Careers

# Ref 01. Experienced Clinical Research Coordinator

Position Overview:

We are seeking a bilingual (Spanish and English speaking), skilled and dedicated full-time clinical research coordinator to join our research team at Prime Clinical Research. The ideal candidate should have a strong background as a clinical research coordinator with expertise in phlebotomy. The clinical research coordinator will play a crucial role in providing exceptional patient care, performing phlebotomy tasks, and contributing to the smooth execution of research. This position offers an opportunity to make a meaningful impact on patients’ lives and contribute to advancements in medical research.

Key Responsibilities:

Phlebotomy Expertise: Perform venipuncture and capillary blood collection procedures with precision and care. Ensure patient comfort and safety during blood draws while maintaining sterile techniques.
Patient Care: Greet and prepare patients for medical procedures, collect relevant medical history, and explain procedures clearly. Assist healthcare professionals in patient examinations, treatments, and minor procedures.
Clinical Trials Support: Assist in the execution of clinical trials. Follow protocols, document procedures accurately, maintain compliance with regulatory requirements, and update CTMS. Collaborate with research staff to ensure smooth trial operations.
Sample Handling: Properly label, process, and transport collected blood and other samples. Ensure accurate documentation and timely delivery of samples to the appropriate laboratory or testing facility.
Administrative Tasks: Schedule appointments, manage patient records, and update electronic health records accurately and efficiently. Assist with billing and insurance processes as needed.
Patient Education: Provide patients with clear instructions for at-home care, medication administration, and follow-up appointments. Address patient questions and concerns with empathy and professionalism.
Infection Control: Adhere to strict infection control protocols to minimize the risk of cross-contamination and maintain a safe healthcare environment.
Recruitment: Assist and manage outreach to potential research subjects.

Qualifications:

High school diploma or equivalent.
Current Good Clinical Practice certification.
Certified Phlebotomy Technician (CPT) certification.
Previous experience as a clinical research coordinator, with a demonstrated proficiency in phlebotomy techniques.
Clinical trial experience is required.
IATA/DOT Dangerous Goods training preferred but not required.
Clear understanding of medical terminology and procedures.
Excellent communication skills, both verbal and written.
Strong interpersonal skills and the ability to work effectively within a multidisciplinary healthcare team.
Attention to detail and strong organizational skills.
Proficiency in using electronic health records (EHR) systems and basic office software.

Working Hours:

This is a contracted position, with an estimated 40 hours per week. The schedule includes weekdays generally within working hours of 9AM to 6PM, with opportunities for additional work on weekends as well.

Location:

Our primary office location is in Mansfield, but additional opportunities for more hours may become available as we expand across the DFW metroplex.

Benefits:

– Competitive hourly wage commensurate with experience.

Application Process:

Interested candidates are encouraged to submit their resume, and any relevant certifications to info@primeclinicalresearchinc.com. Qualified applicants will be contacted for interviews.

Join our team and become a vital part of our commitment to providing exceptional patient care and advancing medical knowledge through clinical research!

#Ref 02: Experienced Bilingual Recruitment Specialist

Position Overview:

We are seeking a bilingual (Spanish and English speaking), experienced part-time clinical research Recruitment Specialist to join our research team at Prime Clinical Research. The ideal candidate should have a strong background in clinical trial subject recruitment. The Recruitment Specialist will play a crucial role in communicating with and screening potential trial participants. This position offers an opportunity to make a meaningful impact on patients’ lives and contribute to advancements in medical research.

Key Responsibilities:

This includes creating ways to maximize the identification of subject recruitment sources, screening subjects, and referring subjects for potential study participation.

The Patient Recruitment Specialist is instrumental in assessing study subject eligibility utilizing clinical assessment skills.

Comply with all company policies, procedures, and conduct.

Strictly adhere to confidentiality and compliance standards.

Create and manage the execution of an aggressive and comprehensive recruitment/retention strategic plan for clinical trial subject recruitment.

Collaborate with internal team to evaluate and integrate innovative technologies for the successful acquisition of patients.

Effectively communicate frequently the recruitment strategy to executive management and team members.

Ensure project specific feedback is compiled and shared with management and utilized to improve patient recruitment/retention.

Conduct community outreach in person as needed at food banks, community centers, churches, etc.

Meet deadlines and expectations for subject recruitment goals pertaining to each trial.

Qualifications:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodation can be made to enable individuals with disabilities to perform the essential functions.

Minimum 2 years’ experience of patient recruitment or clinical research management.

Proven results generating successful patient recruitment strategies with a clinical research site.

Experience in coordinating online ad placements, advocacy outreach and traditional media.

General knowledge of medications, health and disease diagnoses, and medical terminology required.

A proven ability to multi-task in a rapidly changing environment.

Working Hours:

This is a contracted position, with an estimated 20 hours per week. The schedule includes weekdays generally within working hours of 9AM to 6PM, with opportunities for additional work on weekends as well.

Location:

Our primary office location is in Mansfield, but additional opportunities for more hours may become available as we expand across the DFW metroplex.

Benefits:

– Competitive hourly wage commensurate with experience.

– Quarterly bonus opportunities for achieving recruitment goals

Application Process:

Interested candidates are encouraged to submit their resume, and any relevant certifications to info@primeclinicalresearchinc.com. Qualified applicants will be contacted for interviews.

Join our team and become a vital part of our commitment to providing exceptional patient care and advancing medical knowledge through clinical research!

#Ref 03: Clinical Research Investigator (MD/DO)

Prime Clinical Research is a site network ready to help you get involved in clinical research! If you are a physician with your own practice and want to get involved in research but don’t know where to start, let us help. Our experienced team of clinical research professionals will support and guide you through the training and certification processes required to conduct clinical trials safely and successfully, including human research protections (HSP), Good Clinical Practice (GCP), and peer-to-peer training. After your training is complete, our team works to promote your research site and clinical expertise to pharmaceutical sponsors and CROs so you can begin conducting trials. If you have existing staff who want to participate in research, we train them. If you need research staff, our coordinators and nurses are happy to work with you.

Responsibilities:

Protect the safety and welfare of all trial participants.

Ensure that participants understand the potential risks, benefits, and extent of their participation in a trial.

Conduct the trial in accordance with the protocol, SOPs, and ICH GCP.

Assess and monitor subjects’ safety and wellbeing.

Maintain appropriate documentation such as source records, all IRB-approved protocol and informed consent form (ICF) versions, and original signed ICFs.

Ensure all staff conducting the trial have the necessary training and experience.

Provide necessary medical treatment to patients as needed throughout the duration of the trial.

Requirements:

Valid medical license (MD/DO)

Compensation:

Trial budgets vary widely depending on indication, number of patients enrolled, and scope of the protocol. Compensation will be mutually agreed upon prior to your participation in a study.

Contact:

To discuss this opportunity further, please email your CV and medical licensing information to info@primeclinicalresearchinc.com, and we will get back to you promptly. We look forward to hearing from you!

#Ref 04: Internship Opportunity

PRIME CLINICAL RESEARCH

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