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Study Start Up Associate Jobs in Atlanta, GA (NOW HIRING)

Lead end-to-end country-level trial management , from study start-up through database lock and closeout * Serve as the primary contact for assigned clinical trials within your country * Ensure ...

Lab Coordinator/ Phlebotomist

Woodstock, GA · On-site

$15.25 - $19.25/hr

... for new study start-up * Transport samples * Provide mentoring to new hires and allow them to ... Associates degree is preferred. Bilingual (English/Spanish) skills are a plus. Required Skills:

CRC II (Onsite) - Marietta, GA

Marietta, GA · On-site

$23 - $30.50/hr

Prepare and maintain the Investigator Site File and/ or Trial Master File (TMF) for the study. * Participate in creation and review of timelines and start-up meetings (Investigator Meeting/SIV ...

Clinical Research Coordinator

Decatur, GA

$23.75 - $31.50/hr

Complete all needed activities for study start-up, including completing required training ... A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year ...

... study start-up to database lock. This also includes data support for department projects, and inquiries, unrelated to clinical studies. Responsibilities: * Lead, manage, execute end-to-end data ...

... study start-up to database lock. This also includes data support for department projects, and inquiries, unrelated to clinical studies. Responsibilities: * Lead, manage, execute end-to-end data ...

Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.; * Prepare and attend site initiation visits (SIV ...

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Study Start Up Associate information

See Atlanta, GA salary details

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How much do study start up associate jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for study start up associate in Atlanta, GA is $30.33, according to ZipRecruiter salary data. Most workers in this role earn between $20.34 and $40.00 per hour, depending on experience, location, and employer.

What is the difference between Study Start Up Associate vs Clinical Trial Coordinator?

AspectStudy Start Up AssociateClinical Trial Coordinator
Required CredentialsBachelor's degree, knowledge of regulatory requirementsBachelor's degree, familiarity with clinical procedures
Work EnvironmentRegulatory and site initiation activitiesParticipant management and site coordination
Employer & Industry UsagePharmaceuticals, biotech, CROsHospitals, research centers, CROs

The Study Start Up Associate primarily focuses on regulatory submissions, site qualification, and initiation processes, ensuring trial readiness. In contrast, the Clinical Trial Coordinator manages participant recruitment, scheduling, and data collection. Both roles are essential in clinical research but differ in their core responsibilities and focus areas.

What are popular job titles related to Study Start Up Associate jobs in Atlanta, GA?

For Study Start Up Associate jobs in Atlanta, GA, the most frequently searched job titles are:

What job categories do people searching Study Start Up Associate jobs in Atlanta, GA look for?

The top searched job categories for Study Start Up Associate jobs in Atlanta, GA are:

What cities near Atlanta, GA are hiring for Study Start Up Associate jobs?

Cities near Atlanta, GA with the most Study Start Up Associate job openings:

Infographic showing various Study Start Up Associate job openings in Atlanta, GA as of August 2026, with employment types broken down into 1% As Needed, 63% Full Time, 17% Part Time, 18% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $63,088 per year, or $30.3 per hour.

Clinical Project Lead, Oncology

Atlanta, GA • Remote


IQVIA
Health Care and Social Assistance • 10K+ employees

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 225 rated it services

People enjoy working here

Good employer

Paid breaks


$68K - $232K/yr

Full-time

Re-posted 29 days ago


Job description

In this remote role you will serve as the primary country-level leader for clinical trial delivery, ensuring studies are executed efficiently from start-up through closeout. You will oversee local trial operations, drive performance, and collaborate cross-functionally to deliver high-quality data aligned with regulatory requirements and sponsor expectations.

This role is ideal for a clinical operations professional who thrives in a fast-paced, large matrixed environment and is passionate about improving patient outcomes through clinical research.

Key Responsibilities

Clinical Trial Delivery & Oversight

  • Lead end-to-end country-level trial management, from study start-up through database lock and closeout
  • Serve as the primary contact for assigned clinical trials within your country
  • Ensure delivery of high-quality, compliant data and documentation aligned with ICH-GCP, SOPs, and regulatory standards
  • Contribute to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target

Site & Stakeholder Management

  • Partner with CRA's, Global Project Leads, and cross-functional teams to ensure successful study execution
  • Lead site feasibility, selection, and activation processes
  • Drive investigator engagement and site performance, including recruitment and retention strategies

Operational Excellence & Compliance

  • Monitor study progress through systems and reports; implement corrective and preventive actions (CAPA) when needed
  • Ensure inspection readiness through complete and accurate trial documentation (CTMS, eTMF)
  • Oversee patient safety reporting (AEs/SAEs) within required timelines

Financial & Vendor Management

  • Manage country-level budgets, forecasting, and financial tracking
  • Oversee local vendors and site payments, ensuring timely and accurate processing

Regulatory & Quality Assurance

  • Coordinate ethics and regulatory submissions/approvals in collaboration with start-up teams
  • Ensure compliance with local regulations and global standards (ICH-GCP)

What You Bring

Required Qualifications

  • Bachelor's degree in life sciences, healthcare, or related field
  • Strong knowledge of ICH-GCP, regulatory requirements, and clinical trial processes
  • Excellent communication and stakeholder management skills
  • Proficiency in clinical systems (e.g., CTMS, eTMF)
  • 3-5+ years of total trial management experience
  • Experience managing complex or early-phase trials
  • Demonstrated ability to lead cross-functional teams and drive performance

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $68,400.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US


What IQVIA employees say

Pay

Benefits

Hours and flexibility

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