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Clinical Data Associate Jobs in Frederick, MD (NOW HIRING)

Description Clinical Research Associate Venesco LLC is seeking a Clinical Research Associate (CRA ... Perform source data verification (SDV). * Review informed consent documentation and study records.

Clinical Research Associate Venesco LLC is seeking a Clinical Research Associate (CRA) to provide ... Perform source data verification (SDV). * Review informed consent documentation and study records.

Through our two business units- Emmes, a full-service CRO , and Veridix AI, our technology, data ... The Clinical Research Associate (CRA) II is responsible for monitoring clinical study sites either ...

Study Start-Up Associate II

Rockville, MD · On-site +1

$34.25 - $46.75/hr

Emmes Group is transforming the future of clinical research, bringing the promise of new medical ... such as for Data Protection, Import License etc. as required. * Helps prepare and coordinate ...

Showing results 21-40

Clinical Data Associate information

See Frederick, MD salary details

$13

$38

$86

How much do clinical data associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical data associate in Frederick, MD is $38.73, according to ZipRecruiter salary data. Most workers in this role earn between $29.13 and $38.70 per hour, depending on experience, location, and employer.

What does a clinical data associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What does a clinical data associate do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

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

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What are some common challenges faced by clinical data associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

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

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

What are the most commonly searched types of Clinical Data jobs in Frederick, MD?

The most popular types of Clinical Data jobs in Frederick, MD are:

What are popular job titles related to Clinical Data Associate jobs in Frederick, MD?

For Clinical Data Associate jobs in Frederick, MD, the most frequently searched job titles are:

What cities near Frederick, MD are hiring for Clinical Data Associate jobs?

Cities near Frederick, MD with the most Clinical Data Associate job openings:

Associate Director, OBU Strategy

AstraZeneca

Gaithersburg, MD • On-site

$289K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 18 days ago


AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

23rd of 86 rated pharmaceutical


Job description

Join AstraZeneca's Oncology Business Unit (OBU) in a role where strategy meets scientific ambition. As an Associate Director, OBU Strategy, you will assist in the creation and implementation of strategies to deliver an exciting and innovative oncology pipeline. You will drive the collection of meaningful, timely, and accurate data from a wide range of internal and external sources and perform detailed analyses. Your analysis and strategic advice will drive the long-term strategy for projects across early and late-stage development and will be the foundation for investment decisions.

Accountabilities:

  • Lead the collection and analysis of data to inform project strategies and investment decisions across all stages of development

  • Deliver detailed market assessments, revenue forecasts, and asset valuations using market research and competitor insights

  • Support ongoing development of proprietary oncology focused data tools and platforms to convey opportunity and risk assessments

  • Build strong relationships, challenge ideas constructively, and drive impactful decision-making based on scientific evidence

To achieve this, it is critical you possess strong consultative and communication skills; as well as the ability to formulate cohesive strategic arguments and respectfully challenge a group of experts. This requires effective stakeholder and relationship management skills with the ability to interact and build trusted relationships. A strong scientific background and strategic analytical skills are critical for success in the role.

The role may require moderate global travel (Medical congress, Advisory boards and key internal meetings).

Essential Skills/Experience:

  • BA/BS degree

  • 5+ years of experience working in the pharma/biopharma industry or related fields

  • Familiar with the oncology drug development process and necessary scientific, commercial and strategic considerations

  • Understanding of clinical data and clinical trial design

  • Proven experience in pharmaceutical industry or consulting in which you have contributed to the global pipeline strategy e.g. market assessment, competitor analysis, forecasting

  • Analysis and fact-based decision-making

  • Working with data and/or a science research/ bio-pharmaceutical environment

  • Understanding of general business and core marketing principles and application to future healthcare market challenges

  • Able to influence without authority and establish and maintain credibility with senior audiences

  • Resourceful, motivated, decisive and proactive; must be able to manage multiple priorities in a fast-growing organization

  • Experience of setting up short- and long-term strategic plans

  • Highly intellectually capable with agility and adaptability

  • Motivated by working in a fast-paced field with clear societal impact

Preferred Qualifications:

  • Educated to PhD level in life sciences

The annual base pay for this position ranges from $193,281.60 - $289,922.40 USD annual. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours.Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles),to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base pay(as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

Why AstraZeneca?

Join a highly valued, strategic team that is fundamental in realizing the potential of our life-changing medicines. It's through our work that AstraZeneca is able to ensure the right access is provided to our transformative medicines. Working with new drugs, new digital approaches and ever-changing environments, it's crucial that we remain flexible and on top of the detail. Running, thinking and acting fast to make smart decisions and get the right medicines to patients at the right time. We're pioneering Market Access innovations: this is the place to unlock opportunities and feed our love for the challenge. United by an unrivalled passion for patients and science and always performing at the top of our game.

Ready to make a difference? Apply today!

Date Posted

03-Sep-2026

Closing Date

11-Sep-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.


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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB