Clinical Trial Manager
$130K - $150K/yr
Associate Director, Team Lead Site Operations Location :FullyRemote Salary Range: $130,000 - $150 ... Proficiencywith clinical trial systems and tools (e.g., CTMS, eTMF, Microsoft Office ...
$130K - $150K/yr
Associate Director, Team Lead Site Operations Location :FullyRemote Salary Range: $130,000 - $150 ... Proficiencywith clinical trial systems and tools (e.g., CTMS, eTMF, Microsoft Office ...
$130K - $150K/yr
Associate Director, Team Lead Site Operations Location :FullyRemote Salary Range: $130,000 - $150 ... Proficiencywith clinical trial systems and tools (e.g., CTMS, eTMF, Microsoft Office ...
Houston, TX · On-site
$130K - $150K/yr
Role Overview: We are seeking a Clinical Trial Manager (CTM) to support our U.S. Clinical ... Associate Director, Team Lead Site Operations Location : Fully Remote Salary Range: $130,000 - $150 ...
Houston, TX · On-site
$130K - $150K/yr
Role Overview: We are seeking a Clinical Trial Manager (CTM) to support our U.S. Clinical ... Associate Director, Team Lead Site Operations Location : Fully Remote Salary Range: $130,000 - $150 ...
$120K - $135K/yr
We are seeking a Senior Clinical Research Associate (CRA) to support our Clinical Operations team ... Proficiencywith clinical trial systems and tools (e.g., CTMS, eTMF, Microsoft Office ...
New
$120K - $135K/yr
We are seeking a Senior Clinical Research Associate (CRA) to support our Clinical Operations team ... Proficiencywith clinical trial systems and tools (e.g., CTMS, eTMF, Microsoft Office ...
New
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Houston, TX · On-site
$80K - $96K/yr
Working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
Houston, TX · On-site
$80K - $96K/yr
Working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
Houston, TX · On-site
Working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
Houston, TX · On-site
Working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
Tomball, TX · On-site
Working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
Tomball, TX · On-site
Working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
Houston, TX · On-site
$79K - $93K/yr
Senior Research Administration Associate - Clinical Trial Billing and Finance Division: Pediatrics Work Arrangement: Hybrid Location: Hybrid within Greater Houston, TX Salary Range: $79,092 - $93,000 ...
Houston, TX · On-site
$79K - $93K/yr
Senior Research Administration Associate - Clinical Trial Billing and Finance Division: Pediatrics Work Arrangement: Hybrid Location: Hybrid within Greater Houston, TX Salary Range: $79,092 - $93,000 ...
Summary The Senior Research Administration Associate - Clinical Trial Billing and Finance is a pivotal role responsible for managing the financial lifecycle of industry sponsored clinical trials in ...
Summary The Senior Research Administration Associate - Clinical Trial Billing and Finance is a pivotal role responsible for managing the financial lifecycle of industry sponsored clinical trials in ...
Senior Clinical Research Associate ( home based ) (level dependent on experience) Job Purpose ... trial-related material. * Maintains tracking records for assigned sites including tracking of ...
Senior Clinical Research Associate ( home based ) (level dependent on experience) Job Purpose ... trial-related material. * Maintains tracking records for assigned sites including tracking of ...
Contract Senior Clinical Research Associate - Home-Based (US) ICON is a global healthcare ... Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Contract Senior Clinical Research Associate - Home-Based (US) ICON is a global healthcare ... Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Job Summary The Clinical Research Associate position at Medpace offers the unique opportunity to ... Opportunity for leadership positions - Lead CRA, CRA Manager, Clinical Trial Manager, Training and ...
Job Summary The Clinical Research Associate position at Medpace offers the unique opportunity to ... Opportunity for leadership positions - Lead CRA, CRA Manager, Clinical Trial Manager, Training and ...
$101K - $169K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... Ensure copies/originals (as required) site documents are available for filing in the Trial Master ...
$101K - $169K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... Ensure copies/originals (as required) site documents are available for filing in the Trial Master ...
$101K - $169K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... Ensure copies/originals (as required) site documents are available for filing in the Trial Master ...
$101K - $169K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... Ensure copies/originals (as required) site documents are available for filing in the Trial Master ...
... Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the ... Opportunity for leadership positions - Lead CRA, CRA Manager, Clinical Trial Manager, Training and ...
... Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the ... Opportunity for leadership positions - Lead CRA, CRA Manager, Clinical Trial Manager, Training and ...
Bellaire, TX · On-site
$41K - $42K/yr
Summary: The Clinical Research Nurse Practitioner/Physician Associate will be listed as a sub ... and clinical trial patients. * Coordinates multiple projects with competing priorities and ...
Quick apply
Bellaire, TX · On-site
$41K - $42K/yr
Summary: The Clinical Research Nurse Practitioner/Physician Associate will be listed as a sub ... and clinical trial patients. * Coordinates multiple projects with competing priorities and ...
Houston, TX · On-site +1
$64K - $76K/yr
Clinical Trial Development: Develop expertise in clinical trial design, protocol development, regulatory submissions, and research study implementation. * Scientific Communication: Build skills in ...
Houston, TX · On-site +1
$64K - $76K/yr
Clinical Trial Development: Develop expertise in clinical trial design, protocol development, regulatory submissions, and research study implementation. * Scientific Communication: Build skills in ...
Houston, TX · On-site +1
$64K - $76K/yr
Clinical Trial Development: Develop expertise in clinical trial design, protocol development, regulatory submissions, and research study implementation. * Scientific Communication: Build skills in ...
Houston, TX · On-site +1
$64K - $76K/yr
Clinical Trial Development: Develop expertise in clinical trial design, protocol development, regulatory submissions, and research study implementation. * Scientific Communication: Build skills in ...
Houston, TX · On-site +1
$64K - $76K/yr
Clinical Trial Development: Develop expertise in clinical trial design, protocol development, regulatory submissions, and research study implementation. * Scientific Communication: Build skills in ...
Houston, TX · On-site +1
$64K - $76K/yr
Clinical Trial Development: Develop expertise in clinical trial design, protocol development, regulatory submissions, and research study implementation. * Scientific Communication: Build skills in ...
Conroe, TX · On-site
$20 - $30/hr
Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc. * Skilled ...
Quick apply
Conroe, TX · On-site
$20 - $30/hr
Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc. * Skilled ...
$15.40 - $19.68
4% of jobs
$19.68 - $23.96
8% of jobs
$23.96 - $28.24
12% of jobs
$28.37 is the 25th percentile. Wages below this are outliers.
$28.24 - $32.52
26% of jobs
$32.52 - $36.79
18% of jobs
$38.28 is the 75th percentile. Wages above this are outliers.
$36.79 - $41.07
19% of jobs
$41.07 - $45.35
6% of jobs
$45.35 - $49.63
2% of jobs
$49.63 - $53.91
1% of jobs
$53.91 - $58.19
1% of jobs
$58.19 - $62.46
2% of jobs
$15
$35
$62
| Aspect | Clinical Trial Associate | Clinical Research Coordinator |
|---|---|---|
| Credentials | Bachelor's degree, often in life sciences; certifications like ACRP or SOCRA | Bachelor's degree in health sciences or related field; similar certifications |
| Work Environment | Pharmaceutical companies, CROs, clinical trial sites | Hospital, academic medical centers, clinical trial sites |
| Responsibilities | Assist in trial setup, data collection, regulatory compliance | Manage patient recruitment, conduct visits, data entry |
| Industry Usage | Common in pharmaceutical and biotech industries | Common in hospitals and academic research settings |
Both roles support clinical trials but differ mainly in scope and setting. Clinical Trial Associates typically work in industry settings focusing on trial logistics and compliance, while Clinical Research Coordinators often manage patient interactions and data at clinical sites. Understanding these differences helps in choosing the right career path or job search focus.
A clinical trial associate helps oversee late-stage drug trials. They design and implement the final clinical study before making reports to the FDA and other regulatory bodies. Their duties cover logistics, including ordering supplies, auditing all reports and documents, and ensuring their timely completion. They are responsible for making sure that the trial follows all ICH and GCP requirements.

$130K - $150K/yr
Full-time
Medical, Dental, Vision, Retirement
Posted 22 days ago
JoinImmaticsandshape thefuture ofcancerimmunotherapy; one patient at atime!
Immaticsis committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting ofPRAME, a target expressed in more than 50 cancers. Ourcutting-edgescience and robust clinical pipeline form the broadestPRAMEfranchise with the mostPRAMEindications and modalities, spanning TCR T-cell therapies and TCRbispecifics.
Why Join Us?
Innovative Environment:Helptopioneeradvancementsin cancer immunotherapy.
Collaborative Culture:Be part ofa diverse team dedicated to your professionalgrowth.
Global Impact:Contributeto therapies thatmakealasting impactonpatientsglobally.
Role Overview:
We are seeking a Clinical Trial Manager (CTM) to support our U.S. Clinical Operations team. The CTM will oversee site management, monitoring oversight, and clinical trial operations activities to ensure compliance with GCP, regulatory requirements, and company SOPs. In this role, you will work closely with cross-functional teams and clinical sites to drive study execution, site engagement, and operational excellence across clinical trials.
Reports to:Associate Director, Team Lead Site Operations
Location:FullyRemote
Salary Range:$130,000 - $150,000
Basic Qualifications:
Bachelor's degree in life sciences, nursing, or a related field
2+ years of experience in on-site clinical monitoring and 2+ years of Clinical Trial Manager experience within the pharmaceutical or biotechnology industry
Strong knowledge of ICH-GCP, FDA, EMA, and applicable clinical trial regulations
Demonstrated experience managing clinical trial sites, monitoring activities, and regulatory documentation
Proficiencywith clinical trial systems and tools (e.g., CTMS, eTMF, Microsoft Office)
PreferredQualifications:
Experience in oncology clinical trials or related therapeutic areas
Advanced ability to manage complex clinical operations processes and drive operational improvements
Experience leading training initiatives for CRAs and clinical trial sites
Demonstrated ability to drive quality, efficiency, and milestone achievement in fast-paced clinical environments
Experience contributing to process harmonization, innovation, and continuous improvement initiatives
Strong presentation, organizational, and cross-functional stakeholder management skills
In thisrole youwill:
Partner with Clinical Operations leadership to support clinical trial execution and monitoring activities in alignment with project goals
Lead site feasibility,selection, initiation, and greenlight activities for clinical trial sites
Develop andmaintainstudy-specific operational plans, training materials, and monitoring documentation
Oversee site management activities, including site engagement, regulatory submissions, and monitoring oversight
Review trial progress, patient recruitment, and data quality metrics, and implement actions to support study objectives
Provide guidance and oversight to CRAs, including trip report review and training support
Manage protocol and GCP deviations and contribute to continuous improvement of clinical operations processes and procedures
Travel required:up to50% travelrequired, domestically and internationally.
Qualified candidates willparticipatein a structured interview process, which includes:
An initialrecruiter phone screen (conducted via video)
A recruiter-facilitated introduction and interview with the hiring leader and key stakeholders (via video)
A final-stage interview, which may include an in-person meeting at our U.S. Headquarters in Houston, TX
What do we offer?
AtImmatics, we believe in investing in our team's health,safetyand well-being.Here'swhat you can expectif youjoinImmatics
Comprehensive Benefits:
Competitive rates forHealth, Dental, and Vision Insurance
4 weeks ofvacation,granted up front each year and prorated for firstand lastyear ofemployment.
12 company paid holidays
7daysof sick time
100%employer-paidlifeinsuranceup toat 1x annual salary, up to one hundred thousand dollars
100%employer-paidshort- andlong-Termdisabilitycoverage
401(k) withimmediateeligibilityandcompany match...
The company will match100% of your contributions upto3% of yourbase salaryfor the first two yearsof employment, 4% foryears 2-3 of employment, and up to5%of your salaryfrom the fourth year onward of continued employment.
Partiallypaidparentalleavefor eligible employees.
Additionalvoluntary employee-paidbenefits and services,includingaccident,hospitalindemnity, andcriticalillnessinsurance, as well as identitytheftprotection andpetinsurance.
Equal Employment Opportunity
We are an equal opportunity employer and are committed to building a diverse and inclusive workplace.We consider all qualified applicants for employment without regard torace, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexualorientation, gender identity or expression, national origin, ancestry, age, marital status, disability, geneticinformation, veteran status, or any other status protected by applicable law.
ReasonableAccommodations
We are committed to providing reasonableaccommodationsto individuals with disabilities and to applicants withsincerely heldreligious beliefs, practices, or observances.If yourequireassistanceoraccommodationduring theapplicationor interview process, please contact us at RecruitingUS@immatics.com.
Equal Employment Opportunity
We are an equal opportunity employer and are committed to building a diverse and inclusive workplace. We consider all qualified applicants for employment without regard torace, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexualorientation, gender identity or expression, national origin, ancestry, age, marital status, disability, geneticinformation, veteran status, or any other status protected by applicable law.
Reasonable Accommodations
We are committed to providing reasonable accommodations to individuals with disabilities and to applicants withsincerely heldreligious beliefs, practices, or observances. If you require assistance or accommodation during the application or interview process, please contact us atRecruitingUS@immatics.com.
Work Authorization
Applicants mustbe authorized towork in the United States without the need for current or future sponsorship. Visa sponsorships may beavailablefor certain roles.
Pre-Employment Requirements
Employment is contingent upon successful completion of a background check, referencechecksand pre-employment drug screening, wherepermittedby applicable law. For certain roles,additionalscreenings such as a credit check or motor vehicle record review may berequired, where job-related and consistent with business necessity.