Infusion Nurse - San Antonio, TX
Page Mechanical Group, Inc., San Antonio, TX, United States
The START Center for Cancer Research ("START") is the world’s largest early-phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in the global community practices by offering
"Hope Through Access"\
to cutting edge trials throughout the United States and Europe.
We are seeking an
Infusion Nurse . The
Infusion Nurse
is responsible for providing direct patient care to individuals who are participants in research protocols that are conducted at START. The
Infusion Nurse
uses appropriate professional judgment and decision-making in planning and providing care. Nursing care is to be delivered in a manner consistent with the Standard Operating Procedures and standards of practice, and professional evidence-based standards.
Location:
San Antonio, TX
Work Schedule:
30 hour weeks, T, W, Th 7:30am – 4pm and ½ day M
Patient Care
Administer chemotherapy/immunotherapy/investigational agent to participants (inclusive of parenteral) according to the protocol and applicable regulations.
Perform study-related activities including but not limited to venipuncture, obtaining blood specimens, IV insertion, and venous access device (central line) management, ECG collection, and vital signs.
Collect biological samples according to the protocol and Standard Operating Procedures.
Educate, explain, and inform participants of study procedures.
Record data obtained according to the protocol and Standard Operating Procedures.
Use nursing assessment skills to observe participant general well-being and potential adverse events. Document events and take appropriate action as needed.
Respond to emergency situations based upon nursing standards.
Provide patient education regarding participation in a clinical trial, chemotherapy/immunotherapy/investigational agent administration and potential side effects.
Ensure that the dignity, health, safety, and welfare of participants are given the highest priority at all times.
Planning and problem-solving tasks
Prepare for clinic day ensuring necessary supplies.
Assist with entry and completion of quality standards for EHR/PQRS.
Communicating tasks
Assist with the training and mentorship of less tenured staff.
Communicate with providers regarding a change in patient status.
Communicate and interact with peers and other departments in a manner that is viewed as having a positive effect on patient services and staff morale. Interact effectively with patients/family members and demonstrate sensitivity in regards to cultural diversity, age specific needs and confidentiality.
Protocol management tasks
Work with study team to ensure that study related procedures, drug administration, labs, vital signs and ECG are completed.
Technical and quality tasks
Use skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trials.
Remain current with appropriate emergency certifications and company emergency policy and procedures.
Able to work effectively and efficiently under tight deadlines, high volumes and multiple interruptions.
Education & Experience
High School Diploma or GED.
Licensed Registered Nurse in practicing state.
Basic Life Support (BLS) certification, and AHA certified program.
Previous experience in peripheral IV insertion and management of venous access device(s).
Preferred Experience
1 year of experience.
Oncology Certified Nurse (OCN).
Clinical Trial and oncology experience.
Experience working with Microsoft Office, including Teams, Excel and Word.
Advanced Cardiac Life Support (ACLS) Certification, an AHA certified program. Can be obtained within 90 days of hire.
ONS/ONCC Chemotherapy Immunotherapy Certificate\™. Can be obtained within first year of employment.
Best-in-Class Benefits and Perks
401(k) retirement savings plan with employer match
Eligibility for an annual performance bonus, based on role and company results
Generous paid time off and paid holidays
Comprehensive medical, dental, and vision coverage and optional insurance options
Company‑paid life and disability insurance for added financial protection
Employee Assistance Program (EAP) providing confidential, no‑cost support for you and your family from day one
Flexible FSA and HSA plans to support your financial wellness
Commitment to a supportive environment that values balance, wellbeing, and flexibility
We’re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you’ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.
More About START
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world’s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of "Hope Through Access". As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda – one of the most effective cancer drugs in medical history.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.
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"Hope Through Access"\
to cutting edge trials throughout the United States and Europe.
We are seeking an
Infusion Nurse . The
Infusion Nurse
is responsible for providing direct patient care to individuals who are participants in research protocols that are conducted at START. The
Infusion Nurse
uses appropriate professional judgment and decision-making in planning and providing care. Nursing care is to be delivered in a manner consistent with the Standard Operating Procedures and standards of practice, and professional evidence-based standards.
Location:
San Antonio, TX
Work Schedule:
30 hour weeks, T, W, Th 7:30am – 4pm and ½ day M
Patient Care
Administer chemotherapy/immunotherapy/investigational agent to participants (inclusive of parenteral) according to the protocol and applicable regulations.
Perform study-related activities including but not limited to venipuncture, obtaining blood specimens, IV insertion, and venous access device (central line) management, ECG collection, and vital signs.
Collect biological samples according to the protocol and Standard Operating Procedures.
Educate, explain, and inform participants of study procedures.
Record data obtained according to the protocol and Standard Operating Procedures.
Use nursing assessment skills to observe participant general well-being and potential adverse events. Document events and take appropriate action as needed.
Respond to emergency situations based upon nursing standards.
Provide patient education regarding participation in a clinical trial, chemotherapy/immunotherapy/investigational agent administration and potential side effects.
Ensure that the dignity, health, safety, and welfare of participants are given the highest priority at all times.
Planning and problem-solving tasks
Prepare for clinic day ensuring necessary supplies.
Assist with entry and completion of quality standards for EHR/PQRS.
Communicating tasks
Assist with the training and mentorship of less tenured staff.
Communicate with providers regarding a change in patient status.
Communicate and interact with peers and other departments in a manner that is viewed as having a positive effect on patient services and staff morale. Interact effectively with patients/family members and demonstrate sensitivity in regards to cultural diversity, age specific needs and confidentiality.
Protocol management tasks
Work with study team to ensure that study related procedures, drug administration, labs, vital signs and ECG are completed.
Technical and quality tasks
Use skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trials.
Remain current with appropriate emergency certifications and company emergency policy and procedures.
Able to work effectively and efficiently under tight deadlines, high volumes and multiple interruptions.
Education & Experience
High School Diploma or GED.
Licensed Registered Nurse in practicing state.
Basic Life Support (BLS) certification, and AHA certified program.
Previous experience in peripheral IV insertion and management of venous access device(s).
Preferred Experience
1 year of experience.
Oncology Certified Nurse (OCN).
Clinical Trial and oncology experience.
Experience working with Microsoft Office, including Teams, Excel and Word.
Advanced Cardiac Life Support (ACLS) Certification, an AHA certified program. Can be obtained within 90 days of hire.
ONS/ONCC Chemotherapy Immunotherapy Certificate\™. Can be obtained within first year of employment.
Best-in-Class Benefits and Perks
401(k) retirement savings plan with employer match
Eligibility for an annual performance bonus, based on role and company results
Generous paid time off and paid holidays
Comprehensive medical, dental, and vision coverage and optional insurance options
Company‑paid life and disability insurance for added financial protection
Employee Assistance Program (EAP) providing confidential, no‑cost support for you and your family from day one
Flexible FSA and HSA plans to support your financial wellness
Commitment to a supportive environment that values balance, wellbeing, and flexibility
We’re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you’ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.
More About START
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world’s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of "Hope Through Access". As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda – one of the most effective cancer drugs in medical history.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.
#J-18808-Ljbffr