Wilmington, DE · On-site
$87K - $145K/yr
Manage the progress of assigned studies by tracking regulatory submissions and approvals ... IQVIA is a leading global provider of clinical research services, commercial insights and health ...
Wilmington, DE · On-site
$87K - $145K/yr
Manage the progress of assigned studies by tracking regulatory submissions and approvals ... IQVIA is a leading global provider of clinical research services, commercial insights and health ...
At AstraZeneca, teams work across global boundaries to make an impact and find answers to complex ... lifecycle management strategy, including real-world- evidence (RWE) and effectiveness studies ...
At AstraZeneca, teams work across global boundaries to make an impact and find answers to complex ... lifecycle management strategy, including real-world- evidence (RWE) and effectiveness studies ...
At AstraZeneca, teams work across global boundaries to make an impact and find answers to complex ... lifecycle management strategy, including real-world- evidence (RWE) and effectiveness studies ...
At AstraZeneca, teams work across global boundaries to make an impact and find answers to complex ... lifecycle management strategy, including real-world- evidence (RWE) and effectiveness studies ...
Newark, DE · On-site
$81K - $110K/yr
Compiles case studies and analyses of industrial accident causes and hazards to health for use as ... Participates as an active member of the Global EH&S Leadership Team (EHS LT) * Supports other ...
Newark, DE · On-site
$81K - $110K/yr
Compiles case studies and analyses of industrial accident causes and hazards to health for use as ... Participates as an active member of the Global EH&S Leadership Team (EHS LT) * Supports other ...
$81K - $110K/yr
Compiles case studies and analyses of industrial accident causes and hazards to health for use as ... Participates as an active member of the Global EH&S Leadership Team (EHS LT) * Supports other ...
$81K - $110K/yr
Compiles case studies and analyses of industrial accident causes and hazards to health for use as ... Participates as an active member of the Global EH&S Leadership Team (EHS LT) * Supports other ...
Wilmington, DE · On-site
... study designs and/or analyses. * Present data and recommendations to global program teams, external collaborators and senior management. * Build, verify, qualify, and apply PBPK models using ...
Wilmington, DE · On-site
... study designs and/or analyses. * Present data and recommendations to global program teams, external collaborators and senior management. * Build, verify, qualify, and apply PBPK models using ...
Wilmington, DE · On-site
... study designs and/or analyses. * Present data and recommendations to global program teams, external collaborators and senior management. * Build, verify, qualify, and apply PBPK models using ...
Wilmington, DE · On-site
... study designs and/or analyses. * Present data and recommendations to global program teams, external collaborators and senior management. * Build, verify, qualify, and apply PBPK models using ...
Wilmington, DE · On-site
$77K - $105K/yr
... clinical study reports (CSRs), investigator materials, regulatory documents, publications, and ... of global clinical trials. * Identifies, evaluates, and proactively manages clinical and program ...
Wilmington, DE · On-site
$77K - $105K/yr
... clinical study reports (CSRs), investigator materials, regulatory documents, publications, and ... of global clinical trials. * Identifies, evaluates, and proactively manages clinical and program ...
Wilmington, DE · On-site
Work closely with the project manager, scientists, and research associates in a collaborative, team ... Perform microbiology tests and studies within Energy and Water applications, including but not ...
Wilmington, DE · On-site
Work closely with the project manager, scientists, and research associates in a collaborative, team ... Perform microbiology tests and studies within Energy and Water applications, including but not ...
... weight management). Experience/knowledge in immunology and/or cell therapy also preferred ... studies), and/or substantial RWE experience Desirable Skills/Experience * Global and/or R&D ...
... weight management). Experience/knowledge in immunology and/or cell therapy also preferred ... studies), and/or substantial RWE experience Desirable Skills/Experience * Global and/or R&D ...
... weight management). Experience/knowledge in immunology and/or cell therapy also preferred ... studies), and/or substantial RWE experience Desirable Skills/Experience * Global and/or R&D ...
... weight management). Experience/knowledge in immunology and/or cell therapy also preferred ... studies), and/or substantial RWE experience Desirable Skills/Experience * Global and/or R&D ...
... weight management). Experience/knowledge in immunology and/or cell therapy also preferred ... studies), and/or substantial RWE experience Desirable Skills/Experience * Global and/or R&D ...
... weight management). Experience/knowledge in immunology and/or cell therapy also preferred ... studies), and/or substantial RWE experience Desirable Skills/Experience * Global and/or R&D ...
... weight management). Experience/knowledge in immunology and/or cell therapy also preferred ... studies), and/or substantial RWE experience Desirable Skills/Experience * Global and/or R&D ...
... weight management). Experience/knowledge in immunology and/or cell therapy also preferred ... studies), and/or substantial RWE experience Desirable Skills/Experience * Global and/or R&D ...
Overview Incyte is a global, science-driven biopharmaceutical company recognized for its strong ... Clinical lead for study abstracts, posters, oral presentations, and manuscripts for assigned ...
Overview Incyte is a global, science-driven biopharmaceutical company recognized for its strong ... Clinical lead for study abstracts, posters, oral presentations, and manuscripts for assigned ...
Overview Incyte is a global, science-driven biopharmaceutical company recognized for its strong ... Clinical lead for study abstracts, posters, oral presentations, and manuscripts for assigned ...
Overview Incyte is a global, science-driven biopharmaceutical company recognized for its strong ... Clinical lead for study abstracts, posters, oral presentations, and manuscripts for assigned ...
This role evaluates clinical quality systems, supports global regulatory compliance and provides ... Manage key components of the compliance audit program under the Community of Practice for Quality ...
This role evaluates clinical quality systems, supports global regulatory compliance and provides ... Manage key components of the compliance audit program under the Community of Practice for Quality ...
This role evaluates clinical quality systems, supports global regulatory compliance and provides ... Manage key components of the compliance audit program under the Community of Practice for Quality ...
This role evaluates clinical quality systems, supports global regulatory compliance and provides ... Manage key components of the compliance audit program under the Community of Practice for Quality ...
We provide our global teams with the resources needed to achieve individual career goals while ... What you will do: • Manage proposal bid and budget negotiation process, synthesizing detailed ...
We provide our global teams with the resources needed to achieve individual career goals while ... What you will do: • Manage proposal bid and budget negotiation process, synthesizing detailed ...
Wilmington, DE · On-site
Fish & Richardson, an AmLaw 65 global IP firm, is seeking a Litigation Paralegal to provide high ... Own end-to-end case management, including repository creation, document organization, and oversight ...
Wilmington, DE · On-site
Fish & Richardson, an AmLaw 65 global IP firm, is seeking a Litigation Paralegal to provide high ... Own end-to-end case management, including repository creation, document organization, and oversight ...
Wilmington, DE · On-site
Fish & Richardson, an AmLaw 65 global IP firm, is seeking a Litigation Paralegal to provide high ... Own end-to-end case management, including repository creation, document organization, and oversight ...
Wilmington, DE · On-site
Fish & Richardson, an AmLaw 65 global IP firm, is seeking a Litigation Paralegal to provide high ... Own end-to-end case management, including repository creation, document organization, and oversight ...
$23K - $30.3K
4% of jobs
$30.3K - $37.5K
10% of jobs
$43.3K is the 25th percentile. Wages below this are outliers.
$37.5K - $44.7K
14% of jobs
$44.7K - $52K
16% of jobs
The median wage is $58.2K / yr.
$52K - $59.2K
7% of jobs
$59.2K - $66.4K
10% of jobs
$70K is the 75th percentile. Wages above this are outliers.
$66.4K - $73.7K
29% of jobs
$73.7K - $80.9K
4% of jobs
$80.9K - $88.1K
3% of jobs
$88.1K - $95.4K
1% of jobs
$95.4K - $102.6K
2% of jobs
$23K
$61.4K
$102.6K
8.1
Based on 53 frontline employees who took The Breakroom Quiz
61st of 223 rated it services
IQVIA is seeking a CRA 2 with a minimum of 1.5 years of on-site oncology monitoring experience:
Essential Functions
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
Education: Bachelor's Degree (Degree in scientific discipline or health care preferred)
Experience: 1.5 to 2 years of relevant CRA experience including on-site monitoring.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $87,200.00 - $145,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
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At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.
Health care and social assistance
10,000+ Employees
Durham, NC, US
