have familiarity with processing and reviewing clinical documentation, interacting with participants, and accommodating competing priorities in a dynamic clinical research environment. For more of the day-to-day responsibilities see below.
 
Responsibilities:
Tasks may include but are not limited to:

• Conducts screening visits for participant recruitment into clinical trials under the supervision of the Screening Supervisor.

• Always representing Worldwide Clinical Trials (WCT) in a professional manner (verbal, written, and in appearance) when interacting with sponsors, volunteers, outside vendors, and fellow employees.

• Reviews study protocol and informed consent form for studies they are assigned to.
• Attends meetings and study initiation visits for their studies as applicable. 
• Ensures electronic and paper source documents for the trial are accurate according to study specific protocol.
• Prepares and maintains study-specific screening documents and study folders. 
• Communicates with Recruitment Specialists throughout screening process to ensure appropriate scheduling of screening sessions and participant eligibility.
• Responsible for entering and updating participants in vendor study eligibility portal.
• Responsible for reviewing the informed consent form, medical history, inclusion/exclusion, and other study documents as required with participants to determine eligibility.

• Serves as primary contact for participants from screening through check-in for studies. Adresses all questions from participants related to study eligibility, study participation, and/or concerns.

Responsible for contacting participants for lab work, re-screening, and check-in to confirm the participant’s ongoing participation and eligibility.

Perform other duties as assigned.  The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

Additional Skills & Responsibilities

• Excellent written and oral communication skills. 
• Ability to understand complex written and oral instructions.
• Excellent attention to detail resulting in high-quality work. 
• Exceptional organizational skills. 
• Ability to set and meet deadlines.     

Educational Requirements:
Preferred: 

• Bachelor’s Degree (preferably in the field of Life Sciences or Health).
• Six months or more experience in health care.
  
  

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: Research Associate

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.