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Weekend Clinical Trial Transparency Jobs (NOW HIRING)

Skyhawk Therapeutics

Clinical Trial Associate

Waltham, MA · On-site

$75K - $140K/yr

Skyhawk Therapeutics is committed to pay transparency and equitable compensation practices. The base salary range for the Clinical Trial Associate is $75,000-140,000 annually. This range reflects the ...

Ipsen

Clinical Trial Administrator

Cambridge, MA

Clinical Trial Administrator Company: Ipsen Biopharmaceuticals Inc. About Ipsen: Ipsen is a mid ... When needed, liaise with the Local Transparency Manager (LTM) or the Global Transparency Manager.

Seaport Therapeutics

Clinical Trial Manager

Boston, MA · On-site

$133K - $150K/yr

The Clinical Trial Manager (CTM) is responsible for leading the execution of clinical studies on ... CNS therapeutic experience strongly preferred At Seaport, we believe transparency and fairness are ...

Seaport Therapeutics

Clinical Trial Manager

Boston, MA · On-site

$133K - $150K/yr

The Clinical Trial Manager (CTM) is responsible for leading the execution of clinical studies on ... CNS therapeutic experience strongly preferred At Seaport, we believe transparency and fairness are ...

Innovo Research

Clinical Trial Recruiter

Champaign, IL · On-site

$19.25/hr

Vision Insurance COMPENSATION In the spirit of transparency, we are pleased to announce that the ... Occasional evening and weekend work may be required as job duties demand. The above statements are ...

A-Line Staffing Solutions

Be Seen First

Clinical Trial Operations Specialist

Irvine, CA · On-site

$35 - $40/hr

... transparency reporting data to support Sunshine Act compliance. · Track, manage, and coordinate ... Clinical Trial Operations Specialist Requirements * Previous clinical trial experience is required.

Socket.dev

Clinical Trial Associate

Waltham, MA · On-site

$65 - $90/hr

We are seeking a Clinical Trial Associate (CTA) will work with the Clinical Study Lead and Director ... Additional Description for Pay Transparency: The final salary offered will depend on several ...

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Weekend Clinical Trial Transparency information

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

As of Sep 5, 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.

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.
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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 August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Associate

Skyhawk Therapeutics

Waltham, MA • On-site

$75K - $140K/yr

Full-time

Re-posted 14 days ago

Job description

Clinical Trial Associate/ Senior Clinical Trial Associate
Skyhawk Therapeutics is seeking a highly motivated CTA to provide administrative and operational support to Clinical Operations.
Responsibilities (including, but not limited to):
  • Organize, participate in, and maintain agendas and meeting minutes for all internal and cross-functional team meetings. Review external meeting minutes as required.
  • Work closely with our clinical operations team to coordinate, track, and manage logistics in support of studies (e.g. review study plans, assist with eTMF reviews).
  • Update and maintain internal trackers (e.g. central enrollment tracker, investigator engagement tracker, bioanalytical sample tracker) and implement updates into ad-hoc presentations and reports as required.
  • Maintain internal Clinical Operations study files and perform periodic reconciliations of documents to ensure all material is present and versioned correctly.
  • Create and maintain study personnel contact lists for all studies and KOLs by disease indication.
  • Assist with the review of study-related documents for clinical studies (e.g. protocol, IB, ICFs).
  • Assist with the facilitation of important external meetings (e.g. Clinical Advisory Board meetings): outreach, scheduling, execution of CDAs and contracts, travel arrangements, presentations, agendas, and minutes.
  • Assist with bioanalytical sample tracking and management of central and third-party labs (sample shipment and analysis timelines).
  • Assist with the review of central and third-party lab documents (e.g. Lab Manual, site flowcharts).
  • Assist with monitoring trip report across the program.

Requirements, Education, Experience & Skills:
  • Relevant education and training required; Bachelor's degree in administrative, science or medical areas of study is a plus.
  • At least 3-5 years of successful administrative experience in biotech/life sciences, health care or clinical study management (title commensurate with experience, with emphasis on eTMF experience)
  • Prefers to contribute as both independent, self-starter, and a collaborative team member.
  • Excellent organizational skills; prefers and can adapt to multiple priorities in a fast-paced and fluid work environment.
  • Excellent verbal and written communication skills.
  • Excellent computer skills, including Microsoft Office Suite: Calendar, Word, Excel, and PowerPoint are essential. SharePoint and SmartSheet preferred.
  • Veeva TMF working knowledge and for senior level, demonstrated knowledge of ICH-GCP, FDA and international regulatory requirements, eTMF management/oversight, and inspection readiness
  • Demonstrated multi-tasking and project management skills.

Skyhawk Therapeutics is committed to pay transparency and equitable compensation practices. The base salary range for the Clinical Trial Associate is $75,000-140,000 annually. This range reflects the minimum and maximum target for such position. Skyhawk Therapeutics will assess the appropriate level for a qualified candidate based on job-related skills, professional experience, and relevant education or training.
About Skyhawk
Skyhawk is committed to discovering, developing and commercializing small molecule therapeutics that modify RNA expression. We use our novel SkySTAR® platform (Skyhawk Small molecule Therapeutics for Alternative splicing of RNA) to develop drug candidates directed toward targets for some of the world's most intractable diseases including neurological conditions, cancer, and traditionally "undruggable" targets.

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