Nurse Clinical Research I Jobs in Arkansas

Conduct all types of visits including, qualification, initiaiton, monitoring and close out

Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff

Ensure good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements

Minimum 1.5 years monitoring experience

Strong verbal and written communication skills

8-12 days on site per month

Bachelor’s degree plus 3-5 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or

Associate’s degree plus 5 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or

High School diploma/GED plus 7 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection

Bachelor’s degree plus 5 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management and data collection

Knowledge and skill with word processing, spreadsheet, database, and e-mail computer software (e.g., Microsoft Word, Excel, Access, Outlook)

UAMS offers amazing benefits and perks

Knowledge of clinical research study processes, protocol management, and regulatory guidelines.

Proficiency in medical terminology and computer skills.

Strong attention to detail and excellent written and oral communication skills.

Ability to manage multiple deadlines and prioritize tasks effectively.

Minimum three years of experience in conducting clinical research studies or verifying clinical data.

Knowledge across multiple therapeutic areas, including blood and marrow transplant.

Assists with coordination and management of clinical trials including communication with Sponsors.

Under direct supervision of the Principle Investigator(s), obtains informed consent and educates participants regarding study requirements.

0-2 years of experience in a hospital or academic (research) environment preferred.

Excellent written and oral communication skills

Collects and records study data; inputs all information into database.

Secures, delivers and ships clinical specimens as required by the protocol.

Excellent organizational, time management, and problem-solving skills.

Support and comply with the company’s Quality Management System policies and procedures.

Basic proficiency of ICH GCP and monitoring practices with a track record for ensuring quality data and performing outstanding site management.

Supports the Clinical Study Manager to develop study-specific training materials.

Conducts thorough site qualifications visits. Ensures all required information concerning site/staff qualifications is clearly documented and communicated to project teams.

Works with clinical study manager to manage vendors (ie. Central Laboratory, CRF printers, CROs, etc).

Obtain informed consent and educate participants regarding study requirements.

1-2 years clinical research experience

Pristine attention to detail and ability to manage time appropriately, able to multitask in a fast-paced environment

Collect and record study data and input all information into a database.

Assist in IRB/GCO applications as needed.

Collect, process, deliver and ship clinical specimens as required by the protocol.

Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.

1-2 years of research experience

Collects and records study data. Inputs all information into database.

Assists in preparing grant applications, IRB/GCO for submission and filings.

Secures, delivers and ships clinical specimens as required by the protocol.

Bachelors or Masters degree in Science or closely related field.

Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.

1-2 years of research experience

Collects and records study data. Inputs all information into database.

Assists in preparing grant applications, IRB/GCO for submission and filings.

Secures, delivers and ships clinical specimens as required by the protocol.

Bachelors or Masters degree in Science or closely related field.

Strong communication and organization skills

Obtain informed consent and educate participants regarding study requirements.

1-2 years clinical research experience

Pristine attention to detail and ability to manage time appropriately, able to multitask in a fast-paced environment

Background in clinical research or closely related field

Passion for patient care and clinical research

Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.

1-2 years of research experience

Collects and records study data. Inputs all information into database.

Assists in preparing grant applications, IRB/GCO for submission and filings.

Secures, delivers and ships clinical specimens as required by the protocol.

Bachelors or Masters degree in Science or closely related field.

Obtain informed consent and educate participants regarding study requirements.

Strong communication and organization skills

1-2 years clinical research experience

Pristine attention to detail and ability to manage time appropriately, able to multitask in a fast-paced environment

Collect and record study data and input all information into a database.

Assist in IRB/GCO applications as needed.

Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.

1-2 years of research experience

Collects and records study data. Inputs all information into database.

Assists in preparing grant applications, IRB/GCO for submission and filings.

Secures, delivers and ships clinical specimens as required by the protocol.

Bachelors or Masters degree in Science or closely related field.

Assists with coordination and management of clinical trials including communication with Sponsors.

Under direct supervision of the Principle Investigator(s), obtains informed consent and educates participants regarding study requirements.

1-2 years of research experience

Experience in a hospital or academic (research) environment preferred

Excellent written and oral communication skills

Collects and records study data; inputs all information into database.

Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.

1-2 years of research experience

Collects and records study data. Inputs all information into database.

Assists in preparing grant applications, IRB/GCO for submission and filings.

Secures, delivers and ships clinical specimens as required by the protocol.

Bachelors or Masters degree in Science or closely related field.

Work with ARO data management team to ensure that all external sites have appropriate access to REDCap and Florence eBinders

1-2 years of relevant clinical research experience, preferably at least 1 year clinical trial monitoring or CRC experience

Background in clinical trial experience required

Experience working with CTMS and eTMF systems

Meet expected timelines for completion of monitoring activities and submission of written monitoring reports

Provide recommendations and guidance to study specific teams and assist in audit readiness and preparation