Research Associate 1

Requisition Number: 4430

Position Title: Research Associate 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.

 

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.

 What you will do:

The Research Associate 1, under the guidance of the Screening Manager 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.  The Research Associate 1 works under the general supervision and guidance of the Screening Manager. 

 

The Research Associate's responsibilities include, but are not limited to, the following: 

•  Conducts screening visits for the recruitment of a clinical trial under the supervision of the Screening Manager, reviews study protocol and informed consent form for studies they will be assigned to, attends in-house meetings and study initiation visits for their studies, prepares study specific screening documents and study folders.  During the screening phase, helps assure source documents for the trial are accurate and thorough, including maintenance of subject folders.
• Meets with Recruitment Services Supervisor and/or Recruitment Specialists to instruct on protocol specific phone screening questionnaire and scheduling of potential volunteers.  Responsible for reviewing subject screening forms prior to subject’s appointment to verify screening eligibility, Serves as a primary contact for subjects from screening through period 1 check-in for in-house studies, to handle subject eligibility, study specific questions, concerns or events, Contacts subjects prior to check-in to confirm subject’s ongoing participation.
• Responsible for reviewing the informed consent form, medical history, inclusion/exclusion and other study documents as required with subjects in order to assess eligibility, Covers subject visits (i.e. outpatient visits, check-ins, and check-outs) as assigned, Prepares for study check-in by completing study specific documents, supplies, and services needed for successful running of the study.
• Meets with Recruitment Services Supervisor and/or Recruitment Specialists to instruct on protocol specific phone screening questionnaire and scheduling of potential volunteers.  Responsible for reviewing subject screening forms prior to subject’s appointment to verify screening eligibility.

 

What you will bring to the role

• Excellent written and oral communication skills. Ability to understand complex written and oral instructions.  Basic computer knowledge and applications required for generation of business correspondence and preparation of regulatory and other study documents.  Strong interpersonal skills.
• Excellent attention to detail.  Exceptional organizational skills.  Ability to set and meet deadlines with high quality work.     
• Some knowledge of the clinical research process, including Good Clinical Practices.
• Possible equipment includes, but is not limited to:  computers, rolling carts, fax machine, photocopier, telephone, lab apparatus, mop/broom, needles, spirometry equipment, centrifuges, freezers, allergy testing equipment, scales, calculators, vital signs equipment, ECG machines, dishwasher, microwave, etc. 

 Your experience:

Required:            Bachelor’s Degree (preferably in the field of Life Sciences or Health).
 
Preferred:           Experience or class work in the health field.

City:

State:

Employment Type: Regular

Community / Marketing Title: Research Associate 1

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.