The Clinical Study Recruiter is responsible for finding, screening, and documenting participants ... startup clinical lab, ranging from assembling office furniture to occasional Wal-Mart runs for ...
The Clinical Study Recruiter is responsible for finding, screening, and documenting participants ... startup clinical lab, ranging from assembling office furniture to occasional Wal-Mart runs for ...
The Clinical Study Recruiter is responsible for finding, screening, and documenting participants ... startup clinical lab, ranging from assembling office furniture to occasional Wal-Mart runs for ...
The Clinical Study Recruiter is responsible for finding, screening, and documenting participants ... startup clinical lab, ranging from assembling office furniture to occasional Wal-Mart runs for ...
Clinical Study Recruiter
Austin, TX · On-site
$14/hr
The Clinical Study Recruiter is responsible for finding, screening, and documenting participants ... startup clinical lab, ranging from assembling office furniture to occasional Wal-Mart runs for ...
Clinical Study Recruiter
Austin, TX · On-site
$14/hr
The Clinical Study Recruiter is responsible for finding, screening, and documenting participants ... startup clinical lab, ranging from assembling office furniture to occasional Wal-Mart runs for ...
Clinical Study Recruiter
Austin, TX · On-site
$14/hr
The Clinical Study Recruiter is responsible for finding, screening, and documenting participants ... startup clinical lab, ranging from assembling office furniture to occasional Wal-Mart runs for ...
Clinical Study Recruiter
Austin, TX · On-site
$14/hr
The Clinical Study Recruiter is responsible for finding, screening, and documenting participants ... startup clinical lab, ranging from assembling office furniture to occasional Wal-Mart runs for ...
Director, Clinical Operations
Boston, MA · On-site
Lead study startup, planning, execution, monitoring, and closeout activities, ensuring timelines ... Oversee Clinical Data Management and clinical trial technologies, ensuring high-quality, timely ...
Director, Clinical Operations
Boston, MA · On-site
Lead study startup, planning, execution, monitoring, and closeout activities, ensuring timelines ... Oversee Clinical Data Management and clinical trial technologies, ensuring high-quality, timely ...
In this role, you will lead global clinical trials from sourcing strategy and RFP development ... Accountable for the development of realistic detailed study startup and/or study management ...
In this role, you will lead global clinical trials from sourcing strategy and RFP development ... Accountable for the development of realistic detailed study startup and/or study management ...
In this role, you will lead global clinical trials from sourcing strategy and RFP development ... Accountable for the development of realistic detailed study startup and/or study management ...
In this role, you will lead global clinical trials from sourcing strategy and RFP development ... Accountable for the development of realistic detailed study startup and/or study management ...
Clinical Study Specialist I
Naperville, IL · On-site
$55K - $73K/yr
Clinical Study Specialist I Are you a clinical operations professional who thrives on precision ... Site Startup & Activation ("Green Light"): Manage the collection, quality control, and filing of ...
Clinical Study Specialist I
Naperville, IL · On-site
$55K - $73K/yr
Clinical Study Specialist I Are you a clinical operations professional who thrives on precision ... Site Startup & Activation ("Green Light"): Manage the collection, quality control, and filing of ...
Clinical Project Manager
Cambridge, MA · On-site
Experience managing global clinical trials and study teams across all stages (startup-closeout) of phase I-III studies and a strong working knowledge of GCP/ICH and other applicable regulations ...
Clinical Project Manager
Cambridge, MA · On-site
Experience managing global clinical trials and study teams across all stages (startup-closeout) of phase I-III studies and a strong working knowledge of GCP/ICH and other applicable regulations ...
Director, Study Start-Up
$195K - $275K/yr
Provide strategic and operational leadership for endtoend study startup activities across assigned clinical programs, ensuring timely, compliant, and highquality site activation. * Accountable for ...
Director, Study Start-Up
$195K - $275K/yr
Provide strategic and operational leadership for endtoend study startup activities across assigned clinical programs, ensuring timely, compliant, and highquality site activation. * Accountable for ...
Clinical Project Manager
Cambridge, MA · On-site
Experience managing global clinical trials and study teams across all stages (startup-closeout) of phase I-III studies and a strong working knowledge of GCP/ICH and other applicable regulations ...
Clinical Project Manager
Cambridge, MA · On-site
Experience managing global clinical trials and study teams across all stages (startup-closeout) of phase I-III studies and a strong working knowledge of GCP/ICH and other applicable regulations ...
Temporary Clinical Research Associate
Boston, MA · On-site
$45/hr
As a Temporary Clinical Research Associate , you will provide monitoring and clinical operations ... You will support assigned studies at various stages of the clinical lifecycle, including startup ...
Temporary Clinical Research Associate
Boston, MA · On-site
$45/hr
As a Temporary Clinical Research Associate , you will provide monitoring and clinical operations ... You will support assigned studies at various stages of the clinical lifecycle, including startup ...
Clinical Study Specialist I
Naperville, IL · On-site
$55K - $73K/yr
Clinical Study Specialist I Are you a clinical operations professional who thrives on precision ... Site Startup & Activation ("Green Light"): Manage the collection, quality control, and filing of ...
Clinical Study Specialist I
Naperville, IL · On-site
$55K - $73K/yr
Clinical Study Specialist I Are you a clinical operations professional who thrives on precision ... Site Startup & Activation ("Green Light"): Manage the collection, quality control, and filing of ...
Clinical Study Specialist I
Naperville, IL · On-site
Clinical Study Specialist I Are you a clinical operations professional who thrives on precision ... Site Startup & Activation ("Green Light"): Manage the collection, quality control, and filing of ...
Quick apply
Clinical Study Specialist I
Naperville, IL · On-site
Clinical Study Specialist I Are you a clinical operations professional who thrives on precision ... Site Startup & Activation ("Green Light"): Manage the collection, quality control, and filing of ...
Clinical Study Manager
Naples, FL · On-site
The ideal candidate would have experience managing clinical research studies from startup through closeout, overseeing site operations, CRO activities, data collection, investigational product ...
Clinical Study Manager
Naples, FL · On-site
The ideal candidate would have experience managing clinical research studies from startup through closeout, overseeing site operations, CRO activities, data collection, investigational product ...
Support study startup, maintenance and closeout activities. * Identify and escalate routine study issues, risks, or delays as appropriate. Clinical Documentation & Compliance * Draft, update, and ...
Support study startup, maintenance and closeout activities. * Identify and escalate routine study issues, risks, or delays as appropriate. Clinical Documentation & Compliance * Draft, update, and ...
Senior Clinical Studies Associate
Somerville, MA · On-site
$71K - $96K/yr
Support study startup, maintenance and closeout activities. * Identify and escalate routine study issues, risks, or delays as appropriate. Clinical Documentation & Compliance * Draft, update, and ...
Senior Clinical Studies Associate
Somerville, MA · On-site
$71K - $96K/yr
Support study startup, maintenance and closeout activities. * Identify and escalate routine study issues, risks, or delays as appropriate. Clinical Documentation & Compliance * Draft, update, and ...
Senior Clinical Studies Associate
Somerville, MA · On-site
$71K/yr
Support study startup, maintenance and closeout activities. * Identify and escalate routine study issues, risks, or delays as appropriate. Clinical Documentation & Compliance * Draft, update, and ...
Senior Clinical Studies Associate
Somerville, MA · On-site
$71K/yr
Support study startup, maintenance and closeout activities. * Identify and escalate routine study issues, risks, or delays as appropriate. Clinical Documentation & Compliance * Draft, update, and ...
Senior Clinical Studies Associate
$71K - $96K/yr
Support study startup, maintenance and closeout activities. * Identify and escalate routine study issues, risks, or delays as appropriate. Clinical Documentation & Compliance * Draft, update, and ...
Quick apply
Senior Clinical Studies Associate
$71K - $96K/yr
Support study startup, maintenance and closeout activities. * Identify and escalate routine study issues, risks, or delays as appropriate. Clinical Documentation & Compliance * Draft, update, and ...
Senior Clinical Studies Associate
$71K - $96K/yr
Support study startup, maintenance and closeout activities. * Identify and escalate routine study issues, risks, or delays as appropriate. Clinical Documentation & Compliance * Draft, update, and ...
Quick apply
Senior Clinical Studies Associate
$71K - $96K/yr
Support study startup, maintenance and closeout activities. * Identify and escalate routine study issues, risks, or delays as appropriate. Clinical Documentation & Compliance * Draft, update, and ...
Temporary Clinical Study Startup information
See salary details
$11.54 - $16.74
4% of jobs
$16.74 - $21.94
15% of jobs
$24.54 is the 25th percentile. Wages below this are outliers.
$21.94 - $27.14
13% of jobs
$27.14 - $32.34
8% of jobs
The median wage is $35.23 / hr.
$32.34 - $37.54
19% of jobs
$37.54 - $42.74
13% of jobs
$44.83 is the 75th percentile. Wages above this are outliers.
$42.74 - $47.95
10% of jobs
$47.95 - $53.15
5% of jobs
$53.15 - $58.35
11% of jobs
$58.35 - $63.55
1% of jobs
$63.55 - $68.75
1% of jobs
$11
$37
$68
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$14/hr
Full-time
Medical, PTO
Re-posted 6 days ago
Job description
Vivo Clinical Testing Labs is an emerging clinical testing laboratory that opened in January 2017. It is located in North Austin, Texas. The lab specializes in the testing of topical antiseptics and personal care cosmetics.
About the Position:
The Clinical Study Recruiter is responsible for finding, screening, and documenting participants for clinical trials conducted by Vivo Clinical Testing. Clinical Study Recruiters play a critical role in enabling clinical trials by building a database of willing and qualified study volunteers.Â
Major Duties:
Find clinical study volunteers to participate in testing.
Screen clinical study volunteers.
Maintain a database of clinical study volunteers.
Develop outreach efforts related to volunteer recruitment.
Interact directly with customers and study volunteers via phone, email and in person.
Interview prospective study subjects.Â
Coordinate with laboratory's Pricinipal Investigator to ensure adequate subject recruitment has been met for each study.
Maintain and improve study documentation and volunteer records such as consent forms.Â
Assist with sales, marketing, and outreach efforts as needed.
Interact with and provide detailed and accurate information to Accounting personnel.
Maintain a safe, fast-paced, and positive laboratory environment.
Assist with all the other aspects of a startup clinical lab, ranging from assembling office furniture to occasional Wal-Mart runs for office supplies.
Required Qualifications:
Good project management and time management skills.
Ability to be a self-starter and work cooperatively with others in a small-company environment.
Ability to treat at clinical study participants with respect and courtesy.
Skill and familiarity with social media.
Willingness to speak with members of the public to sign them up for testing.
Good work ethic.
Reliable transportation and safe driving history.
Desired Qualifications:
Prior experience working as a recruiter for a clinical testing lab.
Previous experience with outbound sales.
Strong project management skills.
Knowledge of, and experience with FDA Good Clinical Practice (GCP) regulations.
Experience managing and tracking outreach efforts (letters, ad campaigns, phone calls, etc.).
Strong knowledge of community outreach.
Proficiency in LibreOffice, especially Calc.
Proficiency in medical scheduling software, such as Clinical Conductor.
Compensation and Benefits:
- Pay for entry-level Clinical Study Recruiters is $14/hr. Other candidates' compensation commensurate with experience and skills.
- 2 weeks paid vacation
- Health insurance is NOT offered at this time.