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Senior Clinical Research Associate Jobs in Decatur, GA

CenExel

Clinical Research Coordinator

Decatur, GA · On-site

$23.75 - $31.50/hr

About Us: CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of ...

CenExel

Clinical Research Coordinator

Decatur, GA · On-site

$23.75 - $31.50/hr

About Us: CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of ...

Denali Health

Clinical Research Coordinator III

Atlanta, GA · On-site

$23.25 - $31/hr

Denali Health is a fast-growing clinical research organization dedicated to improving patient outcomes through innovative, high-quality clinical trials. We partner with leading physicians and ...

Eurofins Scientific

RESEARCH ASSOCIATE

Atlanta, GA

... of clinical studies. In over just 30 years, Eurofins has grown from one laboratory in Nantes ... Descripcion del empleo La principal mision del Research Associate sera la de cooperar en un ...

Cenexel

Clinical Research RN

Stone Mountain, GA · On-site

Clinical Research RN 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 ...

CenExel

Clinical Research RN

Stone Mountain, GA · On-site

Clinical Research RN 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 ...

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Senior Clinical Research Associate information

See Decatur, GA salary details

$35.1K

$92.1K

$140.1K

How much do senior clinical research associate jobs pay per year?

As of Jul 14, 2026, the average yearly pay for senior clinical research associate in Decatur, GA is $92,082.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,000.00 and $125,000.00 per year, depending on experience, location, and employer.

How much does a CRA II make at Icon?

A CRA II (Clinical Research Associate II) at Icon typically earns between $70,000 and $90,000 annually, depending on experience, location, and certifications. Compensation may also include bonuses and benefits related to clinical trial monitoring and site management.

What is the role of a senior clinical research associate?

A senior clinical research associate (CRA) oversees the conduct of clinical trials to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. They monitor trial sites, review data quality, and coordinate with investigators, often using electronic data capture systems, and typically require relevant certifications and experience in clinical research. Their role is essential for maintaining trial integrity and ensuring timely study completion.

What are the key skills and qualifications needed to thrive as a Senior Clinical Research Associate, and why are they important?

To thrive as a Senior Clinical Research Associate, you need a solid background in clinical research, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications such as ACRP or SOCRA are typically required. Strong organizational skills, attention to detail, and the ability to communicate effectively with diverse stakeholders make someone stand out in this position. These skills and qualities are vital for ensuring studies are conducted ethically, accurately, and in compliance with regulatory standards.

What is the highest paying job in clinical research?

In clinical research, senior roles such as Director of Clinical Operations or Clinical Program Manager typically have the highest salaries, often exceeding $150,000 annually. These positions require extensive experience, leadership skills, and often advanced certifications or degrees in related fields.

What Does a Senior Clinical Research Associate Do?

A senior clinical research associate (CRA) monitors clinical trials and manages team members. Your duties include leading project team meetings, running experiments, making observations, tracking results, and analyzing data. You also ensure experiments meet all clinical practice and safety standards. Qualifications for this career are a bachelor of science in a biomedical field or a bachelor of science in nursing (BSN), along with professional experience in a medical or research setting. You must have strong communication, interpersonal, leadership, and technical writing skills.

How much does a senior CRA make at Iqvia?

A Senior Clinical Research Associate (CRA) at IQVIA typically earns between $80,000 and $110,000 annually, depending on experience, location, and certifications. The role often requires monitoring clinical trials, ensuring compliance, and working with clinical data management tools.

What are some typical challenges faced by Senior Clinical Research Associates when overseeing multiple clinical trials?

Senior Clinical Research Associates (SCRAs) often manage several studies at once, which requires balancing competing deadlines, ensuring protocol compliance, and maintaining strong communication with site staff. A common challenge is ensuring consistent data quality and regulatory adherence across diverse sites, especially when trials are geographically dispersed. Effective time management, attention to detail, and proactive problem-solving are crucial for success in this role. Collaboration with project managers, investigators, and regulatory teams is also essential to ensure trials progress smoothly and meet all regulatory requirements.

What is a Senior Clinical Research Associate?

A Senior Clinical Research Associate (Senior CRA) is an experienced professional responsible for overseeing and monitoring clinical trials to ensure compliance with regulatory requirements, protocols, and good clinical practice. They often serve as a liaison between the sponsor and clinical sites, ensuring data integrity and patient safety. Senior CRAs may also mentor junior staff, manage multiple studies, and resolve complex issues that arise during trials. Their work is critical in bringing new medical treatments and devices to market safely and efficiently.
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Senior Clinical Research Associate jobs near you
Clinical Research Coordinator

Clinical Research Coordinator

CenExel

Decatur, GA • On-site

$23.75 - $31.50/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 7 hours ago

Job description

About Us:
CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process.
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:
Responsible for coordinating all aspects of clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
Essential Responsibilities and Duties:
  • Under supervision, coordinates aspects of patient involvement for complex and/or multiple studies from study initiation until study completion.
  • Organizes research information for clinical trials.
  • Observes subjects and assists with data analysis and reporting.
  • Schedules the collection of data.
  • Reviews, and reports adverse events, protocol deviations, and other unanticipated problems appropriately.
  • Monitors, and reports research data to maintain quality and compliance.
  • Performs administrative and regulatory duties related to the study as appropriate.
  • Participates in other protocol development activities.
  • Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)
  • Educates potential participants and caregivers on protocol specific details and expectations.
  • Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned).
  • Assists Clinical Trial Manager (CTM) with oversight of vendors, accounting, regulatory, client satisfaction, recruitment, quality, and trial outcomes.
  • Assists the CTM in planning, creating processes, trainings and development of staff.
  • 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:
  • Must have proper experience and demonstrate mastery of Clinical Research Coordinator I position.
  • High school graduate or equivalent; Bachelors Degree, preferred
  • CCRC certification preferred
  • 2-3 years of experience in the medical field, preferred
  • Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials.
  • Strong leadership and mentorship skills.
  • Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level.
  • Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations.
  • Works independently as well as functioning as part of a team.
  • Must be able to effectively communicate verbally and in writing.

Working Conditions
  1. Indoor, Office environment.
  2. Shift work, depending on location.
  3. Essential physical requirements include sitting, typing, standing, and walking.
  4. Lightly active position, occasional lifting of up to 20 pounds.
  5. Reporting to work, as scheduled, is essential.
  6. Overnight travel may be required for training and/or investigative meetings.

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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