Assumes project management responsibilities for selected studies and site management activities as ... May be responsible for clinical supply operations, site and vendor selection. * People working ...
Assumes project management responsibilities for selected studies and site management activities as ... May be responsible for clinical supply operations, site and vendor selection. * People working ...
Sr Clinical Research Spec
North Haven, CT · On-site
Assumes project management responsibilities for selected studies and site management activities as ... May be responsible for clinical supply operations, site and vendor selection. * People working ...
Sr Clinical Research Spec
North Haven, CT · On-site
Assumes project management responsibilities for selected studies and site management activities as ... May be responsible for clinical supply operations, site and vendor selection. * People working ...
Senior Clinical Manager
Westport, CT · On-site +1
$90K - $100K/yr
Senior Clinical Manager Experience Camps is a national nonprofit that transforms the lives of grieving children through no-cost summer camps, year-round programs, and a culture-shifting movement to ...
Senior Clinical Manager
Westport, CT · On-site +1
$90K - $100K/yr
Senior Clinical Manager Experience Camps is a national nonprofit that transforms the lives of grieving children through no-cost summer camps, year-round programs, and a culture-shifting movement to ...
Clinical Lab Assistant
Stamford, CT · On-site
Stand for 2-4 hours at a time for execution of clinical studies * Assist Clinical Coordinators in preparing and executing clinical studies * Prepare documents for clinical studies, assist in study ...
Clinical Lab Assistant
Stamford, CT · On-site
Stand for 2-4 hours at a time for execution of clinical studies * Assist Clinical Coordinators in preparing and executing clinical studies * Prepare documents for clinical studies, assist in study ...
Responsible for study/project management within the unit including study scheduling, protocol planning(start up activity) and is the the primary contact for the project teams responsible for the ...
Responsible for study/project management within the unit including study scheduling, protocol planning(start up activity) and is the the primary contact for the project teams responsible for the ...
Clinical Program Manager
New Haven, CT · On-site
Responsible for study/project management within the unit including study scheduling, protocol planning(start up activity) and is the the primary contact for the project teams responsible for the ...
Clinical Program Manager
New Haven, CT · On-site
Responsible for study/project management within the unit including study scheduling, protocol planning(start up activity) and is the the primary contact for the project teams responsible for the ...
Clinical Program Manager
New Haven, CT · On-site
Leads the cross-functional execution of one or more clinical studies conducted within the Clinical ... management of cross-study activities and coordination of CRU functional line data review ...
Clinical Program Manager
New Haven, CT · On-site
Leads the cross-functional execution of one or more clinical studies conducted within the Clinical ... management of cross-study activities and coordination of CRU functional line data review ...
Clinical Lab Assistant
Stamford, CT · On-site
$25 - $32/hr
GENERAL Assist Clinical Coordinators in preparing and executing clinical studies which support ... Consulting, Professional Engineering, Industrial Maintenance and Facility Management, Contracted ...
Clinical Lab Assistant
Stamford, CT · On-site
$25 - $32/hr
GENERAL Assist Clinical Coordinators in preparing and executing clinical studies which support ... Consulting, Professional Engineering, Industrial Maintenance and Facility Management, Contracted ...
Clinical Scientist
Guilford, CT · On-site
$128K - $147K/yr
You will be responsible for contributing to clinical study design, supporting study execution, and ... Strong organizational skills and ability to manage multiple projects simultaneously * Ability to ...
Clinical Scientist
Guilford, CT · On-site
$128K - $147K/yr
You will be responsible for contributing to clinical study design, supporting study execution, and ... Strong organizational skills and ability to manage multiple projects simultaneously * Ability to ...
Clinical Scientist
$128K - $147K/yr
You will be responsible for contributing to clinical study design, supporting study execution, and ... Strong organizational skills and ability to manage multiple projects simultaneously * Ability to ...
Quick apply
Clinical Scientist
$128K - $147K/yr
You will be responsible for contributing to clinical study design, supporting study execution, and ... Strong organizational skills and ability to manage multiple projects simultaneously * Ability to ...
Clinical Scientist
$128K - $147K/yr
You will be responsible for contributing to clinical study design, supporting study execution, and ... Strong organizational skills and ability to manage multiple projects simultaneously * Ability to ...
Clinical Scientist
$128K - $147K/yr
You will be responsible for contributing to clinical study design, supporting study execution, and ... Strong organizational skills and ability to manage multiple projects simultaneously * Ability to ...
Provide product training and support to clinical sites for the pill cam procedure. Support the ... Managing and maintaining study documents and trial supplies, colonoscopy forceps, FedEx envelop ...
Provide product training and support to clinical sites for the pill cam procedure. Support the ... Managing and maintaining study documents and trial supplies, colonoscopy forceps, FedEx envelop ...
... Management. The ideal candidate combines strong programming skills with clinical study experience and can build practical solutions that improve how teams access, analyze, visualize, and work with ...
New
Quick apply
... Management. The ideal candidate combines strong programming skills with clinical study experience and can build practical solutions that improve how teams access, analyze, visualize, and work with ...
New
Managing and maintaining study documents and trial supplies, colonoscopy forceps, FedEx envelop, IWRS User information. * Administer, Maintain and coordinate the logistic aspects of clinical trials ...
Managing and maintaining study documents and trial supplies, colonoscopy forceps, FedEx envelop, IWRS User information. * Administer, Maintain and coordinate the logistic aspects of clinical trials ...
Medical Writer / Clinical Document Author
Stamford, CT · Remote
$50 - $80/hr
Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...
Medical Writer / Clinical Document Author
Stamford, CT · Remote
$50 - $80/hr
Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...
Medical Writer / Clinical Document Author
Waterbury, CT · Remote
$50 - $80/hr
Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...
Medical Writer / Clinical Document Author
Waterbury, CT · Remote
$50 - $80/hr
Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...
Medical Writer / Clinical Document Author
New Haven, CT · Remote
$50 - $80/hr
Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...
Medical Writer / Clinical Document Author
New Haven, CT · Remote
$50 - $80/hr
Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...
Medical Writer / Clinical Document Author
Hartford, CT · Remote
$50 - $80/hr
Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...
Medical Writer / Clinical Document Author
Hartford, CT · Remote
$50 - $80/hr
Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...
Medical Writer / Clinical Document Author
Bridgeport, CT · Remote
$50 - $80/hr
Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...
Medical Writer / Clinical Document Author
Bridgeport, CT · Remote
$50 - $80/hr
Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...
Clinical Development Scientist
$203K - $305K/yr
... questions; manage and resolve issues that could impede study conduct. * Clinical Development ... Planning: Support the design and execution of key elements of the Clinical Development Plan ...
Clinical Development Scientist
$203K - $305K/yr
... questions; manage and resolve issues that could impede study conduct. * Clinical Development ... Planning: Support the design and execution of key elements of the Clinical Development Plan ...
Clinical Study Manager information
See Connecticut salary details
$27.44 - $33.26
4% of jobs
$33.26 - $39.08
6% of jobs
$39.08 - $44.90
7% of jobs
$49.27 is the 25th percentile. Wages below this are outliers.
$44.90 - $50.72
9% of jobs
$50.72 - $56.55
15% of jobs
The median wage is $59.11 / hr.
$56.55 - $62.37
18% of jobs
$66.51 is the 75th percentile. Wages above this are outliers.
$62.37 - $68.19
21% of jobs
$68.19 - $74.01
7% of jobs
$74.01 - $79.83
6% of jobs
$79.83 - $85.65
3% of jobs
$85.65 - $91.47
2% of jobs
$27
$59
$91
How much do clinical study manager jobs pay per hour?
What are the key skills and qualifications needed to thrive as a clinical study manager?
What are some common challenges faced by clinical study managers, and how can they be addressed?
How much does a clinical study manager earn?
What does a clinical study manager do?
What are the most commonly searched types of Clinical Study jobs in Connecticut?
The most popular types of Clinical Study jobs in Connecticut are:
What are popular job titles related to Clinical Study Manager jobs in Connecticut?
For Clinical Study Manager jobs in Connecticut, the most frequently searched job titles are:
What job categories do people searching Clinical Study Manager jobs in Connecticut look for?
The top searched job categories for Clinical Study Manager jobs in Connecticut are:
- Remote Clinical Research Oncology
- Sr Clinical Research Coordinator
- Flex Time Remote Clinical Research
- Clinical Research Organization
- Parasitology Remote
- Clinical Research Project Manager
- Contract Clinical Research
- Senior Clinical Research Associate
- Senior Ucsf Clinical Research
- Clinical Research Coordinator 2
What cities in Connecticut are hiring for Clinical Study Manager jobs?
Cities in Connecticut with the most Clinical Study Manager job openings:

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 11 days ago
Medtronic rating
7.8
Based on 178 frontline employees who took The Breakroom Quiz
175th of 543 rated manufacturers
Job description
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first - developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
A Day in the LifeIn this exciting role as a Senior Clinical Research Specialist (Sr. CRS) in our Surgical Operating Unit, you will have primary responsibility in the execution and oversight of global clinical studies. An individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower-level professionals. Most of the time is spent delivering and overseeing the projects - from design to implementation - while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education. Assumes project management responsibilities for selected studies and site management activities as needed.Responsibilities may include the following and other duties may be assigned.
- Oversees, designs, plans and develops clinical evaluation research studies.
- Prepares and authors protocols and patient record forms.
- Conducts registered and non-registered clinical studies of products that have been determined to satisfy a medical need and/or offer a commercial potential.
- Oversees and interpret results of clinical investigations in preparation for new drug device or consumer application.
- Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations, and may prepare clinical trial budgets.
- May be responsible for clinical supply operations, site and vendor selection.
- People working within region/country may also have the responsibilities that include:
- Represents Medtronic from a clinical research respective within the country / region and also collects feedback from local customers and authorities.
- Builds and maintains optimal relationships and effective collaborations with various internal and external parties.
- Drives local evidence dissemination & awareness.
Must Have:MinimumRequirements
- Bachelor's degreerequired
- Minimum of4years of relevant experience, or advanced degree with a minimum of2years of relevant experience.
Nice to Have
- Knowledge of Medtronicsystems
- Understanding of the clinical Quality and Regulatoryenvironments
- Experience in the Medical Device Industry.
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
U.S. Work Authorization & Sponsorship
At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Recruitment Fraud Alert
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.
Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.
If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.
If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.
Benefits & CompensationMedtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance,Health Savings Account,Healthcare Flexible Spending Account,Life insurance, Long-term disability leave,Dependent daycare spending account,Tuition assistance/reimbursement, andSimple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees:Incentive plans, 401(k) plan plus employer contribution and match,Short-term disability,Paid time off,Paid holidays,Employee Stock Purchase Plan,Employee Assistance Program,Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), andCapital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can findhere a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
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