ZipRecruiter

Log In

1

Weekend Clinical Trial Transparency Jobs in Texas

Adams Clinical

Lead Dosing Session Monitor

Dallas, TX

$60 - $70/hr

Join Us in Shaping the Future of Clinical Research   Adams Clinical is a leading clinical trial ... A culture of respect, transparency, and continuous improvement  * Opportunities for professional ...

Adams Clinical

Lead Dosing Session Monitor

Dallas, TX · On-site

$60 - $70/hr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... A culture of respect, transparency, and continuous improvement * Opportunities for professional ...

Adams Clinical

Lead Dosing Session Monitor

Dallas, TX

$60 - $70/hr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... A culture of respect, transparency, and continuous improvement * Opportunities for professional ...

Adams Clinical

Clinical Research Assistant

Desoto, TX

$19.23 - $23.08/hr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... A culture of respect, transparency, and continuous improvement * Opportunities for professional ...

Adams Clinical

Clinical Research Assistant

Desoto, TX · On-site

$19.23 - $23.08/hr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... A culture of respect, transparency, and continuous improvement * Opportunities for professional ...

next page

Showing results 1-20

All JobsClinical Trial Transparency JobsWeekend Clinical Trial Transparency JobsWeekend Clinical Trial Transparency Jobs in Texas

Weekend Clinical Trial Transparency information

What is a weekend clinical trial transparency role?

A Weekend Clinical Trial Transparency role involves ensuring that clinical trial data and results are accurately and ethically disclosed to the public, often by managing documentation, reporting, and compliance with regulatory requirements over the weekend. Professionals in this role work to maintain transparency in clinical research by preparing trial summaries, updating clinical trial registries, and responding to disclosure queries. This helps uphold ethical standards, increases public trust, and supports regulatory compliance. Weekend positions are often needed to provide continuous support, address urgent requests, and meet tight submission deadlines.

What are the key skills and qualifications needed to thrive as a weekend clinical trial transparency specialist?

To excel as a Weekend Clinical Trial Transparency Specialist, you need a solid understanding of clinical research protocols, regulatory requirements, and strong attention to detail, often supported by a background in life sciences or related fields. Familiarity with clinical trial registries (such as ClinicalTrials.gov), data management systems, and relevant compliance frameworks is essential. Strong organizational skills, effective written communication, and the ability to work independently are standout soft skills in this role. These competencies ensure accurate, timely, and compliant disclosure of clinical trial information, which is critical for regulatory adherence and public trust.

How does working in a weekend clinical trial transparency role differ from weekday positions, and what should applicants expect regarding work-life balance?

Weekend Clinical Trial Transparency roles often require ensuring that clinical trial data is accurately disclosed and compliant with regulatory standards during non-standard business hours. Applicants can expect to work independently or with a small weekend team, communicating remotely with weekday staff as needed. While weekend shifts can offer flexibility and potentially less overlap with meetings, the role may involve resolving urgent disclosure issues or assisting with last-minute updates to trial registries. Maintaining clear documentation and proactive communication with the broader team are key for success and continuity across shifts.

What are the most commonly searched types of Clinical Trial Transparency jobs in Texas?

The most popular types of Clinical Trial Transparency jobs in Texas are:

What are popular job titles related to Weekend Clinical Trial Transparency jobs in Texas?

For Weekend Clinical Trial Transparency jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Weekend Clinical Trial Transparency jobs in Texas look for?

The top searched job categories for Weekend Clinical Trial Transparency jobs in Texas are:

Weekend Clinical Trial Transparency jobs near you
Infographic showing various Weekend Clinical Trial Transparency job openings in Texas as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 18% Part Time, and 6% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.

Clinical Trial Research Assistant

Advanced Rheumatology of Houston

The Woodlands, TX • On-site

$15 - $18/hr

Full-time

Re-posted 3 days ago

Job description

Clinical Trial Research Assistant
The Woodlands, TX | Full-Time | Private Outpatient Medical Clinic/Onsite

Woodlands Private Outpatient Medical Clinic is actively seeking a Clinical Trial Research Assistant to join our dedicated clinical research team. This is an exciting opportunity to be involved in cutting-edge medical research in a supportive and dynamic outpatient setting.

Key Responsibilities:
  • Process and ship biological specimens per study protocol.
  • Maintain lab inventory and order clinical trial supplies.
  • Ensure accurate and complete study documentation in compliance with institutional and federal regulations.
  • Support research coordinators with testing procedures and overall trial conduct.
  • Advertise, screen, recruit, and enroll patients in clinical trials.
  • Obtain informed consent and explain study participation clearly.
  • Schedule appointments, diagnostic tests, and study-related procedures.
  • Assist with data entry into electronic case report forms (eCRFs) and databases.
  • Support the preparation and submission of reports to regulatory bodies (IRB, FDA, DSMB).
  • Maintain knowledge of current study protocols and standard operating procedures.
  • Prepare for monitoring visits, sponsor audits, and regulatory inspections.
  • Help collect and report adverse events.
  • Attend ongoing training and continuing education relevant to research duties.

Preferred Skills:
  • Phlebotomy, ECG/EKG, and vital signs collection preferred (or willingness to be trained).
  • Experience with specimen processing, shipping, and documentation.
  • Bilingual (English/Spanish) is a plus.

Requirements:
  • Bachelor’s degree preferred; however, candidates with a strong work history and medical office experience will also be considered.
  • Previous lab experience with biological specimen handling.
  • Proficient in maintaining documentation and adhering to study protocols.
  • MUST live within 30 mins of The Woodlands.
  • THIS POSITION IS ONSITE.
  • Must be Technologically Adept.
  • Strong attention to detail and protocol compliance.
  • Excellent communication and organizational skills.

Why Join Us?
  • Supportive, collaborative team environment.
  • Opportunity to work on innovative, impactful clinical trials.
  • On-the-job training and professional development.
  • Regular weekday schedule with no night or weekend shifts.