Top 92 Clinical research coordinator Jobs in San Antonio, Tx

Clinical Research Coordinator 1
Worldwide Clinical Trials —San Antonio, TX
- $24.04 - $47.60 an hour
- Weekends as needed
- 18 years or older
- Computer literacy
- Mid-level
11d
Clinical Research Coordinator I - MTBI2
Henry M. Jackson Foundation —San Antonio, TX
- $52,800 - $70,000 a year
- Full-time
- Entry level
- Health insurance
- Dental insurance
10d
Clinical Research Coordinator
Bering-Alaka`ina Holdings, LLC —San Antonio, TX
- Current TB test
- Mid-level
- Bachelor's degree
- Paid holidays
- Disability insurance
13h
Clinical Research Coordinator Assistant
Flourish Research —San Antonio, TX
- Full-time
- Vital signs
- Bachelor's degree
- Data entry
- Disability insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator
U.S. Renal Care, Inc. —San Antonio, TX
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Customer service
14d
CTO Clinical Research Coordinator-Associate (Mays Cancer Center)
University of Texas Health Science Center at San Antonio —San Antonio, TX
- 8 hour shift
- Anatomy knowledge
- HIPAA
- Mid-level
- AD&D insurance
- Paid holidays
4d
Clinical Research Coordinator
Pinnacle Clinical Research —San Antonio, TX
- Full-time
- Spanish
- Vital signs
- BLS Certification
- Paid holidays
- Disability insurance
Quick Apply
12d
Research Coordinator
University of Texas Health Science Center at San Antonio —San Antonio, TX
- 8 hour shift
- Microsoft Excel
- Customer service
- Mid-level
- AD&D insurance
- Paid holidays
12d
Clinical Research Coordinator
START Center for Cancer Research —San Antonio, TX
- Monday to Friday
- Mid-level
- High school diploma or GED
- 2 years
- Health savings account
- Paid holidays
Quick Apply
Clinical Research Coordinator
Tekton Research Inc —San Antonio, TX
- Full-time
- Nursing
- Mid-level
- High school diploma or GED
Quick Apply
Clinical Data Coordinator I (CS3622 - Hamilton Wolfe)
CommuniCare Health Centers (Texas) —San Antonio, TX
- Spanish
- Medical office experience
- HIPAA
Quick Apply
Clinical Research Coordinator
Urology San Antonio —San Antonio, TX
- Full-time
- Mid-level
- 3 years
- Travel
Quick Apply
CTO Clinical Research Coordinator-Associate (Mays Cancer Center)
UT Health Science Center at San Antonio —San Antonio, TX
- 8 hour shift
- Anatomy knowledge
- HIPAA
- Mid-level
- AD&D insurance
- Paid holidays
4d
Clinical Research Assistant
Medical Center Ophthalmology Associates —San Antonio, TX
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Health savings account
- AD&D insurance
13d
Research Coordinator
UT Health Science Center at San Antonio —San Antonio, TX
- 8 hour shift
- Microsoft Excel
- Customer service
- Mid-level
- AD&D insurance
- Paid holidays
11d
Clinical Coordinator Float
TSAOG Orthopedic & Spine —San Antonio, TX
- $17.00 - $29.47 an hour
- Overtime
- Mid-level
- High school diploma or GED
- Clinic
Quick Apply
Clinical Coordinator
Sports Medicine Associates of San Antonio —San Antonio, TX
- 8 hour shift
- LVN
- RN License
- BLS Certification
- Disability insurance
- Health insurance
Quick Apply
Clinical Nurse Coordinator Med Surg Oncology
Methodist Hospital Stone Oak —San Antonio, TX
- Full-time
- Mid-level
- Medical-Surgical
- 1 year
- Employee stock purchase plan
- Disability insurance
Quick Apply
Clinical Nurse Coordinator Med Surg ICU
Methodist Hospital —San Antonio, TX
- Full-time
- Mid-level
- Critical & Intensive Care
- Medical-Surgical
- Employee stock purchase plan
- Disability insurance
Quick Apply
Clinical Nurse Coordinator Lung Rescue ICU
Methodist Hospital —San Antonio, TX
- Full-time
- Mid-level
- Critical & Intensive Care
- 1 year
- Employee stock purchase plan
- Disability insurance
Quick Apply

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Clinical Research Coordinator 1

Worldwide Clinical Trials -
San Antonio, TX

Apply Now

Job Details

Full-time
$24.04 - $47.60 an hour
11 days ago

Qualifications

Computer operation
Desktop applications
Computer skills

Full Job Description

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!

SUMMARY: The Clinical Research Coordinator 1 (CRC 1), under the guidance of the Clinical Research Coordinator Supervisor or designee, and each clinical trial’s Principal Investigator, is responsible for assisting with assuring that the integrity and quality of the clinical research trial is maintained and that the trial is conducted in accordance with Good Clinical Practice guidelines and ICH guidelines as applicable.

RESPONSIBILITIES:
Tasks may include but are not limited to:

Always represents Worldwide Clinical Trials (WCT) in a professional manner (verbal written and in appearance) when interacting with subjects, outside vendors and fellow employees Verification.
Reviews study protocol.
Performs quality checks on source documents specific to the study, per SOP review must occur in a defined timeframe.
Attends in-house protocol meeting to review study-related procedures, staffing and visit flow and sponsor SIV.
Responsible for giving subject instructions at check-in and serves as the primary contact for subjects by being available to handle study-specific questions, concerns, or events.
Responsible giving subjects’ safety orientation upon checking into the Clinic.
Obtains and documents adverse event data on appropriate forms.
Payment to subjects.
Responsible for completing continuous training assignments.
Covers OPV, checkouts and check-ins, dosings.
Tracking infractions to in-house.
Responsible for scheduling clinical lab reports as ordered by physician.
Conducting study check-ins.
Back Up contact for subjects.
Responsibilities for t-shirt allocation.
Answering queries and laundry schedule.
Other duties as assigned.

Other: Possible mental demands include, but are not limited to: reading, math, intense concentration, verbal communication, written communication, attention to detail, multiple tasks, frequent interruptions, and fluctuation in work load.

Possible physical demands include but are not limited to: occasional lifting and carrying of objects weighing 5-50 lbs.; hearing; seeing; gross and fine motor use of upper extremities; kneeling; walking; standing; leaning over for extended periods; squatting; eye strain/fatigue; climbing; pushing; pulling; reaching; and exposure risk to potentially infectious blood and/or body fluids, fumes or chemicals. CRC 1 will be delegated tasks by the Clinical Research Coordinator 2 or Supervisor.

There will be times when an adjustment in work hours, to include weekends, is necessary. The Clinical Research Coordinator 1 will be the secondary contact for the study subjects.

The Clinical Research Coordinator 1 is responsible for communicating problems, questions and/or clarifications. These communications can include, but are not limited to, protocol clarifications, protocol deviations and adverse event reporting. The Clinical Research Coordinator 1 will communicate all problems, questions and/or clarifications to the CRC 2, CRC Supervisor and/or Clinical Study Manager for their direct communication with the Sponsor.

OTHER SKILLS AND ABILITIES:

Excellent written and oral communication skills.
Ability to understand complex written and oral instructions.
Basic computer knowledge and applications required for generation of business correspondence and preparation of regulatory and other study documents.
Strong interpersonal skills.
Excellent attention to detail.
Exceptional organizational skills.
Ability to set and meet deadlines with high quality work.
Knowledge of the clinical research process, including Good Clinical Practices, informed consent process, drug accountability procedures, and IRB submission and reporting.
Possible equipment includes, but is not limited to computers, rolling carts, fax machine, photocopier, telephone, lab apparatus, needles, spirometry, centrifuges, allergy testing equipment, scales, microscope, calculators, vital signs equipment, and ECG machines.

REQUIREMENTS:

Required: Bachelor’s Degree (preferably in the field of Life Sciences or Health) or 1-2 years of clinical research experience.
Required: At least 18 months experience as a Assistant Clinical Research Coordinator

Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility, and ability to work independently.

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.

The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):

United States of America - $24.04 - $47.60

The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide ! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn .

Apply Now

Refine Your Search

clinical research coordinator jobs in san antonio, tx

Clinical Research Coordinator 1

Clinical Research Coordinator I - MTBI2

Clinical Research Coordinator

Clinical Research Coordinator Assistant

Clinical Research Coordinator

CTO Clinical Research Coordinator-Associate (Mays Cancer Center)

Clinical Research Coordinator

Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Data Coordinator I (CS3622 - Hamilton Wolfe)

Clinical Research Coordinator

CTO Clinical Research Coordinator-Associate (Mays Cancer Center)

Clinical Research Assistant

Research Coordinator

Clinical Coordinator Float

Clinical Coordinator

Clinical Nurse Coordinator Med Surg Oncology

Clinical Nurse Coordinator Med Surg ICU

Clinical Nurse Coordinator Lung Rescue ICU

I want to receive the latest job alert for clinical research coordinator in san antonio, tx

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