Clinical Research Coordinator

Principal Duties and Responsibilities:

* Patient screening and recruitment (in person and remotely by phone or Zoom)

* Recruit and gather data from study participants (in-person and remotely).

* Patient follow-up and facilitating intervention adherence.

* Maintain records and databases.

* Administer surveys to participants through electronic surveys (REDCap).

* Conduct literature and library searches.

* Ensurecompliancewithfederaland IRB regulations.

* Assist with IRB submissions, amendments, and continuingreviews.

* Assist with preparation of grant applications and manuscripts, including data analyses, literature searches and drafting of texts.

* Perform administrative support duties as required.

* Attend individual and team meetings.

* Maintain contact and follow-up with study team members, including national recruitment sites and advisory board members.

Qualifications:

Bachelors required

Can this role accept experience in lieu of a degree? No

Experience:
Some relevant research project work 0-1 year preferred.

Knowledge, Skills and Abilities:

The candidate should:

• Bilingual (Fluent in English and Spanish, preference for native speaking and/or fluent)
• Be well-organized, self-motivated, attentive to detail, and a self-starter.
• Be able to problem-solve, function in a fast-paced environment, and manage time/workload with minimal supervision.
• Have excellent interpersonal communication skills to effectively communicate with a multidisciplinary team and research participants.
• Have the ability to work independently, take initiative, and interact with clients and colleagues of multiple disciplines.

The CRC should be proficient in using administrative software (Excel, Word, Access, PowerPoint). Experience with webpage development, patient interaction, and IRB will provide the candidate with an advantage.

Availability to work in-person 4 out of 5 days a week are required. The working hours are typically 8:30-5pm, however, some tasks may fall outside of these hours due to patient scheduling.Some studies may occur in off-site healthcare settings and may include evening and / or weekend work.