Austin, Texas, United States · On-site
Description JOB SUMMARY (To perform this job satisfactorily, an individual must be able to perform each essential duty satisfactorily. Other duties may be assigned.) This individual will play a key role in the conduct of…
Skills: Clinical Trial Coordination, Patient Scheduling, Data Entry, Informed Consent Process, GCP Guidelines
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The Clinical Research Coordinator II manages clinical trial activities, ensuring adherence to protocols, regulations, and corporate goals. Key duties include patient recruitment, data entry, coordinating study visits, and maintaining strong relationships with sponsors and clinic staff.
Requires a minimum of 3 years of clinical trial coordination experience and a bachelor's degree in Life Science or a related field. Proficiency in GCP guidelines, regulatory documentation, and MS Office is essential, with CCRC certification and nursing experience preferred.
Description
(To perform this job satisfactorily, an individual must be able to perform each essential duty satisfactorily. Other duties may be assigned.)
This individual will play a key role in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, the ability to prioritize, a “can-do” attitude, the ability to adapt quickly to changing business conditions, and strong interpersonal and team-building skills.
The CRC II will have overall responsibilities for coordinating efforts with other study team members in order to achieve protocol objectives and corporate goals, including:
The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel. More in-depth information can be found in SOP's, working guidelines, policies, etc.
Traveling CRC II positions will require (50%) travel for this position. Non-traveling will require (15- 25%) travel.
Elligo is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Elligo are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Elligo will not tolerate discrimination or harassment based on any of these characteristics. In addition, Elligo will provide reasonable accommodations for qualified individuals with disabilities.
Requirements
Elligo Health Research is an integrated research organization founded to bridge the gap between cutting-edge clinical trials and the patients who need them—an idea that sparked when our founder's barber couldn't access a promising treatment. By embedding research into routine care, Elligo empowers physicians to offer trials to their own patients, expanding access, improving diversity, and reducing barriers through additional travel and retention support services. Sponsors and CROs benefit from a nationwide network of research-ready sites—traditional and decentralized— backed by EHR data integration and proven recruitment strategies. With flexible service models, Elligo supports each site’s unique needs, from infrastructure and staffing to full-service trial operations. Our mission is to accelerate clinical research and bring life-changing therapies to more people, faster.
Offices: 11612 Bee Cave Rd, Austin, Texas 78738, US
Elligo Health Research is an integrated research organization founded to bridge the gap between cutting-edge clinical trials and the patients who need them—an idea that sparked when our founder's barber couldn't access a promising treatment. By embedding research into routine care, Elligo empowers physicians to offer trials to their own patients, expanding access, improving diversity, and reducing barriers through additional travel and retention support services. Sponsors and CROs benefit from a nationwide network of research-ready sites—traditional and decentralized— backed by EHR data integration and proven recruitment strategies. With flexible service models, Elligo supports each site’s unique needs, from infrastructure and staffing to full-service trial operations. Our mission is to accelerate clinical research and bring life-changing therapies to more people, faster.
Offices: 11612 Bee Cave Rd, Austin, Texas 78738, US
