Top 3 Clinical trial manager Jobs in Tulsa, Ok

Project Manager
Oklahoma State University —Tulsa, OK
- Weekends as needed
- Mid-level
- 3 years
- Psychology
CV Quality Research & Risk Manager
Hillcrest Medical Center —Tulsa, OK
- Full-time
- Nursing
- RN License
- Hospital
- Health insurance
- Tuition reimbursement
5d

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Project Manager

Oklahoma State University -
Tulsa, OK

Apply Now

Job Details

Full-time

Qualifications

Data integrity assurance
Data validation techniques
Data quality management
Quality control management
Clinical data entry
Quality issues
Appointment scheduling
Technical Proficiency
Quality data entry

Full Job Description

Project Manager GS9070

493855

Tulsa

CENTER FOR HEALTH SCIENCES (CHS)

Staff Full-time

Bachelor's degree

Campus

OSU-Center for Health Sciences

Contact Name & Email

Jamie Childers [email protected]

Work Schedule

Monday through Friday, 8:00am-5:00pm with occasional evenings and weekends.

Appointment Length

Regular Continuous/Until Further Notice

Hiring Range

Commensurate with education and experience

Priority Application Date

While applications will be accepted until a successful candidate has been hired, interested parties are encouraged to submit their materials by to ensure full consideration.

Special Instructions to Applicants

For full consideration, please include a resume, cover letter and contact information for three professional references.

About this Position

The Project Manager is responsible for ensuring the smooth day-to-day functioning of all research activities in the lab, including up to four different research protocols at any given time under a research portfolio. This role has primary responsibility for operational integrity, protocol fidelity, and participant safety across multiple trials and longitudinal studies, which include pregnancy, childbirth, newborns, and substance use disorders. The Project Manager will assist the Project Director in overseeing the execution of each study component across protocols including participant management, data collection, biospecimen processing and storage, quality control, training, and operations.

Required Qualifications:

Master's degree- Psychology, Cognitive Science, Public Health, Education or related field.
(degree must be conferred on or before agreed upon start date)
3-5 years of previous research experience focusing on vulnerable populations such as pregnant individuals and/or individuals with substance use disorder.
Experience with data entry, data coding, and data quality control is required.

Skills, Proficiencies, and/or Knowledge:

Ability to manage multiple tasks and exceptional time-management skills is necessary.
Willingness to contribute to the research agenda on one night a week and one weekend a month.
Ability to resolve issues in a timely manner and ensure smooth data collection appointments.
Ability to navigate various data collection platforms and project management programs including REDCap, Clincard, and others as needed for the position.

Preferred Qualifications:

Prior experience supporting neuroimaging research, including MRI-based studies involving pregnant individuals, infants, children or clinical populations.
Experience supporting randomized controlled trials, clinical interventions, or treatment studies is strongly preferred.
Demonstrated experience working with IRBs on amendments, continuing review, and reportable events.
Direct experience with infant or perinatal populations is highly desirable.

Skills, Proficiencies, and/or Knowledge:

Familiarity with neuroimaging workflows, including participant preparation, safety screening, and scanning scheduling.
Comfort working in clinical settings (i.e., hospital settings, prenatal care environments) is preferred.

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