Wilmington, DE Contract Duration: 12-36 months Rate: Negotiable Responsibilities: * Excellent ... Support the CRA in the maintenance and close out activities for the ISF. * Contribute to the ...
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Wilmington, DE Contract Duration: 12-36 months Rate: Negotiable Responsibilities: * Excellent ... Support the CRA in the maintenance and close out activities for the ISF. * Contribute to the ...
Post Award Specialist
Wilmington, DE · On-site
... contract provisions Qualifications: * Bachelor Degree required; Accounting or Finance Degree is ... CRA, CPRA, and/or CFRA preferred About Us Nemours Children's Health is an internationally ...
Post Award Specialist
Wilmington, DE · On-site
... contract provisions Qualifications: * Bachelor Degree required; Accounting or Finance Degree is ... CRA, CPRA, and/or CFRA preferred About Us Nemours Children's Health is an internationally ...
Post Award Specialist
Wilmington, DE · On-site
... contract provisions Qualifications: * Bachelor Degree required; Accounting or Finance Degree is ... CRA, CPRA, and/or CFRA preferred Nemours Children's Health is an internationally recognized ...
Post Award Specialist
Wilmington, DE · On-site
... contract provisions Qualifications: * Bachelor Degree required; Accounting or Finance Degree is ... CRA, CPRA, and/or CFRA preferred Nemours Children's Health is an internationally recognized ...
Contract Cra information
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$12.03 - $17.28
0% of jobs
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8% of jobs
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$29.18 is the 25th percentile. Wages below this are outliers.
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The median wage is $39.06 / hr.
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$50.63 is the 75th percentile. Wages above this are outliers.
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2% of jobs
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1% of jobs
$12
$41
$69
How much do contract cra jobs pay per hour?
As of Jul 28, 2026, the average hourly pay for contract cra in Delaware is $41.16, according to ZipRecruiter salary data. Most workers in this role earn between $28.89 and $52.69 per hour, depending on experience, location, and employer.
What are some common challenges faced by Contract Clinical Research Associates (CRAs) and how can they effectively manage them?
Contract CRAs often juggle multiple clinical trial sites and studies, which can make prioritizing and time management especially challenging. They must adapt quickly to each sponsor's protocols and systems, often with limited onboarding. Building strong relationships with site staff and maintaining clear, consistent communication are key to overcoming these challenges. Staying organized through meticulous documentation and leveraging digital tools can help contract CRAs efficiently meet monitoring visit deadlines and regulatory requirements.
What are the key skills and qualifications needed to thrive as a Contract CRA (Clinical Research Associate), and why are they important?
To thrive as a Contract CRA, you need a solid understanding of clinical research protocols, regulatory guidelines (like GCP/ICH), and typically a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certifications like ACRP or SOCRA are beneficial. Strong attention to detail, excellent organizational skills, and effective communication are crucial soft skills for managing multiple studies and collaborating with sites. These competencies are essential for ensuring compliance, data integrity, and the smooth execution of clinical trials.
What Are Contract CRA Jobs?
A contract clinical research associate (contract CRA) is a temporary position in which you manage clinical trials and scientific research projects. As a contractor, you work temporarily on a contract that typically lasts for the duration of the project. Clinical research associates work in the pharmaceutical industry to ensure the safety and effectiveness of medication or vaccines. You can also work on studies for biotech companies and projects that perform analysis on surgical procedures or treatments. Your duties focus on planning the trial, defining the parameters, ensuring the safety of participants, and making sure the project meets all regulations and requirements.
What are contract crafters?
Contract crafters are professionals who specialize in creating, reviewing, and negotiating contracts for individuals or organizations. They ensure that agreements are legally sound, clearly written, and protect the interests of all parties involved. Contract crafters may work in a variety of industries, including business, law, real estate, and technology. Their expertise helps minimize risk and ensure compliance with relevant laws and regulations.
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Contractor
Posted 17 days ago
Job description
Wilmington, DE
Contract Duration: 12-36 months
Rate: Negotiable
Responsibilities:
- Excellent employment opportunity for a Specialist Study Management in the Wilmington, DE area. Candidates must be local to Wilmington, DE, non-remote position
- Own and maintain quality for the study file as the local study team TMF owner
- Responsible for site communications and other portal management
- Running and analyzing reports from multiple systems
- Responsible for Vendor Management
- Handle requests for CTMS updates
- Operational responsibility to set-up the local Trial Master File (eTMF) including tracking of documents.
- Maintain and close the local TMF ensuring International Conference of Harmonisation Guidelines for Good Clinical Practice (ICH/GCP) compliance and local requirements.
- Support the CRA in the maintenance and close out activities for the ISF.
- Contribute to the production and maintenance of study documents, ensuring template and version compliance.
- Contribute to electronic applications/submissions by handling clinical-regulatory documents according to the requested technical standards i.e., Submission Ready Standards (SRS), supporting effective publishing and delivery to regulatory authorities (not for international studies).
Experience:
- Bachelor's Degree is preferred
- 3-5 years of experience in Clinical Trials and Regulatory documents is required
- Veeva experience a plus
- Must be methodical, compliant to processes yet flexible when needed
- High ability to manage priorities and Local Study Team expectations
- Independent yet able to work cohesively with a team
- Experience with electronic trial master file system(s) including uploading, reviewing, QC, approval of study required documents.
- Working knowledge of the Clinical Study Process and an understanding of the range of working procedures relating to it, together with an understanding of the ICH/GCP guidelines
- Working knowledge of clinical study documents
- Ability to develop advanced computer skills to increase efficiency in day-to-day tasks
- Good verbal and written communication
- Good interpersonal skills and ability to work in an international team environment
- Willingness and ability to train others on study administration procedures
- Display excellent organization and time management skills