... operations and clinical research activities. * Identify, plan, and develop administrative policies for assigned departments, and assist in reviewing and implementing institutional and departmental ...
Quick apply
... operations and clinical research activities. * Identify, plan, and develop administrative policies for assigned departments, and assist in reviewing and implementing institutional and departmental ...
Quick apply
... operations and clinical research activities. * Identify, plan, and develop administrative policies for assigned departments, and assist in reviewing and implementing institutional and departmental ...
Stamford, CT · On-site
About BestEx Research BestEx Research is an award-winning, high-growth, profitable algorithmic ... operational backbone of his day. The ideal partner in the role is a driven individual who can ...
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Stamford, CT · On-site
About BestEx Research BestEx Research is an award-winning, high-growth, profitable algorithmic ... operational backbone of his day. The ideal partner in the role is a driven individual who can ...
Fairfield, CT · On-site
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
Fairfield, CT · On-site
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
Stamford, CT · On-site
About BestEx Research BestEx Research is an award-winning, high-growth, profitable algorithmic ... operational backbone of his day. The ideal partner in the role is a driven individual who can ...
Stamford, CT · On-site
About BestEx Research BestEx Research is an award-winning, high-growth, profitable algorithmic ... operational backbone of his day. The ideal partner in the role is a driven individual who can ...
... from Clinical Research Operations Accountable and responsible for assigned synopsis and study ... sign-off Assist with internal and external dissemination of results to Development Team ...
... from Clinical Research Operations Accountable and responsible for assigned synopsis and study ... sign-off Assist with internal and external dissemination of results to Development Team ...
New Haven, CT · On-site
... regulatory requirements. * Assist with study feasibility reviews by evaluating protocol ... and operational considerations. * Adhere strictly to study protocols, maintain accurate and ...
New Haven, CT · On-site
... regulatory requirements. * Assist with study feasibility reviews by evaluating protocol ... and operational considerations. * Adhere strictly to study protocols, maintain accurate and ...
New Haven, CT · On-site
... regulatory requirements. * Assist with study feasibility reviews by evaluating protocol ... and operational considerations. * Adhere strictly to study protocols, maintain accurate and ...
Quick apply
New Haven, CT · On-site
... regulatory requirements. * Assist with study feasibility reviews by evaluating protocol ... and operational considerations. * Adhere strictly to study protocols, maintain accurate and ...
... regulatory requirements. * Assist with study feasibility reviews by evaluating protocol ... and operational considerations. * Adhere strictly to study protocols, maintain accurate and ...
Quick apply
... regulatory requirements. * Assist with study feasibility reviews by evaluating protocol ... and operational considerations. * Adhere strictly to study protocols, maintain accurate and ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
... operation of clinical trials as per GCP and ICH guidelines including participant recruitment ... • Assist regulatory staff with study regulatory reporting requirements and IRB policies for ...
$10.52 - $12.22
0% of jobs
$12.22 - $13.93
12% of jobs
$15.07 is the 25th percentile. Wages below this are outliers.
$13.93 - $15.63
20% of jobs
$15.63 - $17.34
16% of jobs
The median wage is $17.57 / hr.
$17.34 - $19.04
19% of jobs
$20.60 is the 75th percentile. Wages above this are outliers.
$19.04 - $20.75
9% of jobs
$20.75 - $22.45
11% of jobs
$22.45 - $24.16
6% of jobs
$24.16 - $25.86
3% of jobs
$25.86 - $27.57
2% of jobs
$27.57 - $29.27
2% of jobs
$10
$18
$29
| Aspect | Research Operations Assistant | Research Coordinator |
|---|---|---|
| Credentials | Typically requires a bachelor's degree in a related field; certifications are a plus | Usually holds a bachelor's or master's degree; certifications in research management are common |
| Work Environment | Supports research teams in labs or office settings, handling administrative and logistical tasks | Manages research projects, coordinates activities, and liaises with stakeholders |
| Employer & Industry Usage | Found in academic, healthcare, and corporate research settings | Common in clinical, academic, and industry research projects |
The Research Operations Assistant primarily provides administrative and logistical support within research teams, focusing on day-to-day operations. In contrast, the Research Coordinator manages research projects, oversees compliance, and coordinates between teams and stakeholders. Both roles require similar educational backgrounds but differ in scope and responsibilities.
Full-time
Posted 10 days ago
This Lab Manager role provides strategic and operational leadership for multiple clinical research laboratories across several locations in Connecticut. The position focuses on overseeing both wet and dry lab operations, managing laboratory resources and kit inventory, and ensuring laboratories can effectively support complex clinical trials, particularly in oncology. The Lab Manager leads a team of laboratory supervisors, shapes broader operational strategy, and partners closely with clinical research leadership to maintain high standards of quality, safety, and regulatory compliance in an academic medical center and cancer research environment.
ResponsibilitiesThe role is based within an academic medical center and cancer research setting, providing the opportunity to contribute to a nationally recognized research institution with a strong focus on oncology and clinical trials. The Lab Manager oversees laboratory supervisors and operations across multiple locations in Connecticut, including sites such as Greenwich, North Haven, New Haven, and Trumbull, and will travel between these locations as needed. The environment includes both wet and dry laboratories operating at BSL-2 standards, with a strong emphasis on complex specimen processing, clinical trial support, and adherence to regulatory and institutional policies. The culture is highly mission-driven, with a focus on advancing clinical research, supporting patient care, and fostering collaboration among clinical, research, and administrative teams. Staff use standard office technologies and software, including Microsoft Office and clinical or laboratory information systems such as EPIC or similar platforms. The position involves a mix of on-site laboratory oversight, administrative and strategic planning responsibilities, and cross-functional collaboration within a structured yet purpose-driven academic and research setting.
Job Type & LocationThis is a Permanent position based out of New Haven, CT.
Pay and BenefitsThe pay range for this position is $82000.00 - $131500.00/yr.
Will take Yale's benefits if DP, Actalent benefits if C2H.
Workplace TypeThis is a fully onsite position in New Haven,CT.
Application DeadlineThis position is anticipated to close on Aug 14, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.
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Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
5,001 - 10,000 Employees
Hanover, MD, US
1983