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Responsibilities Interpret clinical protocols and create telephone screening tools for the call center's pre-screening of patients.
Create study summaries providing a basic overview of research studies for staff reference.
Advise on inclusion/exclusion set-up and draft correspondence to subjects and primary care physicians.
Review and familiarize with all assigned studies; serve as a resource for clinical questions.
Review marketing materials and provide clinical input.
Conduct study visits with subjects, adhering to good clinical practices and FDA guidelines.
Administer informed consent, review medical histories, physical assessments, and medications.
Assess patient compliance, response to therapy, and review lab results and ECGs with provisional interpretation.
Document adverse events, conduct other visit procedures as assigned, and support on‑call responsibilities as needed.
Provide educational training to staff on informed consent, recruitment tools, and protocol requirements.
Attend investigator meetings, support patient education, and assist in writing for company communications.
Requirements
Excellent verbal and written communication skills.
Strong interpersonal and customer service skills.
Benefits Eligible employees may receive health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
Equal Opportunity Employer System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.#J-18808-
Responsibilities Interpret clinical protocols and create telephone screening tools for the call center's pre-screening of patients.
Create study summaries providing a basic overview of research studies for staff reference.
Advise on inclusion/exclusion set-up and draft correspondence to subjects and primary care physicians.
Review and familiarize with all assigned studies; serve as a resource for clinical questions.
Review marketing materials and provide clinical input.
Conduct study visits with subjects, adhering to good clinical practices and FDA guidelines.
Administer informed consent, review medical histories, physical assessments, and medications.
Assess patient compliance, response to therapy, and review lab results and ECGs with provisional interpretation.
Document adverse events, conduct other visit procedures as assigned, and support on‑call responsibilities as needed.
Provide educational training to staff on informed consent, recruitment tools, and protocol requirements.
Attend investigator meetings, support patient education, and assist in writing for company communications.
Requirements
Excellent verbal and written communication skills.
Strong interpersonal and customer service skills.
Benefits Eligible employees may receive health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
Equal Opportunity Employer System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.#J-18808-Ljbffr
N
Neier
Sub-Investigator/PA at System One Tonawanda, NY
Career Insights for Clinical Investigator
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What they do
A Clinical Investigator works on a clinical trial, and is responsible for ensuring that an investigation is conducted according to the signed investigator statement, the investigational plan, and applicable regulations; for protecting the rights, safety, and welfare of subjects under the investigator's care; and for the control of drugs under investigation. The Clinical Investigator must also meet requirements set forth by the FDA, EMA or other regulatory body. The qualifications must be outlined in a current resume and readily available for auditors.
$159,330 / year median in New York
+12% projected growth
Job Description
Job Summary Job Title:
Sub-Investigator/PA |Location:
Buffalo, New York |Hours:
40 hours per week |Compensation:
$45.00 - $65.00 per hour |Type:
Contract - 6 months with the possibility to go permOverview The Sub-Investigator, under the supervision of the Principal Investigator, is responsible for both clinical and educational aspects of clinical trial studies while focused on interpreting clinical protocols and conducting study visits with subjects.Responsibilities Interpret clinical protocols and create telephone screening tools for the call center's pre-screening of patients.
Create study summaries providing a basic overview of research studies for staff reference.
Advise on inclusion/exclusion set-up and draft correspondence to subjects and primary care physicians.
Review and familiarize with all assigned studies; serve as a resource for clinical questions.
Review marketing materials and provide clinical input.
Conduct study visits with subjects, adhering to good clinical practices and FDA guidelines.
Administer informed consent, review medical histories, physical assessments, and medications.
Assess patient compliance, response to therapy, and review lab results and ECGs with provisional interpretation.
Document adverse events, conduct other visit procedures as assigned, and support on‑call responsibilities as needed.
Provide educational training to staff on informed consent, recruitment tools, and protocol requirements.
Attend investigator meetings, support patient education, and assist in writing for company communications.
Requirements
RN, BS, NP
with NYS certification as Family or Adult NP or PA.At least five years' clinical experience.Excellent verbal and written communication skills.
Strong interpersonal and customer service skills.
Benefits Eligible employees may receive health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
Equal Opportunity Employer System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.#J-18808-
Ljbffr Job Description Job Title:
Sub-Investigator/PA |Location:
Buffalo, New York |Hours:
40 hours per week |Compensation:
$45.00 - $65.00 per hour |Type:
Contract - 6 months with the possibility to go permOverview The Sub-Investigator, under the supervision of the Principal Investigator, is responsible for both clinical and educational aspects of clinical trial studies while focused on interpreting clinical protocols and conducting study visits with subjects.Responsibilities Interpret clinical protocols and create telephone screening tools for the call center's pre-screening of patients.
Create study summaries providing a basic overview of research studies for staff reference.
Advise on inclusion/exclusion set-up and draft correspondence to subjects and primary care physicians.
Review and familiarize with all assigned studies; serve as a resource for clinical questions.
Review marketing materials and provide clinical input.
Conduct study visits with subjects, adhering to good clinical practices and FDA guidelines.
Administer informed consent, review medical histories, physical assessments, and medications.
Assess patient compliance, response to therapy, and review lab results and ECGs with provisional interpretation.
Document adverse events, conduct other visit procedures as assigned, and support on‑call responsibilities as needed.
Provide educational training to staff on informed consent, recruitment tools, and protocol requirements.
Attend investigator meetings, support patient education, and assist in writing for company communications.
Requirements
RN, BS, NP
with NYS certification as Family or Adult NP or PA.At least five years' clinical experience.Excellent verbal and written communication skills.
Strong interpersonal and customer service skills.
Benefits Eligible employees may receive health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
Equal Opportunity Employer System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.#J-18808-Ljbffr
Benefits
- Medical Leave
- 401(k) Plans
- Health Insurance
- Dental Insurance