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Clinical Data Manager Jobs in Boca Raton, FL (NOW HIRING)

Integral Rheumatology and Immunology Specialist

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RN Research Clinical Trial

Plantation, FL · On-site

$70K - $72K/yr

... data collection. Coordinate and manage multiple clinical trials from study start-up through closeout. * Screen, recruit, and enroll eligible study participants. * Obtain and document informed consent ...

Centerwell

Clinical Care Nurse - FL

West Palm Beach, FL · On-site

The Clinical Care RN plays a critical role in advancing clinical quality and supporting patients ... management. * Proficiency with electronic health records (e.g., Athena EMR), data analytics tools ...

Centerwell

Clinical Care Nurse (RN)

Sunrise, FL · On-site

The Clinical Care RN plays a critical role in advancing clinical quality and supporting patients ... management. * Proficiency with electronic health records (e.g., Athena EMR), data analytics tools ...

CenterWell

Clinical Care Nurse (RN)

Deerfield Beach, FL · On-site

... management, particularly in DM, HTN, CHF and COPD. Duties and Responsibilities : * Analyze clinical data and trends from platforms such as Athena EMR andDataHubtoidentifygaps in care related to Stars ...

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

Clinical Data Manager information

See Boca Raton, FL salary details

$18

$54

$77

How much do clinical data manager jobs pay per hour?

As of Jul 2, 2026, the average hourly pay for clinical data manager in Boca Raton, FL is $54.25, according to ZipRecruiter salary data. Most workers in this role earn between $42.88 and $64.57 per hour, depending on experience, location, and employer.

What are some common challenges Clinical Data Managers face when working on multi-site clinical trials?

Clinical Data Managers often encounter challenges such as ensuring data consistency across different sites, managing large volumes of complex data, and coordinating with site staff to resolve discrepancies. They must also stay up-to-date with regulatory requirements and ensure timely data cleaning and database lock. Effective communication and strong organizational skills are essential to navigate these complexities and maintain high data quality throughout the study.

What degree do you need to be a Clinical Data Manager?

A Clinical Data Manager typically needs at least a bachelor's degree in a health-related field such as life sciences, nursing, or health informatics. Many employers prefer candidates with a master's degree or additional certifications in clinical research or data management. Strong knowledge of database tools and regulatory standards is also important for the role.

What are the key skills and qualifications needed to thrive as a Clinical Data Manager, and why are they important?

To thrive as a Clinical Data Manager, you need a solid understanding of clinical research processes, data management principles, and a degree in life sciences, computer science, or related fields. Expertise with clinical data management systems (CDMS), electronic data capture (EDC) tools, and familiarity with regulatory standards like CDISC and GCP are typically required. Attention to detail, problem-solving abilities, and effective communication distinguish top performers in this role. These skills ensure accurate, compliant data handling and seamless collaboration across clinical research teams, which are critical for successful clinical trial outcomes.

What does a Clinical Data Manager do?

A Clinical Data Manager is responsible for collecting, validating, and managing data from clinical trials to ensure its accuracy, integrity, and compliance with regulatory standards. They design data collection systems, oversee database development, and collaborate with clinical research teams to resolve data discrepancies. By ensuring high-quality data, Clinical Data Managers play a vital role in the success of clinical trials and the development of new medical treatments.

What does a clinical data management do?

A clinical data manager is responsible for designing, implementing, and maintaining systems to collect, clean, and analyze data from clinical trials. They ensure data accuracy, integrity, and compliance with regulatory standards using tools like electronic data capture (EDC) systems. This role requires attention to detail, knowledge of Good Clinical Practice (GCP), and often involves collaboration with research teams and data analysts.

What Does a Clinical Data Manager Do?

A clinical data manager handles all the data needs of clinical trials for biotechnology and pharmaceutical companies. As a clinical data manager, your responsibilities include the research and storage of data related to clinical trials and programs. Your job duties are to collect, process, and analyze data. You must routinely evaluate your data collection and analysis processes to ensure that results are accurate and valid. You must also ensure that your work is in compliance with ethical research standards and regulations from organizations like the Food and Drug Administration (FDA).

How much does a Pfizer Clinical Data Manager make?

A Pfizer Clinical Data Manager typically earns between $80,000 and $120,000 annually, depending on experience, location, and level of responsibility. The role requires strong data management skills and familiarity with clinical trial software such as EDC systems.

What is the role of a Clinical Data Manager?

A Clinical Data Manager is responsible for designing, implementing, and maintaining systems to collect, manage, and ensure the quality of clinical trial data. They oversee data validation, perform data cleaning, and collaborate with study teams to ensure accurate and compliant data collection using tools like electronic data capture (EDC) systems. Their role is essential for supporting regulatory submissions and ensuring trial integrity.
More about Clinical Data Manager jobs
What are the most commonly searched types of Clinical Data jobs in Boca Raton, FL? The most popular types of Clinical Data jobs in Boca Raton, FL are:
What are popular job titles related to Clinical Data Manager jobs in Boca Raton, FL? For Clinical Data Manager jobs in Boca Raton, FL, the most frequently searched job titles are:
What job categories do people searching Clinical Data Manager jobs in Boca Raton, FL look for? The top searched job categories for Clinical Data Manager jobs in Boca Raton, FL are:
What cities near Boca Raton, FL are hiring for Clinical Data Manager jobs? Cities near Boca Raton, FL with the most Clinical Data Manager job openings:
Clinical Data Manager jobs near you
Clinical Research Assistant (HWD)

Clinical Research Assistant (HWD)

DermCare Management

Boca Raton, FL • On-site

Full-time

Posted 18 days ago

Job description

Clinical Research Assistant will perform work in one or all of the following areas Phlebotomy, Data Entry, and Administrative Assistant responsibilities in support of the clinical research team. The Clinical Research Assistant will assist in the management of multiple clinical trials according to the study protocol, perform collection of clinical data points, and provide seamless customer service to the patients attending the site.
Responsibilities Include but not limited to:
  • Complete training and ensure adherence of GCPs, SOPs, IATA, and HIPPA
  • Ensure compliance with all clinical trial protocols
  • Ensure compliance with Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations through OSHA, CDC, and HIPPA.
  • Assist research staff with Phase II-IV clinical trials from start through closure
  • Enter visits, patient recruitment in Real Time Clinical Trial Management System (CTMS)
  • Aid research department is meeting contracted and expected recruitment goals
  • Engage in quality assurance of all study documents and data prior to monitoring visits
  • Support central and local marketing campaigns by entering recruitment data, contacting patients and scheduling.
  • Coordinate office visits for trial participants based on the protocol
  • Perform phlebotomy, collect, process and ship clinical specimens
  • Assist in patient care visits and procedures according to protocol
  • Receive medication, confirm temperature in range and maintain temperature logs
  • Perform ECGs
  • Engage in patient recruitment
  • Assist with entry into Electronic Data Capture (EDC) data queries are resolved
  • Participate in Investigator meetings and trainings during the course of the trial
  • Generate PowerPoint presentations
  • Create and organize new patient charts, lab and other required supplies prior to the patient visit.
  • Gain access to Institutional Review Boards.
  • Maintain regulatory binders, CRFs, subject charting, and source documents
  • Maintain the Investigator Site Files
  • Assist with keeping Institutional Review Boards (IRB) documents, Electronic Data Capture (EDC) Clinical Trials Management System (CTMS) and Interactive Web Response Systems (IWRS) current
  • Will support central and local marketing campaigns by contacting potential subjects and scheduling
  • And all other duties as assigned

  • Possess a minimum of two (2) years experience in the clinical research or closely related field
  • Bachelors degree or relevant work experience.
  • Bilingual (Spanish), a plus.

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