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Elligo Jobs (NOW HIRING)

Elligo Health Research

Patient Engagement Associate

$17.50 - $22/hr

Elligo Health Research is a dynamic organization in a rapidly changing industry. Accordingly, the responsibilities associated with this job may change from time to time in accordance with business ...

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What jobs make $3,000 a month without a degree?

Jobs such as sales representatives, delivery drivers, and administrative assistants can earn around $3,000 monthly without requiring a degree. These roles often rely on experience, skills, or certifications rather than formal education and may involve flexible schedules or commission-based pay structures.

What are the key skills and qualifications needed to thrive as a Clinical Research Coordinator at Elligo, and why are they important?

To thrive as a Clinical Research Coordinator at Elligo, you need a solid background in clinical research, regulatory compliance, and data management, often supported by a degree in life sciences or nursing. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC), and GCP certification is typically required. Strong organizational skills, attention to detail, and effective communication help you manage studies and build relationships with sponsors and participants. These competencies ensure studies are conducted efficiently, ethically, and in compliance with regulatory standards.

What is the difference between Elligo vs Clinical Research Coordinator?

AspectElligoClinical Research Coordinator
CredentialsTypically requires a healthcare background, such as RN or medical assistant certificationRequires a bachelor's degree in health or related field; certifications like CCRP are common
Work EnvironmentWorks with healthcare providers and patients, often remotely or in clinicsWorks directly in clinical settings, managing research activities on-site
Employer & IndustryContracted by pharmaceutical companies, CROs, or healthcare organizationsEmployed by research sites, hospitals, or clinics conducting clinical trials

Elligo professionals focus on facilitating clinical trials through healthcare provider networks, often working remotely or in clinics. Clinical Research Coordinators manage trial activities directly at research sites. Both roles require healthcare knowledge but differ in work setting and employer type.

What holistic job makes the most money?

In the holistic health field, licensed practitioners such as naturopathic doctors, acupuncturists, and chiropractors tend to earn the highest salaries. These roles often require advanced certifications, clinical experience, and sometimes a private practice setup, which can lead to higher income levels compared to other holistic health careers.

What are some typical challenges faced by professionals working at Elligo in clinical research roles?

Professionals at Elligo in clinical research often encounter challenges such as coordinating between multiple stakeholders, managing tight study timelines, and ensuring strict regulatory compliance. Navigating the complexities of patient recruitment and maintaining high-quality data integrity are also common hurdles. However, Elligo's collaborative team environment and access to advanced resources help address these challenges, fostering professional growth and learning opportunities.

What is an Elligo Clinical Research Professional?

An Elligo Clinical Research Professional is someone who works for Elligo Health Research, a company that connects healthcare practices and patients with clinical research opportunities. These professionals may serve in various roles such as clinical research coordinators, project managers, or support staff, helping to facilitate clinical trials and ensure regulatory compliance. Their responsibilities often include recruiting patients, managing study protocols, and collaborating with sponsors and investigators to advance medical research. By bridging the gap between healthcare and research, Elligo professionals help accelerate the development of new medical treatments.
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Infographic showing various Elligo job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.
Clinical Research Coordinator II

Clinical Research Coordinator II

Elligo Health Research

Katy, TX • On-site

$21 - $27.75/hr

Full-time

Posted 12 days ago

Job 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 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:
ESSENTIAL DUTIES
  • Develop strong working relationships and maintain effective communication with study team members.
  • Develop strong working relationships and become the point of contact for the clinic as well as the sponsor for clinic related activities.
  • Manage multiple concurrent trials
  • Assist with mentoring and training study team members
  • Complete all protocol-related training
  • Perform patient/research participant scheduling
  • Collect patient/research participant history
  • Collects and maintains source documentation
  • Performs data entry and query resolution
  • Collect and review required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, non-clinical supply materials, imaging, and laboratory handling manuals, etc.).
  • Adhere to an IRB-approved protocol
  • Conduct the informed consent process of research subjects.
  • Support the safety of research subjects, report adverse events
  • Coordinate protocol-related research procedures, study visits, and follow-up and anticipate and mitigate potential non-compliance
  • Assist with the screening, recruiting, and enrollment of research subjects.
  • Facilitate pre-study, site qualification, study initiation, monitoring visits, and study close-out activities
  • Collect, process, and ship laboratory specimens
  • Follow ethical and professional codes of conduct and escalate noncompliance as needed
  • Communicate with Stakeholders: CRAs, Project Managers, Patient Services, Account Managers, healthcare practices
  • Adhere to the study plan by ensuring that all approvals are in place, vendors are qualified
  • Comply with Elligo, Clinic, and Sponsor policies, standard operating procedures (SOPs), GCP guidelines, and documents data according to ALCOA.
  • Comply with Elligo, Clinic, and Sponsor policies, standard operating procedures (SOPs), and guidelines.

WORKING CONDITIONS
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
KNOWLEDGE SKILLS AND ABILITIES REQUIRED
  • Minimum 3 years of experience coordinating clinical trials, including the activities listed above
  • BS/BA in Life Science or related discipline or equivalent work experience
  • Previous nursing experience in a clinical setting a plus
  • CCRC certification a plus
  • Demonstrated ability in positive relationship building, with strong verbal and written skills required.
  • Knowledge of clinical trial terminology and practices required
  • Demonstrated ability to coordinate complex protocols with overlapping timelines
  • Prior GCP training and ability to explain importance of GCP guidelines
  • Management of regulatory documents throughout trial lifecycle
  • Ability to train others on key protocol elements and study task execution
  • Able to clearly explain and enforce clinical research participant safety requirements including safety reports, ICF elements and role of the IRB
  • Strong interpersonal skills with attention to detail a must
  • Follow ethical and professional codes of conduct
  • Take action to minimize participant risk
  • Adhere to the study plan by ensuring that all approvals are in place, vendors are qualified
  • Comply with Elligo, Clinic, and Sponsor policies, standard operating procedures
  • (SOPs), GCP guidelines and documents data according to ALCOA
  • Demonstrated proficiency with word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, and SharePoint) and with clinical trial master filing systems.
  • Ability to travel for Clinic activities, and attend investigator meetings or vendor visits/audits, as required.
  • Strong organization/prioritization skills for the management of multiple concurrent projects

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