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Clinical Study Startup Jobs in Georgia (NOW HIRING)

CenExel

Study Startup Specialist I

Savannah, GA · On-site

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 ...

IQVIA

CRA 1, IQVIA Biotech

Marietta, GA

$71K - $145K/yr

... clinical research studies by performing site monitoring and site management activities. In this ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...

IQVIA

CRA 1, IQVIA Biotech

Marietta, GA

$71K - $145K/yr

... clinical research studies by performing site monitoring and site management activities. In this ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...

Florence Healthcare

AI Product Manager

Atlanta, GA · On-site

... startup environment • Experience in high visibility roles managing a product portfolio, and ... Florence is a clinical trials platform that connects pharmaceutical companies and study sites to ...

Florence Healthcare

AI Product Manager

Atlanta, GA · On-site

... startup environment • Experience in high visibility roles managing a product portfolio, and ... Florence is a clinical trials platform that connects pharmaceutical companies and study sites to ...

American Oncology Network

Oncology Nurse Navigator

Macon, GA · On-site

$30.94 - $60.74/hr

Participate in screening and consenting patients for clinical trial * Assist with startup of trials to include regimen requests and requirements for blinded studies as assigned KPA 5 - Teamwork * One ...

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How much do clinical study startup jobs pay per hour?

As of Jul 28, 2026, the average hourly pay for clinical study startup in Georgia is $52.79, according to ZipRecruiter salary data. Most workers in this role earn between $42.84 and $59.47 per hour, depending on experience, location, and employer.

What is a Clinical Study Startup job?

A Clinical Study Startup job involves managing the initial phases of a clinical trial, ensuring all regulatory, ethical, and logistical requirements are met before patient enrollment begins. Responsibilities typically include submitting regulatory documents, coordinating with ethics committees, negotiating contracts, and ensuring trial sites are fully prepared. This role requires strong knowledge of clinical research regulations, timelines, and collaboration with internal and external stakeholders. Effective study startup is crucial for minimizing delays and ensuring compliance with industry standards.

What are the key skills and qualifications needed to thrive in the Clinical Study Startup position, and why are they important?

Success in a Clinical Study Startup role requires a strong understanding of clinical research processes, regulatory requirements, project management, and often a life sciences degree or related field. Familiarity with clinical trial management systems (CTMS), electronic trial master files (eTMF), and regulatory submission platforms is essential, along with certifications like GCP (Good Clinical Practice) being advantageous. Attention to detail, proactive problem-solving, and excellent organizational and communication skills help candidates excel. These qualifications ensure smooth study initiation, regulatory compliance, and effective cross-functional collaboration within demanding timelines.

What are the typical responsibilities of someone working in Clinical Study Startup?

Professionals in Clinical Study Startup are primarily responsible for coordinating and executing study initiation activities, including regulatory document collection, ethics submissions, site contracting, and start-up logistics. They work closely with investigators, sponsors, and cross-functional teams to ensure all regulatory and site requirements are met before the clinical trial begins. This role often involves tight deadlines and frequent communication with stakeholders both internally and externally. It's a fast-paced position that is ideal for individuals who enjoy detail-oriented work and project coordination in a collaborative environment.

What are the most commonly searched types of Clinical Study Startup jobs in Georgia? The most popular types of Clinical Study Startup jobs in Georgia are:
What are popular job titles related to Clinical Study Startup jobs in Georgia? For Clinical Study Startup jobs in Georgia, the most frequently searched job titles are:
What job categories do people searching Clinical Study Startup jobs in Georgia look for? The top searched job categories for Clinical Study Startup jobs in Georgia are:
What cities in Georgia are hiring for Clinical Study Startup jobs? Cities in Georgia with the most Clinical Study Startup job openings:
Clinical Study Startup jobs near you
Infographic showing various Clinical Study Startup job openings in Georgia as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, 1% Temporary, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $109,799 per year, or $52.8 per hour.
Study Startup Specialist I

Study Startup Specialist I

CenExel

Savannah, GA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 29 days ago

CenExel rating

7.5

Company rating: 7.5 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

65th of 120 rated laboratories

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:
Under moderate supervision, the Study Start Up Specialist I is responsible for initiating and implementing study start up activities for the daily operational and administrative functions of clinical study operations with a focus on project and resource management. Ensures the implementation of policies and procedures of site and regulatory agencies are met or exceeded.
Essential Responsibilities and Duties:
  • Ensures that assigned start-up activities are on track and in accordance with client and internal expectations.
  • Inventories, logs, and organizes study materials received during study start up.
  • Distributes study materials to delegated individuals while maintaining accountability for the transfer of supplies.
  • Collaborates with clinical staff to ensure that studies are conducted efficiently and are completed with the highest quality standards and outcomes.
  • Communicates with external vendors including contract research organizations, sponsors and monitors on behalf of clinical staff.
  • Review clinical study documentation in adherence to protocol, ensuring compliance.
  • Participates in for mal training of study staff prior to first subject screening.
  • 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:
  • Must be able to effectively communicate verbally and in writing.
  • Thorough understanding of clinical research terminology, good clinical practices, regulatory and ethical guidelines and regulations.
  • One year of experience in clinical research.
  • Strong customer service and client relationship skills.
  • Excellent organization and time management skills with strong ability to prioritize and multi-task across competing demands.
  • Excellent verbal/written communication skills with evidence of effective collaboration across businesses and functions.
  • High-level computer skills.

Working Conditions
  1. Indoor, Clinic and 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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