ZipRecruiter

Log In

1

Director Data Transcriber Jobs (NOW HIRING)

Bmo

Director, AI Architecture B2C

Chicago, IL · On-site

Ensures an integrated AI architecture across interdependent technology systems, data platforms ... Amazon Transcribe * Amazon Translate * Kendra Knowledge Search * Azure AI Services: * Azure AI ...

New

previous pagenext page

Showing results 21-40

All JobsHealthcare JobsHospital JobsMedical Transcription JobsDirector Data Transcriber Jobs

Director Data Transcriber information

See salary details

$13

$22

$28

How much do director data transcriber jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for director data transcriber in the United States is $22.63, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $25.00 per hour, depending on experience, location, and employer.

What cities are hiring for Director Data Transcriber jobs?

Cities with the most Director Data Transcriber job openings:

What are the most commonly searched types of Data Transcriber jobs?

The most popular types of Data Transcriber jobs are:

What states have the most Director Data Transcriber jobs?

States with the most job openings for Director Data Transcriber jobs include:

What are popular job titles related to Director Data Transcriber jobs?

For Director Data Transcriber jobs, the most frequently searched job titles are:

Director Data Transcriber jobs near you

Study Report Data Specialist - Part Time / Daytona Beach, FL (On-Site)

Daytona Beach, FL • On-site

Fortrea
Health Care and Social Assistance • 10K+ employees
Learn more about Fortreaexternal

Part-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 8 days ago

Fortrea rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

Job description

As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US.
We are currently seeking a Study Report Data Specialist / Part-Time, to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. Each day is different, you will be exposed to a wide variety of Therapeutic Indications and study types (ascending dose, first-in-human, food effect, drug to drug interactions, etc.)
This is a full-time, office/clinic-based job in Daytona Beach, FL.
If you join us, you will work with some of the world's leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability and pharmacokinetics of a new drug.
Many are drawn to this profession because of its direct impact on patient care. If this is your case, you will not miss that working in Phase 1 trials. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you'll be involved with the latest medical technologies and treatments, witnessing their development firsthand. When the drug you worked with gets approved, you know you'll touch many patient's lives around the world.
WHAT YOU WILL DO:
You will utilize your skills, knowledge, and clinical judgement for all aspects of data capture, review and quality for Phase I studies. The Clinical Data Monitor I is someone who ensures that all data and information is produced on time, in accordance with defined quality standards and meets the requirements of the business and our customers.
Key Responsibilities:
  • Transcribe study data into case report form
  • Enter data into the computer using the currently defined data management software.
  • Work in conjunction with study coordinators, quality, and project manager to ensure that case report form completion timelines are met.
  • Work with sponsors during monitoring visits to ensure all data questions and clarifications are answered.
  • Timely follow-up and resolution to all sponsor generated data queries
  • Constantly look for ways to improve the efficiency and quality of unit work processes.
  • And perform other related duties as assigned.

YOU NEED TO BRING:
  • High School Diploma or equivalent
  • 1-2 years experience specific to CRF data and case reporting, industry experience, sponsor experience
  • Clinical Research experience is preferred

The important thing for us is you are comfortable working in an environment that is:
  • Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
  • Changing priorities constantly asking you to prioritize and adapt on the spot.
  • Teamwork and people skills are essential for the study to run smoothly.
  • Technology based. We collect our data directly into an electronic environment.

What do you get?
Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:
  • Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
  • 401(K)
  • Paid time off (PTO)
  • Employee recognition awards
  • Multiple ERG's (employee resource groups)

Physical Requirements:
  • Ability to work in an upright and /or stationary position for 6-8 hours per day.
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
  • Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
  • Regular and consistent attendance.
  • Varied hours may be required.

Learn more about our EEO & Accommodations request here.

What Fortrea employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply