Clin Research Data Coord II

All the benefits and perks you need for you and your family:

• Benefits from Day One
• Paid Days Off from Day One
• Student Loan Repayment Program
• Career Development
• Whole Person Wellbeing Resources

Our promise to you:

Joining AdventHealth is about being part of something bigger. It’s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind, and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that together we are even better.

Schedule: Full-time

Shift : Days

Location: 2525 S DOWNING ST, Denver, 80210

The role you’ll contribute:

The Clinical Research Data Coordinator II is responsible for the completeness, timely delivery, and quality of clinical research data via data entry. The Clinical Research Data Coordinator II is responsible for all aspects involved in ensuring high data quality, inclusive of the collection, abstraction, review, documentation and monitoring/auditing of data related to clinical research projects. In this role, the Clinical Research Data Coordinator II collaborates with study Investigators, Clinical Research Coordinator(s) (CRC), study sponsors, and other research and clinical team members in the conduct of Phase I-IV industry-sponsored, grant funded (federal or other grants), and/or investigator-initiated clinical trials in accordance with trial protocols, Food and Drug Administration (FDA) regulations, and International Conference on Harmonization/Good Clinical Practices (ICH/GCP) Guidelines. Actively participates in outstanding customer service and accepts responsibility in maintaining relationships that are equally respectful to all.

The value you’ll bring to the team:

• Serving as preceptor for all new data coordinators, including the development of training processes and material.
• Obtains all the essential, protocol required information as outlined by the approved study protocol and within the contractual obligations set forth.
• Promotes Principal Investigator oversight by advising study investigators, Supervisor(s) and/or Operation Manager(s) of deviations in conduct and/or various issues relevant to the data integrity of the trial; abides by hospital and departmental policies and SOPs, as well as all applicable local, state, and federal regulations.
• Actively contributes toward tasks related to ensuring compliance before, during, and after site monitor visits and/or audits conducted by the institution, industry sponsors, the FDA and other authorities.

Qualifications

The expertise and experiences you’ll need to succeed:

• Bachelor’s degree in healthcare related field, data processing or related field and at least one (1) year of administrative/professional experience with data related responsibilities (e.g. research, statistics, registry) or clinical research experience, OR
• Associate degree in health science, or related field, and at least two (2) years of administrative/professional experience with data related responsibilities (e.g. research, statistics, registry) or clinical research experience, OR
• Graduate of an accredited allied health certificate program and three (3) years of administrative/professional experience with data related responsibilities (e.g. research, statistics, registry) or clinical research experience, OR
• Three (3) years of direct clinical research data entry experience OR four (4) years of equivalent administrative/professional experience working with data or medical information to include duties such as data collection, management and verification.

This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances. The salary range reflects the anticipated base pay range for this position. Individual compensation is determined based on skills, experience and other relevant factors within this pay range. The minimums and maximums for each position may vary based on geographical location.

Category: Research

Organization: AdventHealth Rocky Mountain

Schedule: Full-time

Shift: 1 - Day

Req ID: 25004586

We are an equal opportunity employer and do not tolerate discrimination based on race, color, creed, religion, national origin, sex, marital status, age or disability/handicap with respect to recruitment, selection, placement, promotion, wages, benefits and other terms and conditions of employment.