Clinical Research Monitor - CONNECT

Davita Inc.; Columbus (OH); On-site; USD 60,000 - 90,000; Full time

Job summary

A leading healthcare organization seeks a Clinical Research Monitor based in Columbus, OH. The role involves ensuring research quality through audits and evaluations of clinical protocols. Ideal candidates will possess a relevant bachelor's degree and significant experience in clinical research, ensuring compliance with industry standards.

Qualifications

• Bachelor's Degree in a health science or related field required.
• Three years of clinical research experience required.
• Two years of quality assurance experience preferred.

Responsibilities

• Reviews and evaluates research protocols, data, and reports.
• Develops and implements quality assurance procedures.
• Conducts audits of research studies for compliance.

Education

Bachelor's Degree in a health science or related field

Job description

Overview:

CONNECT is an international collaborative network of pediatric cancer centers whose objective is improving outcomes for children with high-risk brain tumors. The Operations center for this network is located at Nationwide Children's Hospital in Columbus, OH.

The Clinical Research Monitor will be responsible for ensuring research quality by reviewing documentation, conducting monitoring visits, and providing feedback to improve processes. The ideal candidate will have a background in clinical research and regulatory compliance.

Job Description Summary:

Ensures research quality by reviewing documentation, conducting audits, and providing feedback to improve processes.

Job Description:

Essential Functions:

• Reviews and evaluates research protocols, data, and reports to ensure compliance with regulatory requirements and industry standards.
• Develops and implements quality assurance procedures to identify and address potential issues in research studies.
• Conducts audits of research studies to ensure accuracy, completeness, and consistency of data.
• Prepares audit reports and communicates findings to management and research staff.
• Collaborates with research teams to develop corrective action plans to address identified issues.
• Maintains up-to-date knowledge of regulatory requirements and industry standards related to research quality assurance.

Education Requirement:

Bachelor's Degree in a health science or related field, or equivalent experience, required.

Licensure Requirement:

(not specified)

Certifications:

(not specified)

Skills:

(not specified)

Experience:

• Three years of clinical research experience, required.
• Two years of quality assurance experience withhuman subjectsresearch, preferred.

Physical Requirements:

OCCASIONALLY: Bend/twist, Climb stairs/ladder, Squat/kneel

FREQUENTLY: Lifting / Carrying: 0-10 lbs, Lifting / Carrying: 11-20 lbs, Pushing / Pulling: 0-25 lbs, Pushing / Pulling: 26-40 lbs, Standing, Walking

CONTINUOUSLY: Audible speech, Color vision, Computer skills, Decision Making, Depth perception, Flexing/extending of neck, Hand use: grasping, gripping, turning, Hearing acuity, Interpreting Data, Peripheral vision, Problem solving, Reaching above shoulder, Repetitive hand/arm use, Seeing - Far/near, Sitting

Additional Physical Requirements performed but not listed above:

(not specified)

"The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this classification. It is not to be construed as an exhaustive list of duties performed by the individuals so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under their supervision. EOE M/F/Disability/Vet"