Patient Care Technician
Evolution Research Group
Summary
The Patient Care Technician assists with the conduct of clinical trials through overseeing the care of clinical trial subjects while housed on unit. Assist with the collection of biological samples, perform venipuncture, electrocardiograms, tube labeling, sample processing, documenting in subject charts, and other related tasks in accordance with the doctor's written orders. In executing these responsibilities, the Patient Care Technician is guided by Good Clinical Practices (GCP), International Conference on Harmonization (ICH) guidelines, Health Insurance Portability and Accountability Act (HIPAA) and company standard operating procedures and policies.
Job description
Responsibilities:
- Perform regular safety and status checks on clinical trial subjects housed on unit as determined by physician orders.
- Perform appropriate research protocol procedures as delegated which may include but are not limited to vital signs, blood collection and processing, ECGs, and point of care laboratory tests.
- Perform basic lab procedures as delegated including but not limited to preparation of specimen tubes and labels, blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-ups.
- Ensure that biological specimens are disposed of appropriately.
- Maintain a clean, safe work environment for both fellow employees and clinical trial subjects.
- Engage the clinical trial subjects in group activities or one-on-one activities while housed on unit.
- Assure subjects have linens, toiletry items, and other sundries needed while the subject is housed on the unit.
- Serve meals and provide snacks to clinical trial subjects while subjects are housed on unit.
- Study, learn and comply with ERG site standard operating procedures, and other policies, practices and regulations where applicable.
- Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG's objectives.
Skills and Qualifications:
- High school Degree or equivalent
- One (1) year of clinical experience preferred.
- CPR Certification required.
- Phlebotomy certification (national) preferred.
- Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference on Harmonization (ICH) guidelines.
- Able to communicate with providers, co-workers, and others in a collaborative and courteous manner.
- Knowledgeable in medical terminology so as to communicate with physician office and staff.
- Able to initiate or modify behavior to achieve desired outcomes despite environmental factors, priorities, or problems that might not be well defined or that are subject to change.
- Ability to work independently and as a team player.
- Ability to organize and prioritize within a changing environment.
- Use safety/universal precautions to protect self, subjects and staff.
- Able to appropriately implement protocol and regulatory requirements in study conduct.
- Proficient in venipuncture, centrifugation, sample storage and performing electrocardiogram.
- Excellent documentation practices
- Good organizational and interpersonal skills
- Attentive to detail, good initiative and able to work with changing priorities.
Requirements
- High school Degree or equivalent
- One (1) year of clinical experience preferred.
- CPR Certification required.
- Phlebotomy certification (national) preferred.
- Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference on Harmonization (ICH) guidelines.
- Able to communicate with providers, co-workers, and others in a collaborative and courteous manner.
- Knowledgeable in medical terminology so as to communicate with physician office and staff.
- Able to initiate or modify behavior to achieve desired outcomes despite environmental factors, priorities, or problems that might not be well defined or that are subject to change.
- Ability to work independently and as a team player.
- Ability to organize and prioritize within a changing environment.
- Use safety/universal precautions to protect self, subjects and staff.
- Able to appropriately implement protocol and regulatory requirements in study conduct.
- Proficient in venipuncture, centrifugation, sample storage and performing electrocardiogram.
- Excellent documentation practices
- Good organizational and interpersonal skills
- Attentive to detail, good initiative and able to work with changing priorities.
Benefits
- Medical coverage
- Dental coverage
- Matching 401(k)
- Paid time off
Company overview
Evolution Research Group is a specialized clinical research organization (CRO) that provides comprehensive clinical trial management and research services to pharmaceutical, biotechnology, and medical device companies. The company focuses on designing, implementing, and managing clinical trials across various therapeutic areas, with particular expertise in complex and specialized medical fields. Their services encompass protocol development, site selection and management, patient recruitment, data management, regulatory compliance, and clinical monitoring. As a CRO, Evolution Research Group plays a critical role in advancing medical research by ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards. The organization typically collaborates with research sites, investigators, and sponsors to accelerate the development of new therapies and medical innovations. Their work contributes significantly to the drug development pipeline, helping to bring new treatments from laboratory research to clinical application while maintaining rigorous scientific standards and patient safety protocols.