A Bachelor's degree and/or relevant certifications (CRM, CRA, CIPP, CGRP, FOIA Professional ... Full-time and part-time employees working at least 20 hours a week on a regular basis are eligible ...
Quick apply
A Bachelor's degree and/or relevant certifications (CRM, CRA, CIPP, CGRP, FOIA Professional ... Full-time and part-time employees working at least 20 hours a week on a regular basis are eligible ...
Quick apply
A Bachelor's degree and/or relevant certifications (CRM, CRA, CIPP, CGRP, FOIA Professional ... Full-time and part-time employees working at least 20 hours a week on a regular basis are eligible ...
$13.61 - $19.55
0% of jobs
$19.55 - $25.49
8% of jobs
$25.49 - $31.43
13% of jobs
$33.02 is the 25th percentile. Wages below this are outliers.
$31.43 - $37.37
15% of jobs
$37.37 - $43.31
13% of jobs
The median wage is $44.21 / hr.
$43.31 - $49.25
11% of jobs
$49.25 - $55.19
12% of jobs
$57.30 is the 75th percentile. Wages above this are outliers.
$55.19 - $61.13
13% of jobs
$61.13 - $67.07
14% of jobs
$67.07 - $73.02
2% of jobs
$73.02 - $78.96
1% of jobs
$13
$46
$78
To thrive as a Part Time CRA (Clinical Research Associate), you need a background in life sciences or a related field, an understanding of clinical trial processes, and prior experience in clinical research. Familiarity with electronic data capture systems, Good Clinical Practice (GCP) certification, and knowledge of regulatory guidelines are often required. Excellent organizational, communication, and problem-solving skills help with managing multiple study sites and working independently. These competencies are crucial for ensuring clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards.
A typical work week for a Part Time CRA may include monitoring study sites remotely or in person, reviewing trial documentation, ensuring regulatory compliance, and communicating updates to site staff and sponsors. You may also be responsible for verifying data accuracy, assisting with site training, and resolving any study-related issues that arise. The workload can vary depending on the stage of the clinical trial and the number of assigned sites, but flexibility and effective time management are essential. Team collaboration is common, as you'll coordinate closely with investigators, research coordinators, and project managers to ensure smooth trial operations.
A Part-Time Clinical Research Associate (CRA) is responsible for monitoring clinical trials to ensure compliance with regulatory guidelines, protocols, and good clinical practices. They typically work on a reduced schedule while overseeing site activities, ensuring data accuracy, and maintaining communication with investigators. Part-time CRAs may be employed by pharmaceutical companies, contract research organizations (CROs), or healthcare institutions. This role is ideal for professionals seeking flexibility while contributing to the success of clinical research.
Full-time, Part-time
Medical, Retirement, PTO
Posted 24 days ago
Are you looking for a Challenge? Looking for an innovative organization and the opportunity to learn and grow professionally? We can help! We are seeking a Records Management Specialist to provide on-demand Cybersecurity and IT services to support the National Indian Gaming Commission (NIGC) mission at the NIGC Headquarters in Washington, D.C.
I've never heard of Terrestris. What do you do?
At Terrestris, we leverage technology to create better mission outcomes through better human performance. We form strong client and team relationships through transparency and strive to create an environment where our team can let their excellence shine through.By finding, developing, and incorporating new ideas, we provide memorable services. Rooted in the USMC values of honor, courage, and commitment, Terrestris seeks to deliver extraordinary value to the American people by helping the Government become more efficient and effective.
So, what will the Records Management Specialist at Terrestris do?
The Records Management Specialist organizes, maintains, and safeguards official agency records to ensure they are accurate, accessible, and compliant with federal records laws and policies. In support of the National Indian Gaming Commission (NIGC), this role helps manage digital and physical records related to cybersecurity, IT operations, and agency programs, ensuring proper retention, security, and retrieval of critical information. They also support audits, records disposition, and information governance to help the agency operate efficiently and securely.
What does a typical day look like for a Records Management Specialist?
You will:
What qualifications do you look for?
You might be the professional we're looking for if you have:
What kind of benefits does Terrestris Offer?
We offer outstanding benefits including health, financial, and retirement benefits, as well as paid leave, professional development, tuition assistance, and work-life programs. Our award programs acknowledge employees for exceptional performance and superior demonstration of our service standards. Full-time and part-time employees working at least 20 hours a week on a regular basis are eligible to participate in our benefit programs. Other offerings may be provided for employees not within this category.
Terrestris is an Equal Opportunity Employer (EOE). Qualified applicants are considered for employment without regard to age, race color, religion, sex, national origin, sexual orientation, disability, or veteran status. Applicants must be authorized to work in the U.S.
DILBERT 2018 Scott Adams. Used By permission of ANDREWS MCMEEL SYNDICATION. All rights reserved.