ZipRecruiter

Log In

2

Remote Ppd Clinical Research Jobs in Decatur, GA

IQVIA

Senior Data Team Lead (Remote)

Atlanta, GA · Remote

$86K - $217K/yr

Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and ... Fully remote role - company equipment provided * Competitive salary and performance-based ...

IQVIA

Senior Data Team Lead (Remote)

Atlanta, GA · Remote

$86K - $217K/yr

Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and ... Fully remote role - company equipment provided * Competitive salary and performance-based ...

ConvaTec

Clinical Strategy Lead

Atlanta, GA · On-site +1

... and R&D colleagues. You will also build relationships with key opinion leaders and healthcare ... This is a remote role with quarterly travel to the Boston, MA area** Key Duties and ...

next page

Showing results 1-20

All JobsPpd Clinical Research JobsRemote Ppd Clinical Research JobsRemote Ppd Clinical Research Jobs in Decatur, GA

Remote Ppd Clinical Research information

See Decatur, GA salary details

$47.8K

$104.8K

$184.5K

How much do remote ppd clinical research jobs pay per year?

As of Jul 23, 2026, the average yearly pay for remote ppd clinical research in Decatur, GA is $104,796.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,100.00 and $119,600.00 per year, depending on experience, location, and employer.

What is a Remote PPD Clinical Research job?

A Remote PPD Clinical Research job involves working for PPD (Pharmaceutical Product Development), a global contract research organization, to support clinical trials and research projects from a remote location. Professionals in this role help design, manage, and monitor clinical studies to ensure compliance with protocols, regulatory standards, and data integrity. Responsibilities may include data management, coordinating with study sites, and supporting trial documentation. Working remotely allows employees to collaborate with international teams and clients while maintaining flexibility. This role is essential in advancing new treatments and therapies to market efficiently and safely.

What are the key skills and qualifications needed to thrive as a Remote PPD Clinical Research professional, and why are they important?

To excel as a Remote PPD Clinical Research professional, you need a comprehensive understanding of clinical trial processes, regulatory guidelines (such as GCP), and a relevant degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, remote monitoring tools, and certifications like ACRP or SOCRA are typically valuable. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for managing studies and collaborating with distributed teams. These competencies ensure compliance, data integrity, and the successful execution of clinical research in a remote environment.

How does working remotely as a PPD Clinical Research professional impact collaboration with on-site teams and study sites?

As a remote PPD Clinical Research professional, you will collaborate closely with on-site teams, investigators, and study coordinators through virtual communication platforms. While you may not be physically present, regular video calls, emails, and project management tools are used to maintain effective communication and ensure study protocols are followed. Adapting to different time zones and proactively addressing challenges in real-time are common aspects of the role. Strong organizational and interpersonal skills are essential for building trust and maintaining seamless coordination across dispersed teams.
What are popular job titles related to Remote Ppd Clinical Research jobs in Decatur, GA? For Remote Ppd Clinical Research jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Remote Ppd Clinical Research jobs in Decatur, GA look for? The top searched job categories for Remote Ppd Clinical Research jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Remote Ppd Clinical Research jobs? Cities near Decatur, GA with the most Remote Ppd Clinical Research job openings:
Remote Ppd Clinical Research jobs near you

Senior Clinical Research Associate - US

Optimapharm d.o.o.

Atlanta, GA • On-site, Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 14 days ago

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.

Apply