Clinical Research Coordinator

Northwest Clincal Trials; Boise (ID); On-site; USD 60,000 - 75,000; Full time

Benefits offered by this job

Health, dental, and vision insurance

Holiday pay

Paid vacation time

Retirement plan with company matching

Job summary

Northwest Clinical Trials in Boise, Idaho is seeking a motivated Clinical Research Coordinator to manage all aspects of clinical trials, from planning to execution, in collaboration with physicians, nurses, and study staff.

The role emphasizes data accuracy, participant communication, and adherence to GCP guidelines, with opportunities to contribute to medical advancements while working in a fast-paced, collaborative environment.

Qualifications

• Knowledge of Good Clinical Practice (GCP) guidelines and regulations.
• Excellent organizational and multitasking skills.
• Strong attention to detail and ability to maintain accurate records.
• Exceptional interpersonal and communication skills, both written and verbal.
• Proficiency in using electronic data capture systems and other research software.

Responsibilities

• Manage all aspects of clinical trials, including planning, recruitment, and administrative tasks.
• Conduct screening interviews with potential study participants to assess eligibility.
• Coordinate patient enrollment and ensure documentation is obtained.
• Collaborate with physicians, nurses, and other research staff to ensure proper execution of trials.
• Collect and record accurate data during trials, following established protocols and guidelines.
• Monitor and evaluate patient progress throughout the trials, providing timely updates to the research team.
• Maintain detailed records of trial operations, including patient files, consent forms, and regulatory documents.

Skills

GCP knowledge

Organizational skills

Attention to detail

Interpersonal communication

Data management

Multitasking

Independent and collaborative work

Tools

Electronic Data Capture (EDC) systems

Job description

Northwest Clinical Trials is seeking a motivated and detail-oriented Clinical Research Coordinator to join our team. As a leading research organization in the pharmaceutical research industry, we are dedicated to improving patient care through clinical trials. In this role, you will have the opportunity to work on groundbreaking research projects and contribute to medical advancements. If you have a strong passion for healthcare, attention to detail, and excellent organizational skills, we want to hear from you!

As a Clinical Research Coordinator, you will be responsible for managing all aspects of clinical trials, from planning to execution. You will work closely with physicians, nurses, patients, and other research staff to ensure the smooth operation of trials and the collection of accurate data. Your exceptional communication skills will be essential as you will act as the point of contact for study participants, providing them with detailed information about the trials and addressing any concerns they may have.

Responsibilities

• Manage all aspects of clinical trials, including planning, recruitment, and administrative tasks
• Conduct screening interviews with potential study participants to assess their eligibility for trials
• Coordinate patient enrollment and ensure all necessary documentation is obtained
• Collaborate with physicians, nurses, and other research staff to ensure proper execution of trials
• Collect and record accurate data during trials, following established protocols and guidelines
• Monitor and evaluate patient progress throughout the trials, providing timely updates to the research team
• Maintain detailed records of trial operations, including patient files, consent forms, and regulatory documents

Preferred Experience

• Previous experience in clinical research coordination is preferred

Skills

• Knowledge of Good Clinical Practice (GCP) guidelines and regulations
• Excellent organizational and multitasking skills
• Strong attention to detail and ability to maintain accurate records
• Exceptional interpersonal and communication skills, both written and verbal
• Proficiency in using electronic data capture systems and other research software
• Ability to work independently and collaboratively in a fast-paced environment

Benefits

• - Health, dental, and vision insurance
• - Holiday pay
• - Paid vacation time
• - Retirement plan with company matching after one year