Clinical Research Coordinator at Actalent Westminster, CO
25 an hour
Behavioral Health Market Context
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Benefits
Dental CoveragePaid Time OffHealth Insurance
Job Description
an ongoing Lyme Vaccine clinical trial. This onsite, full-time contract role offers an opportunity to contribute meaningfully to research. The ideal candidate will be comfortable working independently and serving as a primary CRN for the study.
Key Responsibilities
+ Investigational Product (IP) Administration: Safely and accurately administer investigational vaccines in accordance with study protocols and regulatory guidelines.
+ Data Management: Collect study data and enter it into electronic data capture (EDC) systems.
+ Query Resolution: Address and resolve data queries promptly.
+ Specimen Collection and Processing: Obtain biological specimens from participants, label and temporarily store them, perform initial processing like serum separation, and transport them to a lab for further analysis and storage.
+ General Support: Assist with various study-related tasks as needed to ensure smooth trial operations.
Qualifications:
+ Clinical Research Experience: Prior experience in a clinical research setting is preferred.
+ IP Administration Experience: Minimum of 1 year administering investigational products in a clinical trial setting.
+ Strong Communication Skills: Ability to interact professionally with study participants and team members.
+ Attention to Detail: High level of accuracy in documentation and protocol compliance.
Work Environment
+ This role operates during standard business hours in a dynamic, fast-paced research setting.
Job Type & Location
This is a Contract position based out of Westminster, MD.
Pay and Benefits
The pay range for this position is $25.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Westminster,MD.
Application Deadline
This position is anticipated to close on Dec 9, 2025.
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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email [email protected] (%[email protected]) for other accommodation options.
Key Responsibilities
+ Investigational Product (IP) Administration: Safely and accurately administer investigational vaccines in accordance with study protocols and regulatory guidelines.
+ Data Management: Collect study data and enter it into electronic data capture (EDC) systems.
+ Query Resolution: Address and resolve data queries promptly.
+ Specimen Collection and Processing: Obtain biological specimens from participants, label and temporarily store them, perform initial processing like serum separation, and transport them to a lab for further analysis and storage.
+ General Support: Assist with various study-related tasks as needed to ensure smooth trial operations.
Qualifications:
+ Clinical Research Experience: Prior experience in a clinical research setting is preferred.
+ IP Administration Experience: Minimum of 1 year administering investigational products in a clinical trial setting.
+ Strong Communication Skills: Ability to interact professionally with study participants and team members.
+ Attention to Detail: High level of accuracy in documentation and protocol compliance.
Work Environment
+ This role operates during standard business hours in a dynamic, fast-paced research setting.
Job Type & Location
This is a Contract position based out of Westminster, MD.
Pay and Benefits
The pay range for this position is $25.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Westminster,MD.
Application Deadline
This position is anticipated to close on Dec 9, 2025.
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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email [email protected] (%[email protected]) for other accommodation options.
Qualifications
- •IP Administration Experience: Minimum of 1 year administering investigational products in a clinical trial setting
- •Strong Communication Skills: Ability to interact professionally with study participants and team members
- •Attention to Detail: High level of accuracy in documentation and protocol compliance
Benefits
- •Pay and Benefits
- •The pay range for this position is $25.00 - $35.00/hr
- •Eligibility requirements apply to some benefits and may depend on your job classification and length of employment
- •Benefits are subject to change and may be subject to specific elections, plan, or program terms
- •Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Responsibilities
- •Job Type: Full-time (40 hours/week, Monday-Friday during standard business hours)
- •This onsite, full-time contract role offers an opportunity to contribute meaningfully to research
- •The ideal candidate will be comfortable working independently and serving as a primary CRN for the study
- •Investigational Product (IP) Administration: Safely and accurately administer investigational vaccines in accordance with study protocols and regulatory guidelines
- •Data Management: Collect study data and enter it into electronic data capture (EDC) systems
- •Query Resolution: Address and resolve data queries promptly
- •Specimen Collection and Processing: Obtain biological specimens from participants, label and temporarily store them, perform initial processing like serum separation, and transport them to a lab for further analysis and storage
- •General Support: Assist with various study-related tasks as needed to ensure smooth trial operations
- •This role operates during standard business hours in a dynamic, fast-paced research setting
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