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Weekend Clinical Trial Transparency Jobs (NOW HIRING)

Biogen

Sr. Manager - Clinical Trial Lead

Cambridge, MA · On-site

... transparency, regularly monitoring the budget to identify potential overspending and addressing ... department clinical trial outsourcing models; provides feedback via appropriate channels for ...

AstraZeneca

Local Study Associate Director

Wilmington, DE · On-site

$32.50 - $44.50/hr

Ensure set-up, updating and access to business-critical systems for Safety Reporting, Regulatory Submissions and Clinical Trial Transparency at country level. Ensure accuracy and compliance of all ...

Vanguard Clinical

Clinical Research Associate (Pool)

CA · Remote

$90K - $130K/yr

Our mission is to bring innovation to clinical trial execution through passion, transparency, co-active communication, and integrity, to facilitate the successful development of life-changing ...

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How much do weekend clinical trial transparency jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for weekend clinical trial transparency in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

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.

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 key skills and qualifications needed to thrive as a Weekend Clinical Trial Transparency Specialist, and why are they important?

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.
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Weekend Clinical Trial Transparency jobs near you
Infographic showing various Weekend Clinical Trial Transparency job openings in the United States as of May 2026, with employment types broken down into 50% As Needed, and 50% Full Time. Highlights an 75% Physical, 5% Hybrid, and 20% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.
Regulatory Compliance Coordinator

Regulatory Compliance Coordinator

Integrated Resources INC

Woodcliff Lake, NJ

Full-time

Posted 19 hours ago

Job description

Company Description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

"Work across multiple disciplines within and outside Regulatory Affairs to drive departmental and project objectives. 

Responsibilities:

  • Person will be responsible for coordinating the posting of registration and disclosures on clinicaltrials.gov, EudraCT and other registries for company-wide studies. This comprises supervision of the vendor as well as coordination of company internal processes to ensure compliance with all relevant legal obligations (primarily clinicaltrials.gov and EudraCT disclosure). 
  • Database proficient with registrations and disclosures preferred. 
  • Has the ability to work cross-functionally and meet required deadlines. 
  • Ensures trial disclosure is in compliance with applicable regulations globally. 
  • Develops and maintains strong internal relationships across all levels of the clinical organization. 
  • Escalates issues to management in an expedient manner. 
  • Continually train and remain in compliance with all current industry requirements as they relate to clinical trial disclosures. 
  • Reviews of clinical and regulatory documents and regulatory submissions for data accuracy, consistency, formal quality and readability, resolving identified issues in collaboration with authors in a productive fashion 
  • Coordinates all clinical disclosure activities, acting as primary intermediary between the disclosure vendor and contacts 30 
  • Works with contacts to identify and resolve compliance gaps 30 Supports continual improvements by evaluating disclosure business process, suggests and implements improvements to enhance compliance, documents processes and trains relevant personnel 20 
  • Maintains disclosure trackers and produces metrics reports for management 10 
  • Maintains product information for use in disclosure activities 10 
Qualifications

Requirements:

  • Bachelor's degree required 
  • At least 3 years working in the pharmaceutical industry in an R&D environment. 
  • Solid knowledge of clinical trial transparency principles, preferably on an international level 
  • Strong attention to detail and the ability to work as a part of a team across multiple departments 
  • Strong communication and influencing skills "
Additional Information

Feel free to forward my email to your friends/colleagues who might be available. We do offer referral bonus


Kind Regards,

Neomi Nieves
Clinical Recruiter
Integrated Resources, Inc
IT REHAB CLINICAL NURSING
Inc. 5000 | 2007 - 2014
Main: 732-549-2030 x140
Direct: 732-902-2064
Website: www.irionline.com


Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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