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Study Manager Jobs in Connecticut (NOW HIRING)

IQVIA

Mgr, Database Management Systems

Hartford, CT · On-site

Mgr, Database Management Systems Designs or modifies data models to solve complex database ... Share new industry standards and best practices with project and study teams and departments as ...

IQVIA

Mgr, Database Management Systems

Hartford, CT · On-site

Mgr, Database Management Systems Designs or modifies data models to solve complex database ... Share new industry standards and best practices with project and study teams and departments as ...

Integrated Resources INC

Quality Lead

Groton, CT

... study teams. Interaction with: A diverse range of stakeholders from varying internal lines Ability to: be an effective project manager, leadership of Significant Quality Event Teams and/or ...

Tighe & Bond

Traffic Project Manager 1

Shelton, CT · Hybrid

$108K - $142K/yr

Serving as project manager for traffic impact studies, corridor studies, intersection improvements, traffic signal design, safety evaluations, and multimodal transportation projects * Developing ...

Tighe & Bond

Traffic Project Manager 1

Middletown, CT · On-site +1

$108K/yr

Serving as project manager for traffic impact studies, corridor studies, intersection improvements, traffic signal design, safety evaluations, and multimodal transportation projects * Developing ...

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Study Manager information

See Connecticut salary details

$23.3K

$56.6K

$110.3K

How much do study manager jobs pay per year?

As of Aug 6, 2026, the average yearly pay for study manager in Connecticut is $56,625.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,000.00 and $65,200.00 per year, depending on experience, location, and employer.

How does a study manager typically collaborate with cross-functional teams during the course of a clinical trial?

As a Study Manager, you'll work closely with cross-functional teams including clinical research associates, data managers, regulatory affairs, and biostatisticians to ensure the trial progresses smoothly and meets regulatory requirements. Regular meetings, status updates, and shared project management tools facilitate clear communication and timely issue resolution. You will often serve as the central point of contact, coordinating tasks and resolving conflicts between departments to keep the study on track. Collaboration skills are essential, as you’ll need to balance input from multiple stakeholders while maintaining study timelines and quality standards.

What are the key skills and qualifications needed to thrive as a study manager?

To thrive as a Study Manager, you need a solid background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification is typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating teams and stakeholders. These qualifications ensure the successful planning, execution, and oversight of clinical studies within regulatory and timeline requirements.

What does a study manager do?

A Study Manager is responsible for overseeing the planning, execution, and completion of research studies, often in clinical or academic settings. They coordinate between various stakeholders, including research teams, sponsors, and regulatory authorities, to ensure studies are conducted efficiently and in compliance with relevant guidelines. Study Managers manage timelines, budgets, and resources, while also handling documentation and reporting requirements. Their role is critical to ensuring that studies meet their scientific objectives and adhere to ethical standards.
What are the most commonly searched types of Study jobs in Connecticut? The most popular types of Study jobs in Connecticut are:
Study Manager jobs near you
Infographic showing various Study Manager job openings in Connecticut as of August 2026, with employment types broken down into 84% Full Time, 11% Part Time, 3% Temporary, and 2% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $56,625 per year, or $27.2 per hour.

In Vitro Pharmacologist

Integrated Resources INC

Groton, CT

Contractor

Re-posted 2 days ago

Job description

Company Description

A Few Words About Us - 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.


This position is with my direct client 

Job Description

Our Client is looking for "In-Vitro Pharmacologist" with knowledge of "High Throughput Screening" and "Assay Development"

Job Summary-

The Primary Pharmacology Group is actively supporting Cystic Fibrosis projects in developing assays, running subset screens, and external data management.


Job responsibilities include performing routine tasks associated directly with the Cystic Fibrosis projects or indirectly in a capacity easing role to support these projects.


The successful candidate will join a team of scientists focused on assay development and execution of primary and secondary plate-based assays for multiple therapeutic areas.

Qualifications

Qualification-

Applicants must have demonstrated experience with de-novo assay development, optimization, and in vitro screening experience across a range of biochemical and cell-based functional formats as well as cell culture expertise.


Experience with high-throughput screening techniques is advantageous and comfort with relevant software tools such as ABase, Spotfire and GraphPad Prism is preferred.


The successful candidate will be excited by a role with high demands and should possess strong collaborative and communication skills.


He/she should be adept at multi-tasking, integrating biology concepts from group discussions and the literature, and comfortable working in a team environment.


4-7 years of experience in Assays studies


Experience in High Throughput Screening and plate based assay

Additional Information

Regards

Pooja Mishra

Clinical Recruiter

Integrated Resources, Inc. 

IT Life Sciences Allied Healthcare CRO

Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I

Tel: 732 429 1636

(W) 732-549-2030 x 214 | (F) 732-549-5549

Gold Seal JCAHO Certified for Health Care Staffing 

"INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row)



Integrated Resources logo

About Integrated Resources

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.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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