Clinical Research Coordinator, Pharmaceutical Research and Manufacturers of America (PhRMA) - Equitable Breakthroughs in Medicine Development (EQBMED) Clinical Trial Initiative

Updated: June 19

Houston

3100 Cleburne St

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84.4

0mi

Job Abstract

The Clinical Research Coordinator manages clinical research projects for Principal Investigators by gathering patient data via methods specified in the study protocol. Provides complex administrative duties in support of the study to ensure compliance with regulations. DISTINGUISHING CHARACTERISTICS:The Clinical Research Coordinator is a highly collaborative, self-motivated, creative person that is adaptable to new processes with capacity to function independently. This is a Grant Funded positio... more details

Clinical Research Coordinator, Pharmaceutical Research and Manufacturers of America (PhRMA) - Equitable Breakthroughs in Medicine Development (EQBMED) Clinical Trial Initiative

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Posting Details

Title Information

Security Sensitive Position?	Yes
Hours of Work	8:00 AM - 5:00 PM M-F

Position Details

Position Information

Posting Number	TSU203144
Official TSU Title	Clinical Research Coordinator, Pharmaceutical Research and Manufacturers of America (PhRMA) - Equitable Breakthroughs in Medicine Development (EQBMED) Clinical Trial Initiative
Grant Title	Clinical Research Coordinator, Pharmaceutical Research and Manufacturers of America (PhRMA) - Equitable Breakthroughs in Medicine Development (EQBMED) Clinical Trial Initiative
Job Description Summary / TWC Summary	JOB SUMMARY: The Clinical Research Coordinator manages clinical research projects for Principal Investigators by gathering patient data via methods specified in the study protocol. Provides complex administrative duties in support of the study to ensure compliance with regulations. DISTINGUISHING CHARACTERISTICS: The Clinical Research Coordinator is a highly collaborative, self-motivated, creative person that is adaptable to new processes with capacity to function independently. This is a Grant Funded position.
Essential Duties Summary	Applies knowledge in contributing to Good Clinical Practice (GCP) activities and/or other regulatory activities. Under the direction of the PI, supervises and assists with the preparation and submission of all IRB and Regulatory Documents to obtain final approval and may draft various communications with Sponsor. Attends and participates in the Investigator meeting. Reviews goals and requirements of any new protocols and coordinates study initiation. Identifies and recruits clinical research subjects for participation of studies, collects data, and monitors enrollment goals. Assesses staffing needs based upon current research activity and implements changes in staffing as needed. Participates in protocol initiation visits. Plans and designs source documentation for protocol. Develops assessment tool per protocol to use in clinical research and teaches research team and hospital personnel how to use the assessment tool as allowed per medical practice. Develops procedures for laboratory collection and storage. Assists in processing and shipping lab specimens; retrieves and/or sends identified research specimens certified if indicated as per regulations. Maintains accurate source documentation and appropriate forms as per protocol including participant records, drug documentation, reconciling study drug accountability; monitors documentation for quality and accuracy. Conducts reviews of on-going studies and oversees quality assurance on ongoing protocols; productive working relationship with the study monitor. Precepts new clinical research staff and educates research staff regarding scientific aspects of studies. Provides performance management for staff under direction of PI. Assesses communication process within Department and/or services required by the protocol. Elicits relevant data from sources outside of the hospital. Assists PI in budget development; may monitor ledgers. Assists in processing and shipping lab specimens efficiently and cost effectively; maintains supply inventory and equipment; ensures return of test article /clinical supplies; maintains regulatory standards. Identifies and recruits clinical research subjects; monitors enrollment goals and modifies recruitment strategies, as necessary; mentors all clinical research personnel regarding enrollment/recruitment. Monitors participants labs and notifies the PI of laboratory findings. Serves as a role model and resource for the clinical research staff. Obtains Informed Consent from study participant and documents appropriately. Adheres to internal controls established for department. Performs related duties as required.
% FTE	1.0
Hiring Range	$63,840.00 - $79,801.00
Education	Bachelor’s degree.
Required Licensing/Certification	N/A
Knowledge, Skills, and Abilities	Skill in: Demonstrated skills in computer software applications (e.g., Microsoft outlook, Teams, office 365) Detail oriented, Problem-solving, decision-making, multitasking and time management Excellent communication, both verbal and written, with strong public speaking skills Ability to: Ability to learn and adapt to new processes and adhere to organizational objectives Able to work in a team and produce quality output under tight deadlines Ability to work independently, collaboratively, and exercise sound judgment
Work Experience	Three (3) years’ experience as clinical research coordinator or equivalent experience. Bilingual e.g.: Spanish, Asian dialects, etc. preferred. Phlebotomy skills preferred. Demonstrated experience in effective conflict management and resolution
Working/Environmental Conditions	Routine office environment, Sitting or standing in one location much of the time Standard hospital, clinical, laboratory and/or office environments. Willingness to work flexible hours to meet the needs of the program Report directly to the Program Director/Principal investigator. Works closely with the team to prepare reports and deliverables to funding agency Some travel locally and to surrounding counties in the greater Houston area is expected (~45%) with mileage reimbursement
Desired start date
Position End Date (if temporary)

Posting Detail Information

UA EEO Statement	It is the policy of Texas Southern University to provide a work environment that is free from discrimination for all persons regardless of race, color, religion, sex, age, national origin, individuals with disability, sexual orientation, or protected veteran status in its programs, activities, admissions or employment policies. This policy of equal opportunity is strictly observed in all University employment-related activities such as advertising, recruiting, interviewing, testing, employment training, compensation, promotion, termination, and employment benefits. This policy expressly prohibits harassment and discrimination in employment based on race, color, religion, gender, gender identity, genetic history, national origin, individuals with disability, age, citizenship status, or protected veteran status. This policy shall be adhered to in accordance with the provisions of all applicable federal, state and local laws, including, but not limited to, Title VII of the Civil Rights Act. Manual of Administrative Policies and Procedures
Close Date
Open Until Filled (overrides close field)	Yes
Special Instructions to Applicants	Open to all applicants.

Posting Supplemental Questions

Required fields are indicated with an asterisk (*).

* Do you have a Bachelor's Degree?
- Yes
- No
* Do you have three (3) years’ experience as clinical research coordinator or equivalent experience?
- Yes
- No
* Are you fluent in bilingual e.g.: Spanish, Asian dialects, etc.?
- Yes
- No
* Are you skilled in Phlebotomy?
- Yes
- No

Applicant Documents

Required Documents

Resume
Cover Letter/Letter of Application
Official Transcripts

Optional Documents

Other Document
Reference Letter 1
Reference Letter 2
Reference Letter 3

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Search Terms: Clinical Research, Clinical, Research Coordinator, Research, Development

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Clinical Research Jobs: $15-$57/Hr. Multiple Positions Hiring Immediately

Houston

Hiring Immediately! Multiple Positions Available. $15-$57/Hr.