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Remote Clinical Trial Internship Jobs in Decatur, GA

Impiricus

Impiricus Intern

Atlanta, GA · On-site +1

$25/hr

Atlanta, GA, New York, NY, or Remote Who We Are Impiricus is the first and only AI-powered HCP ... This is a general application for our internship program - we welcome candidates interested in ...

CryoLife

Sr. Product Manager (Remote)

Kennesaw, GA · On-site +1

$116K - $154K/yr

Support trial site selection, training, and engagement throughout clinical trials. * Develop and manage KOL cardiac and vascular surgeon relationships for the product portfolio. * Collaborate with ...

Oshi Health

Licensed Registered Dietitian

Atlanta, GA · Remote

$75K - $80K/yr

Licensed Registered Dietitian -- Clinical Reports To: Manager of RDs States we are hiring from ... Completion of an ACEND-accredited internship * Active RD or RDN license with ability to be ...

Guardianlife

Dental Standards Leader

Atlanta, GA · On-site +1

$86K - $141K/yr

Superior knowledge of dental terminology, Current Dental Terminology (CDT) codes, clinical ... Interns are not eligible for most Company benefits. Equal Employment Opportunity Guardian is an ...

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All JobsClinical Trial JobsRemote Clinical Trial Internship JobsRemote Clinical Trial Internship Jobs in Decatur, GA

Remote Clinical Trial Internship information

See Decatur, GA salary details

$11

$36

$67

How much do remote clinical trial internship jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for remote clinical trial internship in Decatur, GA is $36.78, according to ZipRecruiter salary data. Most workers in this role earn between $25.10 and $46.92 per hour, depending on experience, location, and employer.

What is the difference between Remote Clinical Trial Internship vs Remote Clinical Research Coordinator?

AspectRemote Clinical Trial InternshipRemote Clinical Research Coordinator
Required CredentialsTypically students or recent graduates; some may have relevant courseworkUsually requires a degree in health sciences or related field; certification may be preferred
Work EnvironmentRemote, often part-time or temporary; supervised by professionalsRemote or hybrid; involves coordinating trial activities and communication with sites
Employer & Industry UsagePharmaceutical companies, CROs, research institutions; entry-level rolePharmaceutical companies, CROs, hospitals; more operational responsibilities

While both roles involve clinical research, a Remote Clinical Trial Internship is typically an entry-level, temporary position for students or recent graduates gaining exposure. In contrast, a Remote Clinical Research Coordinator has more responsibilities, often requiring relevant education and certification, focusing on managing trial activities remotely or on-site.

What are the most commonly searched types of Remote Clinical Trial jobs in Decatur, GA? The most popular types of Remote Clinical Trial jobs in Decatur, GA are:
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Remote Clinical Trial Internship jobs near you

Senior Clinical Research Associate - US

Optimapharm d.o.o.

Atlanta, GA • On-site, Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted yesterday

Job description

Location: Remote
Who we are?
Optimapharm is a mid-sized, global Contract Research Organisation (CRO) turning science into hope through agile, patient-focused clinical development. We specialise in Phase I-IV clinical studies, delivering Full-Service and Functional Service Provision (FSP) solutions that help sponsors move faster and execute with confidence.
With operations in 40+ countries and 2x the patient reach of the average mid-sized CRO, we enable accelerated regulatory pathways, faster study start-up, and access to diverse patient populations worldwide. At Optimapharm, you'll contribute to meaningful clinical research while growing your career in a dynamic, people‑focused, global environment.
As our US Clinical Operations team continues to grow, we're looking for a Senior CRA who is committed to clinical excellence, passionate about mentoring others, and driven by the opportunity to help bring innovative treatments to patients faster.
At Optimapharm, you'll work on diverse and challenging studies, collaborate with experienced professionals around the world, and play a critical role in shaping the success of clinical trials - all within a culture that supports continuous growth and recognizes expertise.
What do we offer?
  • Working in a successful company that's growing and developing every day
  • Being part of a clinical research team that transforms science into hope for patients
  • International projects and professional growth
  • Company that supports life balance
  • Company with healthy culture
  • Working with a highly experienced team of clinical research professionals
  • Competitive salary
  • Competitive PTO entitlement
  • Health insurance, including vision and dental plans, to meet your and your family's needs
  • Comprehensive pension plan to maximize savings and prepare confidently for the future
  • Employee engagement programs
  • Well-being initiatives
  • Training and development program
  • Fast-paced career path progression

Who are we looking for?
Qualifications and Experience
  • University degree, preferably in medical or life sciences; nursing education or other relevant healthcare college degree
  • At least 3-5 years of independent clinical trial monitoring experience in oncology
  • High level of knowledge of ICH GCP Guidelines, knowledge of regulatory requirements and a strong interest in clinical research
  • Computer proficiency is mandatory
  • Ability to read, analyze, and interpret common scientific and technical journals
  • Excellent verbal and written communication skills
  • Very good interpersonal and negotiation skills
  • Ability to work independently, pro-active
  • Affinity to work effectively and efficiently in a matrix environment
  • A current, valid driver's license

Your responsibilities
  • Perform routine site visits independently, including pre-study, initiation, interim monitoring and closeout visits
  • Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirements
  • Independently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicable
  • Identifying and escalating potential risks and identifying retraining opportunities for site personnel
  • Preparation of corrective and preventive (CAPA) plans for issues identified during monitoring activities and pro-active follow of each, individual CAPA until timely resolution
  • Preparation of documents required for EC submissions and notifications, translation of study-related documents (where applicable), and other tasks as instructed by the supervisor
  • Independently negotiate study budgets with potential investigators/institutions and assist with the execution of site contracts as applicable
  • Administration of site payments in accordance with relevant project instructions

By joining our fast-growing and prosperous team, you will have an excellent opportunity for further personal growth and career development.
If you would be interested in joining the Optimapharm team, please send your CV and note that only shortlisted candidates who meet the requirements will be contacted for the further selection process.
Compensation is competitive and final offers will reflect each candidate's experience, skills, and qualifications.
Disclaimer: Unsolicited CVs sent to Optimapharm (Talent Acquisition Team, Hiring Managers or any other OPT employee) by recruitment agencies will not be considered for this role. Optimapharm follows a direct sourcing strategy and collaborates exclusively with selected recruitment partners when external support is required.

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