$36.50 - $50/hr
Clinical Trial Transparency Senior Associate Location: Cambridge, MA Duration: 7+ months ... Collaborates with the Study Team to complete the data entry in support of Clinical Trial Disclosure ...
$36.50 - $50/hr
Clinical Trial Transparency Senior Associate Location: Cambridge, MA Duration: 7+ months ... Collaborates with the Study Team to complete the data entry in support of Clinical Trial Disclosure ...
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 ...
Cambridge, MA · On-site
Clinical Trial Administrator Company: Ipsen Biopharmaceuticals Inc. About Ipsen: Ipsen is a mid ... Ensure the information is properly recorded in the Data Transparency system (COLLECT), implement ...
Cambridge, MA · On-site
Clinical Trial Administrator Company: Ipsen Biopharmaceuticals Inc. About Ipsen: Ipsen is a mid ... Ensure the information is properly recorded in the Data Transparency system (COLLECT), implement ...
Minnetonka, MN · On-site
Responsibilities include document management, data entry, communication with sites and vendors, and ... Maintain, organize, and update clinical trial documentation, including trial master files ...
Minnetonka, MN · On-site
Responsibilities include document management, data entry, communication with sites and vendors, and ... Maintain, organize, and update clinical trial documentation, including trial master files ...
Responsibilities include document management, data entry, communication with sites and vendors, and ... Maintain, organize, and update clinical trial documentation, including trial master files ...
Responsibilities include document management, data entry, communication with sites and vendors, and ... Maintain, organize, and update clinical trial documentation, including trial master files ...
Participate in clinical trial data management process. Conduct data analysis, visualization and data modeling based on report design in clinical data models including ambulatory, laboratory ...
Participate in clinical trial data management process. Conduct data analysis, visualization and data modeling based on report design in clinical data models including ambulatory, laboratory ...
Hillsborough, NJ · On-site
Participate in clinical trial data management process. Conduct data analysis, visualization and data modeling based on report design in clinical data models including ambulatory, laboratory ...
Hillsborough, NJ · On-site
Participate in clinical trial data management process. Conduct data analysis, visualization and data modeling based on report design in clinical data models including ambulatory, laboratory ...
San Jose, CA · On-site
In this role, you will support the integrity, quality, and timely delivery of clinical trial data from external sources, contributing directly to studies that improve patient outcomes worldwide. What ...
San Jose, CA · On-site
In this role, you will support the integrity, quality, and timely delivery of clinical trial data from external sources, contributing directly to studies that improve patient outcomes worldwide. What ...
Manage clinical trial data sets, ensuring accuracy, consistency, and security. Ensure that all clinical trial data are accurately entered into electronic data capture (EDC) systems and promptly ...
Manage clinical trial data sets, ensuring accuracy, consistency, and security. Ensure that all clinical trial data are accurately entered into electronic data capture (EDC) systems and promptly ...
Collaborate with Medical Lead/BSL to identify and safety trends; and as needed, reports on trial data to safety and clinical boards (e.g. SMT,GCT and GPT) In collaboration with Medical Lead/BSL or ...
Collaborate with Medical Lead/BSL to identify and safety trends; and as needed, reports on trial data to safety and clinical boards (e.g. SMT,GCT and GPT) In collaboration with Medical Lead/BSL or ...
East Hanover, NJ · On-site
Collaborate with Medical Lead/BSL to identify and safety trends; and as needed, reports on trial data to safety and clinical boards (e.g. SMT,GCT and GPT) In collaboration with Medical Lead/BSL or ...
East Hanover, NJ · On-site
Collaborate with Medical Lead/BSL to identify and safety trends; and as needed, reports on trial data to safety and clinical boards (e.g. SMT,GCT and GPT) In collaboration with Medical Lead/BSL or ...
East Hanover, NJ · On-site
With support, liaise with the trial data manager (TDM) and labs for data transfer and data ... At least 2 years of experience handling clinical samples Familiarity with biomarker discovery ...
East Hanover, NJ · On-site
With support, liaise with the trial data manager (TDM) and labs for data transfer and data ... At least 2 years of experience handling clinical samples Familiarity with biomarker discovery ...
Clinical Trial Screening Coordinator The Clinical Trial Screening Coordinator will act as a liaison ... Accountable for coordinating pre-screen data management activities - performing quality checks on ...
Clinical Trial Screening Coordinator The Clinical Trial Screening Coordinator will act as a liaison ... Accountable for coordinating pre-screen data management activities - performing quality checks on ...
Clinical Trial Screening Coordinator The Clinical Trial Screening Coordinator will act as a liaison ... Accountable for coordinating pre-screen data management activities - performing quality checks on ...
Clinical Trial Screening Coordinator The Clinical Trial Screening Coordinator will act as a liaison ... Accountable for coordinating pre-screen data management activities - performing quality checks on ...
New York, NY · On-site
$75K - $85K/yr
Track Case Report Forms, data queries, and clinical data flow from submission through resolution ... Coordinate with Clinical Trial Supply vendors and manage tracking systems for investigational ...
New York, NY · On-site
$75K - $85K/yr
Track Case Report Forms, data queries, and clinical data flow from submission through resolution ... Coordinate with Clinical Trial Supply vendors and manage tracking systems for investigational ...
Somerset, NJ · On-site
$60K - $75K/yr
The Clinical Data Manager ensures the integrity, accuracy, and compliance of clinical trial data, adhering to regulatory requirements, SOPs, and data standards. Responsibilities include overseeing ...
Somerset, NJ · On-site
$60K - $75K/yr
The Clinical Data Manager ensures the integrity, accuracy, and compliance of clinical trial data, adhering to regulatory requirements, SOPs, and data standards. Responsibilities include overseeing ...
Somerset, NJ · On-site
$60K - $75K/yr
The Clinical Data Manager ensures the integrity, accuracy, and compliance of clinical trial data, adhering to regulatory requirements, SOPs, and data standards. Responsibilities include overseeing ...
Somerset, NJ · On-site
$60K - $75K/yr
The Clinical Data Manager ensures the integrity, accuracy, and compliance of clinical trial data, adhering to regulatory requirements, SOPs, and data standards. Responsibilities include overseeing ...
Woodcliff Lake, NJ · On-site
$35.50 - $48.50/hr
... data accuracy, consistency, formal quality and readability, resolving identified issues in ... Solid knowledge of clinical trial transparency principles, preferably on an international level ...
Woodcliff Lake, NJ · On-site
$35.50 - $48.50/hr
... data accuracy, consistency, formal quality and readability, resolving identified issues in ... Solid knowledge of clinical trial transparency principles, preferably on an international level ...
Pittsburgh, PA · On-site
$32.50 - $44.50/hr
Conducting reviews of trial data and follow GCP/ICH protocols/guidelines. Will require travel to Clinical sites, including up to 50% of the time, during peak periods. Primary Responsibilities:
Pittsburgh, PA · On-site
$32.50 - $44.50/hr
Conducting reviews of trial data and follow GCP/ICH protocols/guidelines. Will require travel to Clinical sites, including up to 50% of the time, during peak periods. Primary Responsibilities:
Responsible for visualizing clinical trial data in SPOTFIRE for the Analytical Risk-based Monitoring (ARBM) group and for the medical reviewers in the iDARTs application (an internally developed tool ...
Responsible for visualizing clinical trial data in SPOTFIRE for the Analytical Risk-based Monitoring (ARBM) group and for the medical reviewers in the iDARTs application (an internally developed tool ...
$13.94 - $20.56
5% of jobs
$20.56 - $27.19
6% of jobs
$29.74 is the 25th percentile. Wages below this are outliers.
$27.19 - $33.81
35% of jobs
The median wage is $34.45 / hr.
$33.81 - $40.43
38% of jobs
$40.43 - $47.05
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$47.05 - $53.67
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$53.67 - $60.29
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$66.91 - $73.54
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$73.54 - $80.16
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$13
$38
$86
$36.50 - $50/hr
Other
Medical, Life
Posted 13 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
