Job description

An individual who, under the direction and ongoing supervision of the Principal Investigator, aids in the daily function of clinical research programs being performed by Alliance Clinical Network.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Responsibilities may include, but are not limited to the following:

1. Able and willingness to work with COVID patients.

2. Communicates effectively and courteously with study patients and sponsors.

3. Obtain Informed Consent.

4. Collects patient medical history and conditions.

5. Study drug dispensation and accountability.

6. Collect and evaluate concomitant medication.

7. Collect and evaluate medical records for compliance.

8. Conduct A/E and SAE for assessments.

9. Perform EKG, vital signs and protocol specific procedures.

10. Collect and process blood, urine and other specimens.

11. Evaluate clinical lab reports.

12. Maintains office site regulatory files.

13. Verify accuracy of data collected, data entry, query resolutions.

14. Document temperatures for IP stored on-site.

15. Recruit study patients.

16. Manage all required study startup documentation, training, and timelines on assigned study protocols.

17. Minimum of two years in clinical research coordinator experience (medical research involving people). Experience leading studies.

17. Other tasks and responsibilities as requested by Alliance Clinical Network to facilitate business needs.

QUALIFICATIONS AND SKILLS (May include, but are not limited to):

1. Strong written and verbal skills.

2. Comprehensive knowledge of FDA, GCP and HIPAA as applied to clinical research.

3. Knowledge of current studies being conducted.

4. Comprehensive knowledge of company's SOPs, Policies and Confidentiality agreements.

5. Knowledge of safety hazards and procedures that establish a safe work environment.

6. Skilled in computer and data collection software.

7. Phlebotomy, EKG, and other technical skills as required per protocol.

CERTIFICATES, LICENSES, REGISTRATION (May include, but are not limited to):

1. Minimum of two years in clinical research coordinator experience (medical research involving people). Experience leading studies.

2. CPR and first aid certification.

3. IATA and/or Safe-T-Pak certification for shipment lab specimens and/or dry ice.

4. GCP and protection of Human Subject Participants.

PREFERRED SKILLS

1. Detailed oriented

2. Phlebotomy

3. Prior knowledge of medical terminology

4. Ability to operate with limited direction

5. Good customer service skills

6. Problem solver

7. Quick learner

8. Multi-task

9. Spanish is a plus

Job Type: Full-time

Pay: $24.00 - $28.00 per hour

Benefits:

• Health insurance
• Paid time off

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday
• Weekend availability

Supplemental pay types:

• Bonus pay

Ability to commute/relocate:

• Dallas, TX 75230: Reliably commute or planning to relocate before starting work (Required)

Application Question(s):

• Are you willing and able to work with Covid patients?

Education:

• Associate (Preferred)

Experience:

• Phlebotomy: 5 years (Preferred)
• Clinical Research Coordinator: 5 years (Preferred)

Language:

• Spanish (Preferred)

Work Location: In person

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