Top 322 Clinical study manager Jobs in Remote U.s.

Assistant Clinical Study Manager
RTI International —Remote
- $78,000 - $95,000 a year
- Full-time
- Microsoft Outlook
- Mid-level
- Master's degree
- Paid parental leave
- Disability insurance
1d
Clinical Study Project Manager
IUVO BIOSCIENCE OPERATIONS, LLC —Remote
- $110,000 - $140,000 a year
- Remote
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
Quick Apply
Clinical Study Manager
IUVO BIOSCIENCE OPERATIONS, LLC —Remote
- $100,000 - $150,000 a year
- Remote
- Microsoft Outlook
- Computer literacy
- Basic math
Quick Apply
Clinical Study Data Reviewer
IUVO BIOSCIENCE OPERATIONS, LLC —Remote
- $60,000 - $74,000 a year
- Remote
- Computer literacy
- Writing skills
- HIPAA
Quick Apply
Regional Clinical Study Manager
BeiGene —Remote
- $118,600 - $158,600 a year
- Full-time
- Computer literacy
- Writing skills
- Data analysis skills
- Health savings account
- Employee stock purchase plan
Clinical Trial Manager
Generate Biomedicines —Somerville, MA
- $127,000 - $178,000 a year
- Remote
- Mid-level
- Bachelor's degree
- Travel
5d
Regional Clinical Study Senior Manager
BeiGene —Remote
- $136,400 - $181,400 a year
- Full-time
- 6 years
- Computer literacy
- Data analysis skills
- Health savings account
- Employee stock purchase plan
Senior CTMA Manager, Regional Clinical Study Management
BeiGene —Remote
- $136,400 - $181,400 a year
- Full-time
- Data analysis skills
- Microsoft Office
- Travel
- Health savings account
- Employee stock purchase plan
Central Study Coordinator I
Care Access —Boston, MA
- $75,000 - $95,000 a year
- Remote
- Spanish
- Microsoft Excel
- Microsoft Outlook
- Health savings account
- Paid holidays
7d
Clinical Project Manager (US)
Alimentiv —Raleigh-Durham, NC
- $95,500 - $159,000 a year
- Full-time
- Remote
- English
- Mid-level
- Bachelor's degree
Quick Apply
Clinical Research Manager
Johns Hopkins University —Baltimore, MD
- $55,800 - $97,600 a year
- Full-time
- Remote
- Background check
- Master's degree
- Analysis skills
Clinical Trial Manager (Retina)
4D Molecular Therapeutics —Emeryville, CA
- $150,000 - $170,000 a year
- Remote
- Microsoft Excel
- 6 years
- Microsoft Outlook
Sr Clinical Study Manager
Penumbra —Remote
- $153,000 - $193,000 a year
- Remote
- 7 years
- Office
- Bachelor's degree
- Paid parental leave
- AD&D insurance
2h
Clinical Sample Manager
SAB —Remote
- $130,000 - $150,000 a year
- Full-time
- Microsoft Excel
- Bachelor's degree
- Travel
Quick Apply
14d
Clinical Trial Manager, Clinical Operations
Bristol-Myers Squibb —Remote
- $134,505 - $162,988 a year
- Email
- Remote
- 5 years
- Bachelor of Science
- Bachelor's degree
- Paid holidays
- Disability insurance
Senior Clinical Research Manager
BeiGene —Remote
- $136,400 - $181,400 a year
- Full-time
- 7 years
- Microsoft Excel
- Microsoft Outlook
- Health savings account
- Employee stock purchase plan
Clinical Project Manager (CRO) - Remote
C&R Research US —Remote
- $130,000 - $155,000 a year
- Part-time
- Remote
- Nursing
- Microsoft Excel
- HIPAA
- Paid time off
- Flexible schedule
Quick Apply
6d
Manager, Clinical Operations
IQVIA —Durham, NC
- $86,500 - $216,000 a year
- Full-time
- Remote
- Microsoft Excel
- English
- Mid-level
- Work from home
Clinical Trial Associate (Associate, Rater Services)
Cogstate —Remote
- $65,000 - $75,000 a year
- Full-time
- Remote
- Computer literacy
- Mid-level
- Bachelor's degree
- Paid holidays
- Disability insurance
Quick Apply
Senior Manager / Manager, Clinical Quality
Priovant Therapeutics —Remote
- Bachelor's degree
- Senior level

I want to receive the latest job alert for clinical study manager in remote u.s.

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

clinical study manager jobs near remote u.s.

Assistant Clinical Study Manager

RTI International -
Remote

Apply Now

Job Details

Full-time
$78,000 - $95,000 a year
1 day ago

Benefits

Paid parental leave
Disability insurance
Dental insurance
Paid time off
Parental leave
Employee assistance program

Qualifications

Meeting minutes
Project reporting
Research project management
Correspondence management
Microsoft Outlook
Training material drafting
Mid-level
Risk mitigation strategy implementation
Project communication management
Master's degree
Meeting scheduling
Bachelor's degree
Data management
Team training
Quality control operations
Technical writing
Project execution
Progress management
1 year
Clinical research documentation
Cross-functional collaboration
Technical Proficiency
Project stakeholder communication
Operations planning

Full Job Description

Why RTI:

RTI International is an independent, scientific research institute dedicated to improving the human condition. Our vision is to address the world's most critical problems with technical and science-based solutions in pursuit of a better future. Clients rely on us to answer questions that demand an objective and multidisciplinary approach—one that integrates expertise across social, statistical, data, and laboratory sciences, engineering, and other technical disciplines to solve the world’s most challenging problems.

We believe in the promise of science and technical solutions, and we push ourselves every day to deliver on that promise for the good of people, communities, and businesses in the US and around the world. If you are looking for the opportunity to make a real difference, RTI is the place for you.

About the Hiring Group:

RTI International, an independent nonprofit research institute dedicated to improving human condition, is seeking an Assistant Clinical Study Manager to join our team. The ideal candidate will be highly motivated, results-oriented, and collaborative with experience working as an integral member of a Data Coordinating Center clinical trial operations team. This position will work with RTI employees, Project Teams and contractors to support clinical research projects and data coordinating centers. The ideal candidate will be highly motivated, results-oriented, and collaborative with experience working as an integral member of a multi-site clinical trial operations team.

What You'll Do:

The key deliverables for this role are to assist and support in the planning and execution of clinical trials and research projects in accordance with designated timelines and budgets.

Manage components of projects, under the direction of senior study manager.
Assist in the preparation and oversee distribution of study documents and materials including data collection forms, manuals of operations and technical memos to research sites.
Assemble and distribute various materials, including study supplies and data collection forms, to clinical sites.
Coordinate and schedule conference calls; write and distribute meeting minutes.
Manage correspondence and project communications.
Assist in the preparation and updating of progress reports and client/study/network meeting materials.
Assist with the preparation of site or investigator training materials; participate and/or assist with trainings for clinical study staff.
Collaborate with data management team to develop and implement data collection and management strategies.
Participate in quality control activities.
Monitor risks and implement mitigation strategies.
Gather background data and information to support proposal and project efforts.

What You'll Need:

Bachelor's Degree and 3 years of experience, Master's degree and 1 years of experience, or equivalent combination of education and experience.

Skills & Abilities:

Must have experience supporting clinical trial operations. Supporting Data Coordinating Center work is preferred.
Previous experience supporting IND or regulated studies is a plus.
Proficiency with MS Word, Outlook, PowerPoint, Excel.
Demonstrated interest in health or clinical research.
Ability to work in a highly collaborative environment.
Ability to listen and communicate well both verbally and in writing.
Ability to synthesize and summarize complex information.
Ability to work independently.
Attention to detail and accuracy.
Ability to handle regular changes to priorities, interruptions to independent work due to meetings, and multiple tasks ongoing simultaneously.
Ability to have regular, reliable and predictable attendance.
Ability to travel as needed (typically less than 10%) to committee meetings, scientific meetings, project meetings, and research sites.

#LI-KV1

EEO & Pay Equity Statements:

For San Francisco, CA USA Job Postings Only: Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records. Further information is available here.

RTI accepts applications to our job openings from candidates with criminal histories or conviction records in accordance with all applicable laws, including the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

For Applicants in Massachusetts Only: 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.

The anticipated pay range for this role is listed below. Our pay ranges represent national averages and may vary by location as a geographic differential may be applied to some locations within the United States. RTI considers multiple factors when making an offer including, for example: established salary range, internal budget, business needs, and education and years of work experience possessed by the applicant. Further, salary is merely one element to our offer.

At RTI, we demonstrate our commitment to rewarding individual and team achievement through a total rewards package. This package includes (among other things) a competitive base salary, a generous paid time off policy, merit based annual increases, bonus opportunities and a robust recognition program. Other benefits include a competitive range of insurance plans (including health, dental, life, and short-term and long-term disability), access to a retirement savings program such as a 401(k) plan, paid parental leave for all parents, financial assistance with adoption expenses or infertility treatments, financial reimbursement for education and developmental opportunities, an employee assistance program, and numerous other offerings to support a healthy work-life balance.

Hiring Salary Range: $78,000 - $95,000

Apply Now

Refine Your Search

clinical study manager jobs in remote u.s.

Assistant Clinical Study Manager

Clinical Study Project Manager

Clinical Study Manager

Clinical Study Data Reviewer

Regional Clinical Study Manager

Clinical Trial Manager

Regional Clinical Study Senior Manager

Senior CTMA Manager, Regional Clinical Study Management

Central Study Coordinator I

Clinical Project Manager (US)

Clinical Research Manager

Clinical Trial Manager (Retina)

Sr Clinical Study Manager

Clinical Sample Manager

Clinical Trial Manager, Clinical Operations

Senior Clinical Research Manager

Clinical Project Manager (CRO) - Remote

Manager, Clinical Operations

Clinical Trial Associate (Associate, Rater Services)

Senior Manager / Manager, Clinical Quality

I want to receive the latest job alert for clinical study manager in remote u.s.

Related Searches

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected