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Remote Clinical Research Instructor Jobs in Dallas, TX

IQVIA

Senior Data Team Lead (Remote)

Dallas, TX · Remote

$86K - $217K/yr

Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and ... Fully remote role - company equipment provided * Competitive salary and performance-based ...

IQVIA

Senior Data Team Lead (Remote)

Dallas, TX · Remote

$86K - $217K/yr

Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and ... Fully remote role - company equipment provided * Competitive salary and performance-based ...

iDesign

Clinical Placement Administrator

Dallas, TX · Remote

As a Clinical Placement Administrator, you'll help support graduate and post-graduate nursing and ... Engagement Details This is a remote, part-time, hourly, 1099 independent contractor role.

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All JobsClinical Research Instructor JobsRemote Clinical Research Instructor JobsRemote Clinical Research Instructor Jobs in Dallas, TX

Remote Clinical Research Instructor information

See Dallas, TX salary details

$10.9K

$122.5K

$188.4K

How much do remote clinical research instructor jobs pay per year?

As of Aug 6, 2026, the average yearly pay for remote clinical research instructor in Dallas, TX is $122,507.00, according to ZipRecruiter salary data. Most workers in this role earn between $35,100.00 and $173,100.00 per year, depending on experience, location, and employer.

What is the difference between Remote Clinical Research Instructor vs Remote Clinical Research Coordinator?

AspectRemote Clinical Research InstructorRemote Clinical Research Coordinator
CredentialsTypically requires a clinical research certification and teaching experienceRequires clinical research certification and experience in study coordination
Work EnvironmentPrimarily online teaching, training sessions, and curriculum developmentRemote management of clinical trials, participant coordination, and data collection
Employer & IndustryEducational institutions, training companies, pharmaceutical companiesResearch sites, pharmaceutical companies, CROs
Search & Comparison IntentUnderstanding teaching roles in clinical researchUnderstanding trial management and coordination roles

The main difference is that a Remote Clinical Research Instructor focuses on educating and training others in clinical research practices, often through online courses, while a Remote Clinical Research Coordinator manages and oversees clinical trial activities remotely. Both roles require clinical research certifications but serve different functions within the industry.

What are the most commonly searched types of Clinical Research Instructor jobs in Dallas, TX? The most popular types of Clinical Research Instructor jobs in Dallas, TX are:
What are popular job titles related to Remote Clinical Research Instructor jobs in Dallas, TX? For Remote Clinical Research Instructor jobs in Dallas, TX, the most frequently searched job titles are:
What job categories do people searching Remote Clinical Research Instructor jobs in Dallas, TX look for? The top searched job categories for Remote Clinical Research Instructor jobs in Dallas, TX are:
What cities near Dallas, TX are hiring for Remote Clinical Research Instructor jobs? Cities near Dallas, TX with the most Remote Clinical Research Instructor job openings:
Remote Clinical Research Instructor jobs near you
Infographic showing various Remote Clinical Research Instructor job openings in Dallas, TX as of August 2026, with employment types broken down into 66% Full Time, 17% Part Time, and 17% Contract. Highlights an 100% Remote job distribution, with an average salary of $122,507 per year, or $58.9 per hour.

Senior Clinical Research Associate - US

Optimapharm d.o.o.

Dallas, TX • On-site, Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 29 days ago

Job description

Location: Remote
Who we are?
Optimapharm is a mid-sized, global Contract Research Organisation (CRO) turning science into hope through agile, patient-focused clinical development. We specialise in Phase I-IV clinical studies, delivering Full-Service and Functional Service Provision (FSP) solutions that help sponsors move faster and execute with confidence.
With operations in 40+ countries and 2x the patient reach of the average mid-sized CRO, we enable accelerated regulatory pathways, faster study start-up, and access to diverse patient populations worldwide. At Optimapharm, you'll contribute to meaningful clinical research while growing your career in a dynamic, people‑focused, global environment.
As our US Clinical Operations team continues to grow, we're looking for a Senior CRA who is committed to clinical excellence, passionate about mentoring others, and driven by the opportunity to help bring innovative treatments to patients faster.
At Optimapharm, you'll work on diverse and challenging studies, collaborate with experienced professionals around the world, and play a critical role in shaping the success of clinical trials - all within a culture that supports continuous growth and recognizes expertise.
What do we offer?
  • Working in a successful company that's growing and developing every day
  • Being part of a clinical research team that transforms science into hope for patients
  • International projects and professional growth
  • Company that supports life balance
  • Company with healthy culture
  • Working with a highly experienced team of clinical research professionals
  • Competitive salary
  • Competitive PTO entitlement
  • Health insurance, including vision and dental plans, to meet your and your family's needs
  • Comprehensive pension plan to maximize savings and prepare confidently for the future
  • Employee engagement programs
  • Well-being initiatives
  • Training and development program
  • Fast-paced career path progression

Who are we looking for?
Qualifications and Experience
  • University degree, preferably in medical or life sciences; nursing education or other relevant healthcare college degree
  • At least 3-5 years of independent clinical trial monitoring experience in oncology
  • High level of knowledge of ICH GCP Guidelines, knowledge of regulatory requirements and a strong interest in clinical research
  • Computer proficiency is mandatory
  • Ability to read, analyze, and interpret common scientific and technical journals
  • Excellent verbal and written communication skills
  • Very good interpersonal and negotiation skills
  • Ability to work independently, pro-active
  • Affinity to work effectively and efficiently in a matrix environment
  • A current, valid driver's license

Your responsibilities
  • Perform routine site visits independently, including pre-study, initiation, interim monitoring and closeout visits
  • Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirements
  • Independently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicable
  • Identifying and escalating potential risks and identifying retraining opportunities for site personnel
  • Preparation of corrective and preventive (CAPA) plans for issues identified during monitoring activities and pro-active follow of each, individual CAPA until timely resolution
  • Preparation of documents required for EC submissions and notifications, translation of study-related documents (where applicable), and other tasks as instructed by the supervisor
  • Independently negotiate study budgets with potential investigators/institutions and assist with the execution of site contracts as applicable
  • Administration of site payments in accordance with relevant project instructions

By joining our fast-growing and prosperous team, you will have an excellent opportunity for further personal growth and career development.
If you would be interested in joining the Optimapharm team, please send your CV and note that only shortlisted candidates who meet the requirements will be contacted for the further selection process.
Compensation is competitive and final offers will reflect each candidate's experience, skills, and qualifications.
Disclaimer: Unsolicited CVs sent to Optimapharm (Talent Acquisition Team, Hiring Managers or any other OPT employee) by recruitment agencies will not be considered for this role. Optimapharm follows a direct sourcing strategy and collaborates exclusively with selected recruitment partners when external support is required.

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