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Clinical Affairs Associate Jobs in Decatur, GA (NOW HIRING)

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Clinical Affairs Associate information

See Decatur, GA salary details

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How much do clinical affairs associate jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for clinical affairs associate in Decatur, GA is $30.79, according to ZipRecruiter salary data. Most workers in this role earn between $20.67 and $40.62 per hour, depending on experience, location, and employer.

What is a clinical affairs associate?

A Clinical Affairs Associate is a professional who supports clinical research and regulatory activities within healthcare or medical device organizations. Their primary responsibilities include assisting with the planning, execution, and monitoring of clinical trials, ensuring compliance with regulatory requirements, and helping prepare documentation for submissions to regulatory bodies. They often coordinate between internal teams, external vendors, and regulatory agencies to ensure the smooth progress of clinical studies. This role is crucial for ensuring that new medical products are safe, effective, and meet all necessary regulatory standards before reaching the market.

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

To thrive as a Clinical Affairs Associate, you need a solid understanding of clinical research processes, regulatory requirements, and data management, typically supported by a degree in life sciences or a related field. Familiarity with tools like electronic data capture (EDC) systems, clinical trial management systems (CTMS), and knowledge of GCP guidelines is essential. Strong attention to detail, organizational skills, and effective communication are standout soft skills in this role. These competencies ensure accurate documentation, regulatory compliance, and smooth coordination of clinical trial activities.

What are some typical challenges faced by clinical affairs associates when managing clinical trial documentation?

Clinical Affairs Associates often encounter challenges in ensuring all clinical trial documentation is accurate, up-to-date, and compliant with regulatory standards. Managing multiple studies simultaneously can lead to tight deadlines and the need for meticulous attention to detail. Effective communication with cross-functional teams, such as clinical operations, regulatory affairs, and data management, is essential to resolve discrepancies and maintain data integrity. Staying organized and keeping abreast of evolving regulatory requirements are key to overcoming these challenges.

What job categories do people searching Clinical Affairs Associate jobs in Decatur, GA look for?

The top searched job categories for Clinical Affairs Associate jobs in Decatur, GA are:

What cities near Decatur, GA are hiring for Clinical Affairs Associate jobs?

Cities near Decatur, GA with the most Clinical Affairs Associate job openings:

Infographic showing various Clinical Affairs Associate job openings in Decatur, GA as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 29% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $64,051 per year, or $30.8 per hour.

Associate Director, Medical Affairs (Rare Disease Division, Southeast)

Biocodex

Atlanta, GA โ€ข On-site

$160 - $235/hr

Other

Medical, Dental, Vision, Life, Retirement

This job post hasย expired today.ย Applications are no longer accepted.


Job description

## Associate Director, Medical Affairs (Rare Disease Division, Southeast)Candidatar-selocations: Los Angelestime type: Full-Timeposted on: Publicado ontemjob requisition id: R3374**Act with Purpose. Innovate with Care.**At Biocodex, we believe we can be global without being impersonal, demanding without being rigid, and innovative without losing sight of care. As a human-sized pharmaceutical company, we operate with high standards, a strong team mindset, and a clear ambition: to create meaningful, lasting impact. Here, you can own your role, grow your expertise, and be fully yourself. Weโ€™re not looking for cookie-cutter profiles. Weโ€™re looking for strong expertise, fresh thinking, and people who want to build something that matters.**Why This Role Matters:** The Associate Director, Medical Affairs will serve as a liaison to the medical/scientific community and will be responsible for establishing, developing, and maintaining relationships with prominent experts in pediatric neurology and in epilepsy within the geographic area of coverage. This position reports to the Director, Medical Affairs.**Associate Director, Medical Affairs****This position is REMOTE****Southeast Territory includes NC, SC, GA, AL, and FL.****Candidates must reside within the territory with preference given to those residing in Atlanta or near a major airport.****What You Will Do:**In this Role, You Willโ€ข Build, maintain, and manage professional relationships with Key External Experts (KEEs) to organize networks at state levels within their designated regionโ€ข Ensure the appropriate dissemination of clinical and scientific information regarding marketed and pipeline compounds in a timely, ethical and health care provider (HCP)-focused mannerโ€ข Implement clinical and educational strategies in collaboration with other company colleagues for designated HCPs/KEEs. This includes organizing medical and scientific training sessions, conferences and symposiums in medical centers and during scientific congresses in the USโ€ข Contribute to an efficient organization of medical communication activities for the marketed drugโ€ข Execute and support department projects as directed by the Medical Officer.โ€ข Report pharmacovigilance (PV), product quality (PQ), or medical information (MI) requests within 24 hours, per the Standard Operating Procedures for PV, PQ, and MI reportingโ€ข Ensure competitive and scientific intelligence is communicated to medical and leadership teamโ€ข Input of all KEE/HCP interactions in companyโ€™s software platform(s) in a timely manner. The minimum requirement is weekly inputโ€ข Work to pair our KEE/HCP educational and research questions with the latest emerging data in response to specific healthcare professional inquiriesโ€ข Providing clinical and value-based input into Biocodex communications and materials, as directed by Medical Officerโ€ข Medical Affairs Insights Lead with report generationโ€ข Specialty Pharmacy data generation and Medical Affairs liaisonโ€ข Standard HCP (Health Care Provider) Response Letters: organization and updatesโ€ข Recurring updates to Medical Affairs deck updatesโ€ข Medical Affairs lead on Inpatient ordering programโ€ข Medical Affairs lead reviewer for PRC (promotional review committee) and MRC (medical review committee)โ€ข Expanded geography and key HCP responsibilities**What You Bring:**โ€ข A reliable team-player with strong organizational, project management, detail oriented, and communication skillsโ€ข Proactive work styleโ€ข Ability to be resilient, flex, and adapt to internal and external changeโ€ข Work collaboratively across the organizationsโ€ข Autonomous and ability to work in fast-changing and multi-tasking environmentโ€ข Ability to manage and communicate in a scientific and medical environmentโ€ข Strong management and leadership capabilitiesโ€ข Excellent writing skillsโ€ข A valid unrestricted driverโ€™s licenseโ€ข The US Field-Based position is associated with a minimum of 60% time in the field while- customer facing.**What You Bring:*** Advanced scientific degree preferred (MD, PhD, PharmD), and will consider DNP, or clinically equivalent if appropriate experience (e.g., APRN, PA , RPh).* Solid experience of 5 years in the pharmaceutical industry (preferred) as a field-based medical position (MSL or similar) to provide strategic and scientific/medical direction to national/regional business unit functions.* Preferred experience in rare disease; and/or neurology or pediatrics.* Knowledge of FDA Regulations and Medical Affairs SOPs and Guidelines* Ability to respond appropriately to needs of key stakeholders and manage expectations; excellent project management skills and follow through Excellent data analysis skills; strong understanding of clinical databases* Excellent verbal and written communication skills, and exceptional interpersonal skills* Ability to work under deadline in a fast-paced environment with a high degree of flexibility* Excellent problem-solving skills required* Ability to effectively facilitate meetings and cross-functional teams* Project management experience (timelines, documents, reporting) preferred**Additional Information:**Full-Time Perks & Benefits: Medical, dental, vision, short- term & long-term disability, life insurance. 401K matchSalary range is $160k to $235k and based on experience Position open to people with disabilities**What You Will Find Here:**A team that truly has your back. Youโ€™ll join a workplace where trust, collaboration, and support are part of how we work every day.**Work that matters** No matter your role, you contribute to a healthcare company driven by ethics, responsibility, and high standards.**Room to grow and make an impact** Feedback, development opportunities, internal mobility, cross-functional projects, AI... youโ€™ll be in an environment that helps you grow and drive change.**Hiring is a two-way street**Weโ€™re looking for someone to join our team โ€” and youโ€™re looking for a role that truly fits. Thatโ€™s why weโ€™re transparent about who we are, how we work, and what you can expect from us.**Ready to bring meaning back to your work?****Reconnect with what really matters: people, impact, and the future.**Join us!#LI-RemoteBIOCODEX USA (Rare Disease) #J-18808-Ljbffr