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Clinical Research Coordinator II, (Austin, TX)

Job Title
Clinical Research Coordinator II, (Austin, TX)
Job ID
27694781
Location
Austin,  TX 78738
Other Location
Description
JOB SUMMARY

The Clinical Research Coordinator II assists 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, ability to prioritize, “can-do” attitude, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills.

RESPONSIBILITES
  • Develop strong working relationships and maintain effective communication with study team members.
  • Become the point of contact for the clinic as well as the sponsor for clinic related activities.
  • Manage multiple concurrent trials.
  • Completes 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.
  • Support the collection and review of 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.
  • Assist in 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.
  • 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.
  • Comply with Elligo, Clinic, and Sponsor policies, standard operating procedures (SOPs) and guidelines.

KNOWLEDGE SKILLS AND ABILITIES REQUIRED
  • Associates Degree or BS/BA in Life Science or related discipline
  • Strong interpersonal skills with attention to detail a must.
  • Demonstrated proficiency with word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, SharePoint) and with clinical trial master filing systems.

WORKING CONDITIONS

This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, and photocopiers.

Some flexibility in hours may be required depending on study needs, possible occasional weekends, and the employee must be available during the “core” work hours of 8:00 a.m. to 4:00 p.m. All full-time employees must work a minimum of 37.5 hours each week to maintain full-time status. Occasional evening and weekend work may be required as job duties demand.

Travel: Local travel, as required.

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.

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.

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“I am super passionate about what we are doing at Elligo and feel so fortunate to be a part of it! I haven’t been this excited about a job in years!”

Janet L.
Client Relations Specialist

“Having been involved in clinical research for over 10 years, I have found the Elligo model to be truly innovative. From top to bottom, the Elligo team is made up of professionals who use their experience and knowledge to positively affect the need to bring healthcare and clinical research together.”

James C.
Director, Clinical Operations

“Elligo is at the forefront of innovation in the clinical research industry. It’s rewarding to work among such highly motivated and distinguished leaders and visionaries. I start work each day feeling valued and end each day excited to be part of Elligo’s influence on changing the clinical research industry.”

Julie M.
Study Manager, Clinical Operations

“Working at Elligo has been a very unique experience. I love the fact that I’m surrounded by colleagues who help me learn something new every day. I value their experience and genuinely enjoy the work and projects we are involved with. I love coming to work every day!”

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Business Analyst, Business Development

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