Clinical Research RN: Lead Trials Elevate Patient Care

Mercy

Ozark (MO)

In loco

USD 65.000 - 90.000

Tempo pieno

4 giorni fa
Candidati tra i primi
Generatore di candidature

Aumenta le possibilità di ricevere una risposta da questo datore di lavoro — un curriculum e una lettera di presentazione personalizzati, che corrispondono esattamente a ciò che sta cercando.

Supera i filtri ATS

Vantaggi offerti da questo lavoro

Medical insurance
Dental and vision
Tuition assistance
Retirement plan match

Descrizione del lavoro

Mercy is seeking a Clinical Research Registered Nurse to coordinate trial activities, ensure participant safety, and maintain data integrity. The role supports investigators, sponsors, and patients to drive successful outcomes.

Responsibilities include recruitment support, education, consent, and adherence to GCP and regulatory standards, with opportunities for training and mentoring within a collaborative Mercy Research team.

Competenze

  • RN license in the state of practice.
  • BSN or diploma with nursing experience.
  • Experience with clinical trials or willingness to learn.

Mansioni

  • Coordinate clinical research activities and patient visits.
  • Screen, consent, educate, and monitor study participants.
  • Administer investigational products and procedures per protocol.
  • Ensure protocol compliance, GCP, and regulatory requirements.
  • Collect, document, and manage study data and source records.
  • Monitor participant safety and report adverse events as required.
  • Collaborate with investigators, sponsors, CROs, and staff.
  • Support recruitment and community outreach efforts.
  • Assist with training and mentoring research team members.
  • Attend study meetings and perform other duties as assigned.

Conoscenze

Strong communication
Organizational skills
Problem solving
Team collaboration
Documentation

Formazione

Nursing Diploma/ADN/BSN

Strumenti

Microsoft Office

Descrizione del lavoro

Mercy is seeking a Clinical Research Registered Nurse to coordinate trial activities, ensure participant safety, and maintain data integrity. The role supports investigators, sponsors, and patients to drive successful outcomes.

Responsibilities include recruitment support, education, consent, and adherence to GCP and regulatory standards, with opportunities for training and mentoring within a collaborative Mercy Research team.

Ottieni la revisione del curriculum gratis e riservata.

o trascina qui il file.

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