Cambridge, MA · On-site
$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 ...
Cambridge, MA · On-site
$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 ...
Blue Bell, PA · On-site
Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards. * Foster strong relationships with study sites and investigators to enhance patient recruitment ...
Blue Bell, PA · On-site
Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards. * Foster strong relationships with study sites and investigators to enhance patient recruitment ...
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 ...
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 ...
Blue Bell, PA · On-site +1
Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards. * Foster strong relationships with study sites and investigators to enhance patient recruitment ...
Blue Bell, PA · On-site +1
Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards. * Foster strong relationships with study sites and investigators to enhance patient recruitment ...
Blue Bell, PA · On-site
Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards. * Foster strong relationships with study sites and investigators to enhance patient recruitment ...
Blue Bell, PA · On-site
Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards. * Foster strong relationships with study sites and investigators to enhance patient recruitment ...
Tomball, TX · On-site
$50 - $70/hr
Clinical Trial Screening Coordinator Location: Tomball, TX Job Id: 1102 # of Openings: 1 Clinical ... Accountable for coordinating pre-screen data management activities - performing quality checks on ...
Tomball, TX · On-site
$50 - $70/hr
Clinical Trial Screening Coordinator Location: Tomball, TX Job Id: 1102 # of Openings: 1 Clinical ... 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 ...
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 ...
Atlanta, GA · On-site
$23.25 - $31/hr
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 in a timely ...
Atlanta, GA · On-site
$23.25 - $31/hr
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 in a timely ...
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 ...
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 ...
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 ...
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 ...
Lakewood, CO · On-site
$43K - $54K/yr
Accurately input clinical trial data into clinical data management systems (CDMS) or case report forms (CRFs), rigorously verifying it against source documentation. * Ensure all data entry activities ...
Lakewood, CO · On-site
$43K - $54K/yr
Accurately input clinical trial data into clinical data management systems (CDMS) or case report forms (CRFs), rigorously verifying it against source documentation. * Ensure all data entry activities ...
Atlanta, GA · On-site
$65 - $90/hr
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 in a timely ...
Atlanta, GA · On-site
$65 - $90/hr
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 in a timely ...
Salt Lake City, UT · On-site
$28K - $70K/yr
... P1 - Entry Level Pro FLSA Code Administrative Patient Sensitive Job Code? No Standard Hours per ... Compile, analyze, clean, and validate clinical trial data. Identify and resolve discrepancies and ...
Salt Lake City, UT · On-site
$28K - $70K/yr
... P1 - Entry Level Pro FLSA Code Administrative Patient Sensitive Job Code? No Standard Hours per ... Compile, analyze, clean, and validate clinical trial data. Identify and resolve discrepancies and ...
$27K - $62K/mo
... P1 - Entry Level Pro FLSA Code Administrative Patient Sensitive Job Code? No Standard Hours per ... Compile, analyze, clean, and validate clinical trial data. Identify and resolve discrepancies and ...
$27K - $62K/mo
... P1 - Entry Level Pro FLSA Code Administrative Patient Sensitive Job Code? No Standard Hours per ... Compile, analyze, clean, and validate clinical trial data. Identify and resolve discrepancies and ...
$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 ...
$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 ...
Duarte, CA · On-site
Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout. * Ensure data accuracy, completeness ...
Duarte, CA · On-site
Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout. * Ensure data accuracy, completeness ...
$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
6% of jobs
$47.05 - $53.67
3% of jobs
$53.67 - $60.29
2% of jobs
$60.29 - $66.91
0% of jobs
$66.91 - $73.54
0% of jobs
$73.54 - $80.16
1% of jobs
$80.16 - $86.78
3% of jobs
$13
$38
$86
The most popular types of Clinical Trial Data Transparency jobs are:
$36.50 - $50/hr
Full-time
Medical, Life
Re-posted 11 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 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)
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.
Recruiting and staffing services
51 - 200 Employees
Edison, NJ, US
1996
