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Clinical Research Data Manager Jobs in Boca Raton, FL

CenExel

Data Entry Coordinator

Hollywood, FL · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

We focus on quality people, teamwork, and highly experienced clinical research managers with a ... Transcribes data accurately and efficiently from source documents to electronic data capture.

Unicon Pharma Inc.

Clinical Research Nurse I

Miramar, FL · On-site

... Managers in all study conduct and/or participant-related matters on the clinical research unit ... Assists the PI with the review of laboratory data results for both the selection and randomization ...

Unicon Pharma Inc.

Clinical Research Nurse I

Miramar, FL · On-site

$30 - $33/hr

... Managers in all study conduct and/or participant-related matters on the clinical research unit ... Assists the PI with the review of laboratory data results for both the selection and randomization ...

Unicon Pharma Inc.

Clinical Research Nurse I

Miramar, FL · On-site

$25 - $28/hr

... Managers in all study conduct and/or participant-related matters on the clinical research unit ... Assists the PI with the review of laboratory data results for both the selection and randomization ...

CenExel

Medical Assistant (Clinical Research)

Hollywood, FL · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

CenExel is a leading nationwide clinical research site and patient network serving the life ... Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated ...

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All JobsClinical Research Data JobsClinical Research Data Manager JobsClinical Research Data Manager Jobs in Boca Raton, FL

Clinical Research Data Manager information

See Boca Raton, FL salary details

$46.5K

$101.9K

$179.4K

How much do clinical research data manager jobs pay per year?

As of Aug 13, 2026, the average yearly pay for clinical research data manager in Boca Raton, FL is $101,858.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,900.00 and $116,200.00 per year, depending on experience, location, and employer.

What are some common challenges faced by clinical research data managers during multi-site trials?

Clinical Research Data Managers often encounter challenges coordinating data collection across multiple research sites, such as ensuring consistent data entry, handling discrepancies, and maintaining data quality standards. Effective communication with site staff and timely resolution of data queries are essential to minimize delays and errors. Utilizing robust electronic data capture (EDC) systems and standardized procedures helps, but proactive problem-solving and attention to detail remain crucial for success in this role.

What is the difference between Clinical Research Data Manager vs Clinical Research Coordinator?

AspectClinical Research Data ManagerClinical Research Coordinator
Primary RoleOversees data collection, management, and quality control of clinical trial data.Coordinates daily trial activities, patient recruitment, and site management.
Required SkillsData management, database systems, regulatory compliance.Patient interaction, study protocol adherence, site coordination.
Work EnvironmentData centers, clinical trial sites, research organizations.Clinical sites, hospitals, research facilities.
Common CertificationsCDMP, SAS, or related data management certifications.GCP certification, clinical trial training.

While both roles support clinical research, the Clinical Research Data Manager focuses on data integrity and management, whereas the Clinical Research Coordinator handles trial operations and participant coordination. Understanding these differences helps in choosing the right career path or job search focus.

What are the key skills and qualifications needed to thrive as a clinical research data manager, and why are they important?

To thrive as a Clinical Research Data Manager, you need a solid background in life sciences, data management principles, and experience with clinical trial processes, often backed by a relevant bachelor's degree. Proficiency in electronic data capture (EDC) systems, database management tools like SQL, and familiarity with regulatory standards such as GCP are essential. Strong attention to detail, problem-solving abilities, and effective communication skills help ensure data integrity and smooth collaboration across research teams. These skills are crucial for maintaining high-quality, compliant data that support successful clinical trials and regulatory submissions.

What is a clinical research data manager?

A Clinical Research Data Manager is a professional responsible for collecting, organizing, and managing the data generated during clinical trials and research studies. They ensure that the data is accurate, complete, and complies with regulatory standards. Their work is crucial for the integrity of clinical research, as it allows researchers to draw valid conclusions from the study. Data managers work closely with clinical teams, statisticians, and regulatory bodies to maintain high-quality data throughout the research process.
What job categories do people searching Clinical Research Data Manager jobs in Boca Raton, FL look for? The top searched job categories for Clinical Research Data Manager jobs in Boca Raton, FL are:
What cities near Boca Raton, FL are hiring for Clinical Research Data Manager jobs? Cities near Boca Raton, FL with the most Clinical Research Data Manager job openings:
Clinical Research Data Manager jobs near you
Infographic showing various Clinical Research Data Manager job openings in Boca Raton, FL as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 16% Part Time, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $101,858 per year, or $49 per hour.

Data Entry Coordinator

CenExel

Hollywood, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 6 days ago

CenExel rating

7.5

Company rating: 7.5 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

64th of 120 rated laboratories

Job description

About Us:
Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Job Summary:
Under moderate supervision, the Data Entry Coordinator transcribes clinical research data correctly from source documents to electronic data capture following ALCOA-C principles.
Essential Responsibilities and Duties:
  • Ensures timely data entry thru department and study tracking, etc.
  • Maintains healthy professional relationships with Clinical Operations, Quality, Regulatory, CROs, Sponsors, etc., as well key clinical trial personnel.
  • Transcribes data accurately and efficiently from source documents to electronic data capture.
  • Assists in preparing for internal and external data audits along with the clinical operations/ quality/ and regulatory teams.
  • Completes training and obtains applicable certificates and access to CRFs/EDC.
  • Verifies source documents (e.g., "buddy check").
  • Assists CRCs in entering data from paper source documents to eCRFs correctly, accurately and on a timely manner for multiple clinical trials.
  • Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
  • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:
  • Minimum High School graduate or equivalent.
  • One year of data entry or related preferred.
  • Must have excellent computer skills and medical/research terminology.
  • Must be self-directed and able to work with minimal supervision.
  • Motivated to work consistently in a fast paced and rapidly changing environment.
  • Able to manage multiple projects and responsibilities.
  • Required Bilingual (English/Spanish)
  • Clinical Background and Psychiatric experience preferred

Working Conditions
  1. Indoor, Office environment.
  2. Essential physical requirements include sitting, typing, standing, and walking.
  3. Lightly active position, occasional lifting of up to 20 pounds.
  4. Reporting to work, as scheduled, is essential.
  5. On site work arrangement.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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