Fortrea
Clinical Research Nurse / Daytona Beach, FL (On-Site)
Fortrea, Daytona Beach, Florida, United States, 32118
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
As one of the largest Clinical Research Organizations in the world, we have four
Early Phase Clinical Research Units
in the UK and US.
We are currently seeking a
Clinical Research Nurse,
to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. Each day is different, you will be exposed to a wide variety of Therapeutic Indications and study types (ascending dose, first-in-human, food effect, drug to drug interactions, etc.)
This is a full-time,
office/clinic-based
job in
Daytona Beach, FL .
If you join us, you will work with some of the world's leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability and pharmacokinetics of a new drug.
Many Nurses are drawn to this profession because of its direct impact on patient care. If this is your case, you will not miss that working in Phase 1 trials. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you'll be involved with the latest medical technologies and treatments, witnessing their development firsthand. When the drug you worked with gets approved, you know you'll touch many patient's lives around the world.
WHAT YOU WILL DO:
You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care clinical research.
Other key responsibilities :
Ensure that the dignity, health, safety, and welfare of participants is given the highest priority at all timesBe current with appropriate emergency certifications and company emergency policy and proceduresRespond to emergency situations based upon nursing standardsUtilize skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trialsUtilize nursing assessment skills to observe participant general well-being and potential adverse events. Document adverse events and takes appropriate action as neededObtain Informed Consent and continue the ICF process by educating, explaining and informing participants of study proceduresAdminister investigational compounds (inclusive of parenteral) to participants according to the protocol and applicable regulationsPerform study related activities such as cannulation, telemetry, holters, vital signs, ECGs, venipunctureUndertake any other duties as requiredEducation / Experience:
Associates Degree or BS degree in nursing with current licensure in applicable state.CPR/AED certifiedACLS-certified preferred upon entry to role. ACLS certification maybe be gained in role if not yet certifiedAdditional experience may be substituted for education requirementsYOU NEED TO BRING...
0-1 year of related experienceAdditional experience may be substituted for education requirementsThe important thing for us is you are comfortable working in an environment that is:
Fast paced : where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.Changing priorities constantly
asking you to prioritize and adapt on the spot.Teamwork
and
people skills
are essential for the study to run smoothly.Technology based . We collect our data directly into an electronic environment.What do you get?
Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:
Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)401(K)Paid time off (PTO)Employee recognition awardsMultiple ERG's (employee resource groups)
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
As one of the largest Clinical Research Organizations in the world, we have four
Early Phase Clinical Research Units
in the UK and US.
We are currently seeking a
Clinical Research Nurse,
to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. Each day is different, you will be exposed to a wide variety of Therapeutic Indications and study types (ascending dose, first-in-human, food effect, drug to drug interactions, etc.)
This is a full-time,
office/clinic-based
job in
Daytona Beach, FL .
If you join us, you will work with some of the world's leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability and pharmacokinetics of a new drug.
Many Nurses are drawn to this profession because of its direct impact on patient care. If this is your case, you will not miss that working in Phase 1 trials. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you'll be involved with the latest medical technologies and treatments, witnessing their development firsthand. When the drug you worked with gets approved, you know you'll touch many patient's lives around the world.
WHAT YOU WILL DO:
You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care clinical research.
Other key responsibilities :
Ensure that the dignity, health, safety, and welfare of participants is given the highest priority at all timesBe current with appropriate emergency certifications and company emergency policy and proceduresRespond to emergency situations based upon nursing standardsUtilize skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trialsUtilize nursing assessment skills to observe participant general well-being and potential adverse events. Document adverse events and takes appropriate action as neededObtain Informed Consent and continue the ICF process by educating, explaining and informing participants of study proceduresAdminister investigational compounds (inclusive of parenteral) to participants according to the protocol and applicable regulationsPerform study related activities such as cannulation, telemetry, holters, vital signs, ECGs, venipunctureUndertake any other duties as requiredEducation / Experience:
Associates Degree or BS degree in nursing with current licensure in applicable state.CPR/AED certifiedACLS-certified preferred upon entry to role. ACLS certification maybe be gained in role if not yet certifiedAdditional experience may be substituted for education requirementsYOU NEED TO BRING...
0-1 year of related experienceAdditional experience may be substituted for education requirementsThe important thing for us is you are comfortable working in an environment that is:
Fast paced : where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.Changing priorities constantly
asking you to prioritize and adapt on the spot.Teamwork
and
people skills
are essential for the study to run smoothly.Technology based . We collect our data directly into an electronic environment.What do you get?
Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:
Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)401(K)Paid time off (PTO)Employee recognition awardsMultiple ERG's (employee resource groups)
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.