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Clinical Data Review Pharmacist {159300}

West Jordan, UT · On-site

$65/hr

Clinical Data Review Pharmacist - Full Time (Onsite, West Jordan, UT) Location: West Jordan, UT ... patient/provider consultations. You will work in a centralized pharmacy location, supporting ...

Hispanic Alliance for Career Enhancement

NY · On-site

$83.43 - $222.48/hr

Develop and deliver training, presentations, and consultations to existing and prospective data consumers on clinical data assets, appropriate use, and analytics opportunities. * Stay current with ...

Hispanic Alliance for Career Enhancement

WI · On-site

$83.43 - $222.48/hr

Develop and deliver training, presentations, and consultations to existing and prospective data consumers on clinical data assets, appropriate use, and analytics opportunities. * Stay current with ...

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Clinical Data Consultant information

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How much do clinical data consultant jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for clinical data consultant in the United States is $44.89, according to ZipRecruiter salary data. Most workers in this role earn between $30.29 and $60.10 per hour, depending on experience, location, and employer.

What does a clinical data consultant do?

A Clinical Data Consultant specializes in managing, analyzing, and interpreting clinical data generated from medical research or clinical trials. They ensure the accuracy, integrity, and security of data collected during studies, often working with biostatisticians, clinical researchers, and regulatory teams. Their role includes designing data collection systems, validating datasets, and helping ensure compliance with regulatory standards like FDA or EMA guidelines. By providing expert insights, Clinical Data Consultants help organizations make informed decisions about drug development, patient care, and research outcomes.

What is the difference between Clinical Data Consultant vs Clinical Data Analyst?

AspectClinical Data ConsultantClinical Data Analyst
Required CredentialsBachelor's degree in life sciences, healthcare, or related field; knowledge of clinical researchBachelor's or master's in data science, statistics, or healthcare; strong analytical skills
Work EnvironmentConsulting firms, pharmaceutical companies, healthcare organizationsHospitals, research institutions, pharmaceutical companies
Employer & Industry UsageUsed for advising on clinical data management and complianceFocused on data analysis, reporting, and interpretation of clinical data

While both roles involve working with clinical data, Clinical Data Consultants primarily advise on data management and compliance strategies, whereas Clinical Data Analysts focus on analyzing and interpreting clinical data to support research and decision-making.

How does a clinical data consultant collaborate with clinical research teams during a study?

Clinical Data Consultants work closely with clinical research teams by designing data collection systems, ensuring data integrity, and providing expert guidance on regulatory compliance. They often participate in cross-functional meetings with clinical project managers, data managers, and biostatisticians to address data challenges, resolve discrepancies, and streamline workflows. This collaborative approach helps ensure that the clinical trial data is accurate, complete, and ready for analysis, directly supporting the success of the study and regulatory submissions.

What skills and qualifications are needed to be a clinical data consultant?

To thrive as a Clinical Data Consultant, you need a strong background in life sciences or healthcare, data analysis skills, and experience with clinical trial processes, often supported by a relevant degree. Familiarity with data management tools like SAS, SQL, EDC systems (e.g., Medidata, Oracle Clinical), and knowledge of regulatory standards (e.g., CDISC, FDA) are typically required. Excellent communication, problem-solving, and attention to detail are critical soft skills for effectively collaborating with stakeholders and ensuring data integrity. These skills are vital to ensure the accurate collection, analysis, and reporting of clinical data, which supports regulatory compliance and successful clinical trial outcomes.

Is clinical data analysis a good career?

Clinical data analysis is a valuable career in the healthcare and pharmaceutical industries, involving the interpretation of clinical trial data to support medical research and decision-making. It requires skills in data management, statistical software, and understanding of regulatory standards, making it a stable and growing field with demand for qualified professionals.
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Clinical Data Consultant jobs near you
Infographic showing various Clinical Data Consultant job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, and 4% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $93,381 per year, or $44.9 per hour.

Associate Director, Clinical Data Management

PTC Therapeutics

Warren, NJ • On-site

Full-time

Medical, Dental, Vision, Retirement

Re-posted 16 days ago

Job description

PTC Therapeutics is a global commercial biopharmaceutical company. For over 25 years our team has been deeply committed to a unified purpose: Extending life's moments for children and adults living with a rare disease.
At PTC, we cultivate an inclusive culture where everyone feels valued, respected, and empowered. We welcome candidates from all backgrounds to join our team, fostering a strong sense of belonging.
Visit our website to learn more about our company and culture!
Site: www.ptcbio.com
Job Description Summary:
Job Description:
Candidates local to the Warren, NJ area are strongly preferred for our flexible hybrid work model. We welcome applicants who are open to relocating to the area.
The Associate Director, Clinical Data Management is responsible for providing leadership and oversight of data management activities to ensure accuracy and consistency of clinical databases for subsequent analysis and reporting. This position has a leadership role to proactively develop plans for the utilization of EDC system processes and other clinical data applications that allow for internal control of clinical databases. This position will assist in defining Sponsor processes and procedures for maintaining clinical data and the associated QA/QC Documentation.
She/He may have supervisory responsibilities for both internal staff and external consultants. They may also manage direct reports and work cross-functionally with various internal departments and external resources on Data Management related issues.
The Associate Director, Clinical Data Management, supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate.
ESSENTIAL FUNCTIONS
Primary duties/responsibilities:
  • Ensure the data collected meets the requirements of the study objective and company quality standards.
  • Assist in the development and implementation of strategic vision for data management (DM) group.
  • Collaborate with CROs to prepare and ensure proper execution of data management plans and manage data management projects from beginning to end.
  • Work closely with Clinical Operations group, biostatisticians, SAS programmers and other staff as appropriate to design and develop data collection instruments (e.g., eCRF's) to ensure the required information is captured for statistical analysis.
  • Oversee coding review for adverse events, medical history and concomitant medications and coordinate medical monitor review and approval of medical coding
  • Lead data management activities, clinical database cleaning in EDC, data reconciliation with external vendor data, SAE reconciliation and lock activities.
  • Lead development of data management plans, data review plans, supervise database development, and reviewing and processing of clinical trial data to ensure completeness, accuracy, and consistency of clinical trials data.
  • Prepare and distribute or facilitate distribution of periodic reports of study status including, case report form (CRF) completion status, missing pages, query aging, clean patient tracker (CPT), etc.
  • Participate in cross functional team meetings, as requested, and communicate with all departments regarding project statuses/issues, provide ongoing feedback on data management workflows to increase efficiency and provide feedback to CRAs.
  • Lead interactions with outside vendors (e.g., clinical laboratories) on collection, transmittal, and transfer of study specific data.
  • Develop and update SOP's and other documents associated with the data collection, handling, and review processes, e.g., Working Instructions (WI), Best Practices Documents (BPD)to meet regulatory compliance and operational needs.
  • Participate in clinical review and validation of statistical outputs used in the preparation of final reports.
  • Mentor clinical team members by resolving problems and providing DM guidance.
  • Manage multiple and varied tasks, prioritize workload with attention to detail.
  • Understand the legal and compliance environment and drive collaboration with the Legal and Compliance team.
  • Drive the spirit of "ONE Team" across all functions by supporting a team approach to focus on our patients and customers as our top priorities.
  • Lead the completion of data management activities to meet project timelines and communicate status to respective team members.
  • Contribute to the development of outsourcing strategies and relationships with outsourcing partner and may play a role in identification of quality DM partners including coordinating the review and approval of the Master Services Agreement.
  • May manage, coach, and mentor direct reports.
  • Performs other tasks and assignments as needed and specified by management.

KNOWLEDGE/SKILLS/ABILITIES REQUIRED
* Minimum level of education and years of relevant work experience.
  • Bachelor's degree in science or related field (such as healthcare) and a minimum of 8 years of relevant progressively responsible experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions.

* Special knowledge or skills needed and/or licenses or certificates required.
  • Experience in second-line management and functional leadership.
  • Previous leadership of vendor management experience using Interactive Web Response System (IWRS), Imaging, Patient Reported Outcome (PRO) and other database technologies.
  • Highly detail oriented while maintaining work efficiency, able to prioritize activities across various projects at different study stages.
  • Knowledge of industry standards, such as the ICH guidelines, CDASH, 21 CFR Part 11, and FDA guidelines.
  • Understanding of drug development process and data operations required for the reporting of clinical trial data (e.g., data review, study reports, regulatory submissions, safety updates, etc.).
  • Strong verbal and written communication, decision-making, influencing, negotiation, and project management skills.
  • Technical skills and experience using Medidata or relational databases (e.g., Oracle RDC, InForm, Veeva EDC) and data visualization tools (e.g., Spotfire, J-Review, Business Objects).
  • Proficiency in the use of Microsoft Office Suite of tools (Word, Excel, etc.).
  • Learning agility and 'scalability' to take on increasing responsibility Excellent time management, flexibility, ability to coordinate workload and meet established deadlines.
  • Ability to influence without direct authority.
  • Demonstrated leadership ability and experience managing, coaching, and mentoring direct reports.
  • Ability to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members.
  • Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines.
  • Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects.

*Special knowledge or skills and/or licenses or certificates preferred.
  • Minimum five (5) years' experience with Medidata RAVE(EDC, R2DS/RBS, Architect).
  • Experience with Medidata RAVE.
  • Strong understanding and application of regulatory requirements and relevant data standards; CDISC knowledge and experience.
  • Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills preferred.

* Travel requirements
  • 5- 15%

Expected Base Salary Range
$163,800 - $206,200. The base salary offered will be contingent on assessment of candidate education level, background, and experience relative to the requirements of the position they are being considered for, as well as review of internal equity.
In addition to base salary, PTC employees are also eligible for short- and long-term incentives. All eligible employees may also enroll in PTC's medical, dental, vision, and retirement savings plans.
#LI-NM1
EEO Statement:
PTC Therapeutics is an equal opportunity employer. We welcome applications from all individuals, regardless of race, color, national origin, gender, age, physical characteristics, social origin, disability, religion, family status, pregnancy, sexual orientation, gender identity, gender expression, disability, veteran status or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.
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