SQRL
Associate Director of Recruiting at SQRL
This role is focused exclusively on Oncology Clinical Research Trials.
Highlights
401k with match
15 days PTO
10 paid holidays
Great benefits including 401k with match, 15 days PTO, 10 paid holidays, and more
Focus exclusively on Oncology Clinical Research Trials
About Our Client Our client is a fast growing site network that currently has over 30 sites and constantly expanding! They focus on diversity in their trials including therapeutic areas: oncology, cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. Their sites conduct studies spanning Phases I-IV and they've been awarded for excellence in recruitment and recognized in the industry for retention, a best‑in‑class experience for patients and sponsors.
The Role The Sub-Investigator (Clinical Research NP) is responsible for oversight and execution of clinical trials that test new medications on behalf of sponsor/pharmaceutical companies. You will work in an oncology clinic to promote Good Clinical Practice and follow research protocols assigned alongside the PI. You will work along a lead Physician (Principal Investigator) have a team of skilled coordinators, managers, and assistants as well.
Responsibilities
Evaluate and screen potential subjects based on study eligibility criteria
Perform and review medical procedures in accordance with the clinical study protocol
Complete all documentation, paper and electronic
Provide oversight and ensures proper delegation of duties to appropriate staffProvide and maintain updated study related documentation
Evaluate and report safety reports, protocol noncompliance and any other protocol specific reports.
Medical management of patients on trial
Administering medications including IV
Tracking and management of adverse events
Monitoring
Qualifications
Ability to dedicate a full time schedule on site in Century City, CA
Prior experience working with Oncology research
#J-18808-Ljbffr
Highlights
401k with match
15 days PTO
10 paid holidays
Great benefits including 401k with match, 15 days PTO, 10 paid holidays, and more
Focus exclusively on Oncology Clinical Research Trials
About Our Client Our client is a fast growing site network that currently has over 30 sites and constantly expanding! They focus on diversity in their trials including therapeutic areas: oncology, cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. Their sites conduct studies spanning Phases I-IV and they've been awarded for excellence in recruitment and recognized in the industry for retention, a best‑in‑class experience for patients and sponsors.
The Role The Sub-Investigator (Clinical Research NP) is responsible for oversight and execution of clinical trials that test new medications on behalf of sponsor/pharmaceutical companies. You will work in an oncology clinic to promote Good Clinical Practice and follow research protocols assigned alongside the PI. You will work along a lead Physician (Principal Investigator) have a team of skilled coordinators, managers, and assistants as well.
Responsibilities
Evaluate and screen potential subjects based on study eligibility criteria
Perform and review medical procedures in accordance with the clinical study protocol
Complete all documentation, paper and electronic
Provide oversight and ensures proper delegation of duties to appropriate staffProvide and maintain updated study related documentation
Evaluate and report safety reports, protocol noncompliance and any other protocol specific reports.
Medical management of patients on trial
Administering medications including IV
Tracking and management of adverse events
Monitoring
Qualifications
Ability to dedicate a full time schedule on site in Century City, CA
Prior experience working with Oncology research
#J-18808-Ljbffr