Lexington, MA · On-site
Clinical Trial Insurance, IWRS specs, Lab Manual, Licensing Agreements etc.) Provides oversight of Clinical CRO Investigator background checks. Assists in oversight of vendor shipment of clinical ...
Lexington, MA · On-site
Clinical Trial Insurance, IWRS specs, Lab Manual, Licensing Agreements etc.) Provides oversight of Clinical CRO Investigator background checks. Assists in oversight of vendor shipment of clinical ...
Lexington, MA · On-site
Provides oversight of Clinical CRO Investigator background checks. * Assists in oversight of vendor shipment of clinical supplies (e.g. lab kits, test machines, equipment etc.) being sent to sites ...
Lexington, MA · On-site
Provides oversight of Clinical CRO Investigator background checks. * Assists in oversight of vendor shipment of clinical supplies (e.g. lab kits, test machines, equipment etc.) being sent to sites ...
Lexington, MA · On-site
May assist in authoring/contributing to clinical study documents and study related plans developed by Clinical CRO and vendors. Responsibilities- Leads and/or assists the study team to execute the ...
Lexington, MA · On-site
May assist in authoring/contributing to clinical study documents and study related plans developed by Clinical CRO and vendors. Responsibilities- Leads and/or assists the study team to execute the ...
Watertown, MA · On-site
$153K - $197K/yr
Manage clinical CRO(s) and other study vendors from initial contact through to final study deliverables. * Lead external (CRO) trial management team, to ensure conduct in accordance with State and ...
Watertown, MA · On-site
$153K - $197K/yr
Manage clinical CRO(s) and other study vendors from initial contact through to final study deliverables. * Lead external (CRO) trial management team, to ensure conduct in accordance with State and ...
Watertown, MA · On-site
$153K - $197K/yr
Manage clinical CRO(s) and other study vendors from initial contact through to final study deliverables. * Lead external (CRO) trial management team, to ensure conduct in accordance with State and ...
Watertown, MA · On-site
$153K - $197K/yr
Manage clinical CRO(s) and other study vendors from initial contact through to final study deliverables. * Lead external (CRO) trial management team, to ensure conduct in accordance with State and ...
Experience in managing global clinical operations for first-in-human to Phase 3 Programs from start-up to close out, including managing clinical CRO and other vendors, budgets and timelines * In ...
Experience in managing global clinical operations for first-in-human to Phase 3 Programs from start-up to close out, including managing clinical CRO and other vendors, budgets and timelines * In ...
Experience in managing global clinical operations for first-in-human to Phase 3 Programs from start-up to close out, including managing clinical CRO and other vendors, budgets and timelines * In ...
Experience in managing global clinical operations for first-in-human to Phase 3 Programs from start-up to close out, including managing clinical CRO and other vendors, budgets and timelines * In ...
With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway, including formulation development ...
With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway, including formulation development ...
Katalyst CRO is seeking a Senior Clinical SAS Programmer who will represent the programming function in multi-disciplinary team meetings. The role involves developing CDISC-compliant datasets and ...
Katalyst CRO is seeking a Senior Clinical SAS Programmer who will represent the programming function in multi-disciplinary team meetings. The role involves developing CDISC-compliant datasets and ...
Clinical & Nonclinical CRO Oversight * Provide GCP/GLP quality oversight of CROs supporting clinical trials and nonclinical/toxicology studies to ensure all activities are conducted in strict ...
Clinical & Nonclinical CRO Oversight * Provide GCP/GLP quality oversight of CROs supporting clinical trials and nonclinical/toxicology studies to ensure all activities are conducted in strict ...
San Carlos, CA · Remote
$210K - $280K/yr
Clinical & Nonclinical CRO Oversight * Provide GCP/GLP quality oversight of CROs supporting clinical trials and nonclinical/toxicology studies to ensure all activities are conducted in strict ...
Quick apply
San Carlos, CA · Remote
$210K - $280K/yr
Clinical & Nonclinical CRO Oversight * Provide GCP/GLP quality oversight of CROs supporting clinical trials and nonclinical/toxicology studies to ensure all activities are conducted in strict ...
San Carlos, CA · On-site
$210K - $280K/yr
Clinical & Nonclinical CRO Oversight * Provide GCP/GLP quality oversight of CROs supporting clinical trials and nonclinical/toxicology studies to ensure all activities are conducted in strict ...
San Carlos, CA · On-site
$210K - $280K/yr
Clinical & Nonclinical CRO Oversight * Provide GCP/GLP quality oversight of CROs supporting clinical trials and nonclinical/toxicology studies to ensure all activities are conducted in strict ...
You enjoy working with a mid-sized CRO where you can build professional relationships with your colleagues at all levels * You bring previous experience in managing the clinical monitoring portion of ...
Quick apply
You enjoy working with a mid-sized CRO where you can build professional relationships with your colleagues at all levels * You bring previous experience in managing the clinical monitoring portion of ...
Princeton, NJ · On-site
Only Green Card or Citizens local to New Jersey 9-11 years of experience in a pharmaceutical company/CRO with business analyst along with project management Strong understanding/knowledge on clinical ...
Princeton, NJ · On-site
Only Green Card or Citizens local to New Jersey 9-11 years of experience in a pharmaceutical company/CRO with business analyst along with project management Strong understanding/knowledge on clinical ...
Whippany, NJ 07981 Alliance Management is part of the Pharma Clinical Operations organization and is based in Whippany, NJ. The function is responsible to ensure that studies outsourced to the CRO ...
Whippany, NJ 07981 Alliance Management is part of the Pharma Clinical Operations organization and is based in Whippany, NJ. The function is responsible to ensure that studies outsourced to the CRO ...
Whippany, NJ 07981 Alliance Management is part of the Pharma Clinical Operations organization and is based in Whippany, NJ. The function is responsible to ensure that studies outsourced to the CRO ...
Whippany, NJ 07981 Alliance Management is part of the Pharma Clinical Operations organization and is based in Whippany, NJ. The function is responsible to ensure that studies outsourced to the CRO ...
You enjoy working with a mid-sized CRO where you can build professional relationships with your colleagues at all levels * You bring previous experience in managing the clinical monitoring portion of ...
You enjoy working with a mid-sized CRO where you can build professional relationships with your colleagues at all levels * You bring previous experience in managing the clinical monitoring portion of ...
Clinical Trial Site Readiness & CRO Development Consultant Location: Southern California Work Arrangement: Remote / Hybrid with onsite support as needed Start: ASAP Schedule: Variable based on ...
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Clinical Trial Site Readiness & CRO Development Consultant Location: Southern California Work Arrangement: Remote / Hybrid with onsite support as needed Start: ASAP Schedule: Variable based on ...
Manhattan, NY · On-site
$200K - $225K/yr
Our team comprises seasoned clinical research professionals, data scientists, and AI experts ... They bring deep CRO domain knowledge and credibility, acting as a peer-level advisor to operational ...
Manhattan, NY · On-site
$200K - $225K/yr
Our team comprises seasoned clinical research professionals, data scientists, and AI experts ... They bring deep CRO domain knowledge and credibility, acting as a peer-level advisor to operational ...
Coordinate and manage the completion of the Clinical Laboratory Worksheet (CLW) and communicate information as required to other departments within ICON Laboratories (and ICON Clinical CRO if ...
Coordinate and manage the completion of the Clinical Laboratory Worksheet (CLW) and communicate information as required to other departments within ICON Laboratories (and ICON Clinical CRO if ...
$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
States with the most job openings for Clinical Cro jobs include:
For Clinical Cro jobs, the most frequently searched job titles are:
Full-time
Re-posted 2 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.
The in-house Clinical Research Associate (CRA) is responsible for providing support for day to day clinical study activities under general supervision of the the Clinical Project Manager(s).
The CRA also provides support for existing departmental tasks and may take on developmental tasks as appropriate upon discussions with manager.
The CRA performs work within established protocols under general supervision.
Assists the study team(s) to deliver the clinical study within agreed timelines.
Assists in authoring/contributing to clinical study documents and study related plans developed by Clinical CROs and vendors. (E.g. Clinical Trial Insurance, IWRS specs, Lab Manual, Licensing Agreements etc.) Provides oversight of Clinical CRO Investigator background checks.
Assists in oversight of vendor shipment of clinical supplies (e.g. lab kits, test machines, equipment etc.) being sent to sites prior to initiation as necessary.
Provides oversight of Essential Documents for Investigational Medicine Release as per relevant SOP.
Reviews Clinical Monitoring Reports and correspondence related to restudy and Initiation Visits and follows up with Clinical CRO to resolve open action items.
Manages escalation of study related issues and communicates as appropriate with Clinical Project Manager.
Responsible for the operational oversight of the Clinical CRO with regards to data feed setup in the Clinical Trial Management System.
Assists and/or participates in planning and conduct of Investigator's Meetings as necessary.
Assists Clinical Project Manager in tracking study related activities which are not appropriate to be outsourced.
Reviews a percentage of monitoring visit reports for oversight and escalates issues to Clinical Project Manager.
Assists with agenda distribution & minute taking for internal clinical study team meetings where formal documentation is needed and the Clinical CRO is not present.
Provides oversight of Clinical CRO activities regarding amendments to confidentiality and site agreements.
Assists study team with preparation for audits/inspections Reviews clinical close out monitoring visit reports for oversight and escalates issues to the Clinical Project Manager.
Liaises with Transparency group to ensure Clintrials.gov is updated.
Feel free to forward my email to your friends/colleagues who might be available.
Thanks,
Warm Regards,
Kavita Kumari
Integrated Resources, Inc.
Direct: (732) - 844 8725
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
