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Weekend Clinical Trial Transparency Jobs (NOW HIRING)

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$80K - $145K/yr

Sr Medical Writer, Redaction (Clinical Trial Transparency) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with ...

Position : Clinical Trial Assistant Location : Sparks, MD Duration : 12 Months Contract Shift ... with Transparency (Sunshine) Act reporting, either by gathering data or with data entry. Other ...

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and ... Responsible for management of vendors to support clinical trial execution * Plan, execute, and lead ...

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and ... Responsible for management of vendors to support clinical trial execution * Plan, execute, and lead ...

... transparency, and performance accountability. Within this model, the Clinical Trial Manager (CTM ... is the country-level owner of study delivery outcomes and the primary advocate for the client ...

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.

Clinical Trial Manager

Boston, MA · On-site

$133K - $157K/yr

Seaport Therapeutics is seeking a Clinical Trial Manager to join our Development team. The Clinical ... CNS therapeutic experience strongly preferred At Seaport, we believe transparency and fairness are ...

Clinical Trial Manager

Boston, MA · On-site

$133K - $157K/yr

Seaport Therapeutics is seeking a Clinical Trial Manager to join our Development team. The Clinical ... CNS therapeutic experience strongly preferred At Seaport, we believe transparency and fairness are ...

Clinical Operations Associate (Pool)

CA · Remote

$70K - $80K/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 ...

Responsible for determining if a study is a qualifying clinical trial, and performing the initial ... Monday - Friday Weekend Requirements: None Benefits: Yes Unions: No Position Status: Exempt Weekly ...

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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 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.
More about Weekend Clinical Trial Transparency jobs
What cities are hiring for Weekend Clinical Trial Transparency jobs? Cities with the most Weekend Clinical Trial Transparency job openings:
What are the most commonly searched types of Clinical Trial Transparency jobs? The most popular types of Clinical Trial Transparency jobs are:
What states have the most Weekend Clinical Trial Transparency jobs? States with the most job openings for Weekend Clinical Trial Transparency jobs include:
What job categories do people searching Weekend Clinical Trial Transparency jobs look for? The top searched job categories for Weekend Clinical Trial Transparency jobs are:
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.
Clinical Trial Transparency Senior Associate

Clinical Trial Transparency Senior Associate

Integrated Resources INC

Cambridge, MA

$36.50 - $50/hr

Other

Medical, Life

Posted 12 days 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

Job Title: Clinical Trial Transparency Senior Associate

Location: Cambridge, MA
Duration: 7+ months (Possibility of extension)
Job Description:
Performs the Clinical Trial Registration and/or results disclosure activities for new and/or ongoing studies.
Ensures compliance due dates are defined and timelines are met.
Collaborates with the Study Team to complete the data entry in support of Clinical Trial Disclosure, utilizing information from source documents and systems (e.g. protocol, CTMS).
Assigns tasks, initiates workflows, follows up on all action required, and escalates alerts when needed in order to maintain content that has been made public (e.g. clinicaltrials.gov).
Shares accurate information with various functional leads to be utilized throughout global disclosures
Performs internal quality control review of disclosure information.
Participates in User-Acceptance Testing (UAT) of disclosure system.
Supports process analysis efforts by identifying opportunities to improve the efficiency and effectiveness of the Clinical Trial Disclosure process.
Generates metrics for disclosure activities.
Supports the development and delivery of training materials.
Requirements:
Firm understanding of Clinical Development and operations.
Previous experience (2-3 years minimum) in pharma/biotech industry.
Must have previous experience disclosing clinical trial information on ClinicalTrials.gov.
Minimum education of Bachelor Degree (or equivalent experience).
Experience with PharmaCM would be a plus.


Additional Information

We do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job.

Thanks & Regards,


Seema Chawhan
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I

DIRECT # - 732-844-8724|


LinkedIn: https://in.linkedin.com/in/seemachawhan
Gold Seal JCAHO Certified  for Health Care Staffing
"INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row)


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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