Clinical Trial Liaison (CTL), Ophthalmology (Nationwide/US-Based) Serving as a value-added resource ... education, and therapeutic expertise. #LI-JD1 #LI-Remote
Clinical Trial Liaison (CTL), Ophthalmology (Nationwide/US-Based) Serving as a value-added resource ... education, and therapeutic expertise. #LI-JD1 #LI-Remote
Remote US or Canadian based. We are seeking candidates with either CAR T or Ophthalmology ... Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Remote US or Canadian based. We are seeking candidates with either CAR T or Ophthalmology ... Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Global Clinical Trial Leader
South San Francisco, CA · Remote
$80 - $89.58/hr
Job Title: Global Clinical Trial Leader Location: South San Francisco, CA Type: Contract ... Hybrid - onsite and remote Hours: Monday through Friday - Standard eight (8 AM to 4 PM or 9 AM to 5 ...
Quick apply
Global Clinical Trial Leader
South San Francisco, CA · Remote
$80 - $89.58/hr
Job Title: Global Clinical Trial Leader Location: South San Francisco, CA Type: Contract ... Hybrid - onsite and remote Hours: Monday through Friday - Standard eight (8 AM to 4 PM or 9 AM to 5 ...
Drug Supply/Clinical Trial Supply Manager
Aurora, CO · Remote
$70K - $90K/yr
Viable applicants will be required to pass a background and education verification check. Targeted ... Flexible and remote work schedules An Equal Opportunity Employer CPC provides equal employment ...
Drug Supply/Clinical Trial Supply Manager
Aurora, CO · Remote
$70K - $90K/yr
Viable applicants will be required to pass a background and education verification check. Targeted ... Flexible and remote work schedules An Equal Opportunity Employer CPC provides equal employment ...
Senior Clinical Trial Manager
Cambridge, MA · On-site +1
Perform clinical research site activities, which can include onsite or remote monitoring, co ... Qualifications & Education * Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, or ...
Senior Clinical Trial Manager
Cambridge, MA · On-site +1
Perform clinical research site activities, which can include onsite or remote monitoring, co ... Qualifications & Education * Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, or ...
Drug Supply / Clinical Trial Supply Manager
Aurora, CO · Remote
$70K - $90K/yr
Viable applicants will be required to pass a background and education verification check. Targeted ... Flexible and remote work schedules An Equal Opportunity Employer CPC provides equal employment ...
Quick apply
Drug Supply / Clinical Trial Supply Manager
Aurora, CO · Remote
$70K - $90K/yr
Viable applicants will be required to pass a background and education verification check. Targeted ... Flexible and remote work schedules An Equal Opportunity Employer CPC provides equal employment ...
Associate Director, Clinical Trial Management
San Francisco, CA · On-site +1
$179K - $200K/yr
Required: * BS/BA degree in related discipline or equivalent combination of education and ... Benefits: * A stimulating and rewarding workplace includes flexible work schedules, remote ...
Associate Director, Clinical Trial Management
San Francisco, CA · On-site +1
$179K - $200K/yr
Required: * BS/BA degree in related discipline or equivalent combination of education and ... Benefits: * A stimulating and rewarding workplace includes flexible work schedules, remote ...
Senior Clinical Trial Manager (CTM)
OR · On-site +1
Senior Clinical Trial Manager (CTM) Location: This position may be performed remotely with travel ... development Education and Professional Experience * Bachelor's degree in a scientific field ...
Senior Clinical Trial Manager (CTM)
OR · On-site +1
Senior Clinical Trial Manager (CTM) Location: This position may be performed remotely with travel ... development Education and Professional Experience * Bachelor's degree in a scientific field ...
Sr. Clinical Trial Manager, Therapeutics and Oncology
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$130K - $209K/yr
The Role The Senior Clinical Trial Manager (Sr. CTM) provides clinical trial oversight to the ... education, qualifications, certifications, experience, skills, performance, and business or ...
Sr. Clinical Trial Manager, Therapeutics and Oncology
Princeton, NJ · On-site +1
$130K - $209K/yr
The Role The Senior Clinical Trial Manager (Sr. CTM) provides clinical trial oversight to the ... education, qualifications, certifications, experience, skills, performance, and business or ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Serves as the clinical trial lead responsible for the planning, conduct and oversight of the ... Bachelor's degree or equivalent combination of education/experience in science or health-related ...
Serves as the clinical trial lead responsible for the planning, conduct and oversight of the ... Bachelor's degree or equivalent combination of education/experience in science or health-related ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work ...
Remote Clinical Trial Educator information
See salary details
$18.99 - $23.51
1% of jobs
$23.51 - $28.04
6% of jobs
$28.04 - $32.56
14% of jobs
$33.55 is the 25th percentile. Wages below this are outliers.
$32.56 - $37.08
17% of jobs
The median wage is $40.40 / hr.
$37.08 - $41.61
16% of jobs
$41.61 - $46.13
7% of jobs
$50.17 is the 75th percentile. Wages above this are outliers.
$46.13 - $50.66
15% of jobs
$50.66 - $55.18
7% of jobs
$55.18 - $59.70
7% of jobs
$59.70 - $64.23
5% of jobs
$64.23 - $68.75
3% of jobs
$18
$43
$68
How much do remote clinical trial educator jobs pay per hour?

Clinical Trial Liaison (CTL), Ophthalmology (Nationwide/US-Based)
Dallas, TX • Remote
Full-time
Posted 15 days ago
Job description
Clinical Trial Liaison (CTL), Ophthalmology (Nationwide/US-Based)
Serving as a value-added resource and extension of the Company, the Clinical Trial Liaison (CTL) will support the Company’s Ophthalmology clinical trial pipeline. The CTL will serve as a clinical trial and clinical program subject matter expert and problem solver to help study sites optimize their study performance. The CTL will work full time to help sites address challenges in study delivery that could impact the Company’s study or program goals.
This role involves compliant collaboration with KOLs, investigators, research staff members and CRO to build strong professional partnerships, provide credible scientific expertise, and serve as a field-based extension of the clinical trial team to support ongoing studies.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Site and Investigator Partnerships
- Create investigator engagement plans to support site-specific recruitment, site identification and/or selection
- Provide clinical trial liaison support to site investigators involved in sponsored studies including protocol support, screening barriers, and clinical trial recruitment and retention
- Generate feasible, time-bound, prioritized action plans to address any barriers identified at clinical sites, document the plan and meet with the sites regularly to measure progress
- Serve as a liaison to internal R&D and Clinical Operations functions to ensure the effective support of PIs
- Collection of key medical insights from PIs to inform refinement of strategies
Building Company & Pipeline Advocacy
Through compliant scientific exchange, build and maintain professional relationships with external stakeholders to expand research, company advocacy, and educational partnerships
Expertise Management and Cross Functional Support
- Maintain awareness of and access to internal and external information sources available to support high-quality scientific exchanges with HCPs
- Develop/increase knowledge of relevant medical literature and critical appraisal of scientific publications
- Maintain knowledge base and scientific expertise on all assigned disease areas and products
- Develop and update knowledge of applicable pharmaceutical guidelines and regulations. Code of Ethical Practices and company policies
- Provide scientific input and participate in local medical and cross functional initiatives
- Build scientific relationships with key thought leaders, healthcare professionals, investigators and their teams, government organizations, and patient and provider advocacy groups
- Collect key strategic insights from top research KOLs and HCPs to support strategic initiatives
- Maintain working knowledge of regulatory and ethical requirements for all initiatives.
QUALIFICATIONS:
- Knows how clinical sites operate, and has a history of helping study sites solve practical problems on clinical trials
- Healthcare/science background inclusive of PharmD, PhD and MD, OD (or equivalent) required.
- Clinical background in the area of Ophthalmology, with expertise in retinal diseases required
- 5+ years of clinical research or clinical research support experience within academic, healthcare system or industry setting (e.g., clinical research coordinator, research manager, clinical research associate, study coordinator, research director) is required. Qualified individuals will have a strong familiarity and experience with clinical research and study site logistics.
- Frequent travel is required. Availability to travel up to 50% of time
- Availability to attend meetings on holidays and weekends
- Clean and valid driver’s license
Salary offers to be determined based on industry experience, education, and therapeutic expertise.
#LI-JD1
#LI-Remote
About TMAC
Sourced by ZipRecruiter
Industry
Business management consulting
Company size
51 - 200 Employees
Headquarters location
Fort Worth, TX, US
Year founded
1995