
Clinical Research Coordinator/Patient Recruitment
Are you passionate about making a difference in the field of healthcare? Do you have a strong background in clinical research and a desire to connect patients with life-changing treatments? IQVIA is seeking a highly motivated and organized Clinical Research Coordinator/Patient Recruitment specialist to join our team. In this role, you will play a crucial role in the development and implementation of clinical trials, as well as identifying and engaging potential study participants. We are looking for candidates with a proven track record of success in clinical research, excellent communication skills, and a patient-centric mindset. If you are ready to take on a challenging and rewarding role in the ever-evolving world of clinical research, we would love to hear from you.
- Develop and implement strategies for patient recruitment and engagement in clinical trials.
- Identify potential study participants through various channels, such as medical records, referrals, and community outreach.
- Maintain accurate and up-to-date records of potential and enrolled participants.
- Screen potential participants for eligibility and assist in the informed consent process.
- Coordinate and schedule study visits for enrolled participants.
- Ensure compliance with study protocols and regulatory requirements.
- Collaborate with study team members, including physicians, nurses, and data managers, to ensure smooth and efficient conduct of the study.
- Act as a liaison between study participants, healthcare providers, and the study team.
- Monitor and track participant progress throughout the study, including collecting and recording data.
- Maintain confidentiality and adhere to ethical standards in all interactions with study participants.
- Communicate effectively with study sponsors and other external stakeholders.
- Participate in ongoing training and professional development to stay current with industry standards and best practices.
- Contribute to the development and improvement of study protocols and processes.
- Assist with the preparation and submission of study-related documents, such as regulatory submissions and progress reports.
- Adhere to all company policies and procedures, as well as applicable regulations and guidelines.
Strong Knowledge Of Fda Regulations And Ich/Gcp Guidelines.
Bachelor's Degree In A Relevant Field Such As Life Sciences, Healthcare, Or Psychology.
Minimum Of 2-3 Years Of Experience In Clinical Research Or Patient Recruitment, Preferably In A Pharmaceutical Or Cro Setting.
Excellent Communication And Interpersonal Skills, With The Ability To Effectively Interact With Patients, Healthcare Professionals, And Study Sponsors.
Detail-Oriented With Strong Organizational And Time Management Skills, Able To Manage Multiple Projects Simultaneously And Meet Tight Deadlines.
Data Management
Regulatory compliance
Site management
Clinical Trials
Patient Recruitment
Informed Consent
Study Coordination
Protocol Adherence
Patient Screening
Electronic Data Capture
Study Protocol
Communication
Emotional Intelligence
Leadership
Time management
Interpersonal Skills
creativity
Teamwork
Adaptability
Problem-Solving
Decision-making
According to JobzMall, the average salary range for a Clinical Research Coordinator/Patient Recruitment in San Antonio, TX, USA is $55,000 - $70,000 per year. This can vary depending on factors such as experience, education, and specific job responsibilities. Additionally, the salary may also be affected by the specific company and industry the individual is working in.
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IQVIA, formerly Quintiles and IMS Health, Inc., is an American multinational company serving the combined industries of health information technology and clinical research.

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