$36.50 - $50/hr
Clinical Trial Transparency Senior Associate Location: Cambridge, MA Duration: 7+ months (Possibility of extension) : Performs the Clinical Trial Registration and/or results disclosure activities for ...
$36.50 - $50/hr
Clinical Trial Transparency Senior Associate Location: Cambridge, MA Duration: 7+ months (Possibility of extension) : Performs the Clinical Trial Registration and/or results disclosure activities for ...
Woodcliff Lake, NJ · On-site
$35.50 - $48.50/hr
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 ...
Woodcliff Lake, NJ · On-site
$35.50 - $48.50/hr
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 ...
$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 ...
$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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
Ensure company compliance with clinical trial transparency laws and requirements by applying expert knowledge of key regulatory frameworks, including FDAA 801 and Final Rule and CTR 536/2014. * Work ...
Ensure company compliance with clinical trial transparency laws and requirements by applying expert knowledge of key regulatory frameworks, including FDAA 801 and Final Rule and CTR 536/2014. * Work ...
Sparks, MD · On-site
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 ...
Sparks, MD · On-site
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 ...
$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 ...
$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 ...
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 ...
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 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 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.
... 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 ...
... 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 ...
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 ...
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 ...
$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 ...
$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 ...
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 ...
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 ...
Foster City, CA · On-site +1
CLINICAL TRIAL DISCLOSURE & TRANSPARENCY: The Disclosure &Transparency function resides organizationally within Medical Writing The Disclosures function is responsible for clinical trial ...
Foster City, CA · On-site +1
CLINICAL TRIAL DISCLOSURE & TRANSPARENCY: The Disclosure &Transparency function resides organizationally within Medical Writing The Disclosures function is responsible for clinical trial ...
The incumbent will build and lead systems that promote transparency, accountability, and efficiency ... Supervise clinical trial operations staff, ensuring alignment with MCW's mission, policies, and NIH ...
The incumbent will build and lead systems that promote transparency, accountability, and efficiency ... Supervise clinical trial operations staff, ensuring alignment with MCW's mission, policies, and NIH ...
The incumbent will build and lead systems that promote transparency, accountability, and efficiency ... Supervise clinical trial operations staff, ensuring alignment with MCW's mission, policies, and NIH ...
The incumbent will build and lead systems that promote transparency, accountability, and efficiency ... Supervise clinical trial operations staff, ensuring alignment with MCW's mission, policies, and NIH ...
Solid knowledge of clinical trial transparency principles, preferably on an international leve Strong attention to detail and the ability to work as a part of a team across multiple departments ...
Solid knowledge of clinical trial transparency principles, preferably on an international leve Strong attention to detail and the ability to work as a part of a team across multiple departments ...
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
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
$28.85 - $34.97
4% of jobs
$34.97 - $41.08
6% of jobs
$41.08 - $47.20
7% of jobs
$51.79 is the 25th percentile. Wages below this are outliers.
$47.20 - $53.32
9% of jobs
$53.32 - $59.44
15% of jobs
The median wage is $62.14 / hr.
$59.44 - $65.56
18% of jobs
$69.92 is the 75th percentile. Wages above this are outliers.
$65.56 - $71.68
21% of jobs
$71.68 - $77.80
7% of jobs
$77.80 - $83.92
6% of jobs
$83.92 - $90.03
3% of jobs
$90.03 - $96.15
2% of jobs
$28
$62
$96
A Clinical Trial Transparency job involves ensuring that information about clinical trials is publicly disclosed in compliance with global regulations and transparency policies. Professionals in this role manage the registration of trials on public databases, oversee the timely reporting of results, and ensure adherence to ethical and legal requirements. They collaborate with regulatory teams, medical writers, and legal departments to promote data accessibility and public trust in clinical research.
In a Clinical Trial Transparency role, your primary responsibilities include preparing and submitting clinical trial data and documents to public registries, ensuring compliance with global regulations, and responding to transparency-related inquiries from regulatory authorities. You’ll work closely with clinical teams, regulatory affairs, and medical writing staff to gather accurate data and ensure timely disclosures. The role often involves managing multiple projects simultaneously, staying updated on evolving disclosure regulations, and supporting audits or inspections. This position is essential in promoting openness, protecting patient privacy, and maintaining the integrity of clinical research.
Excelling in Clinical Trial Transparency requires a comprehensive understanding of clinical research protocols, regulatory compliance (such as FDA, EMA, and ICMJE requirements), and strong project management abilities. Familiarity with disclosure platforms (e.g., ClinicalTrials.gov, EudraCT), data anonymization tools, and relevant certifications like a GCP (Good Clinical Practice) certificate are highly valuable. Attention to detail, effective communication, and stakeholder management are crucial soft skills for success in this role. These capabilities ensure accurate, timely, and compliant disclosure of trial information, which is critical for regulatory approval and upholding public trust.
$36.50 - $50/hr
Other
Medical, Life
Posted 16 days ago
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 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.
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 MBEÂ |GSA - Schedule 66Â IÂ GSA - Schedule 621I
DIRECT # -Â 732-844-8724|
LinkedIn:Â 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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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.
Recruiting and staffing services
51 - 200 Employees
Edison, NJ, US
1996
