APP Sub-InvestigatorClinical Trial Rater
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Job Location:
Mission Viejo, CA - USA
Monthly Salary:
Not Disclosed
Posted on:
3 hours ago
Vacancies:
1 Vacancy
Job Summary
The Sub-Investigator/Rater provides oversight in medical and clinical issues as requested or required. The sub-investigator works with the Principal Investigator (PI) to evaluate clinical trials and ensure that all study-related procedures are completed in accordance with Good Clinical Practices (GCP). The sub-investigator performs critical trial-related procedures and makes important trial-related decisions when delegated by the PI. Sub-investigator is engaged in the informed consent process and has a significant role in the conduct of research. This position is primarily responsible for the accurate completion of visit procedures and collection of information from study participants according to protocols and for protecting the health safety and welfare of research addition sub-investigator may also act as the study coordinator as indicated.
Essential Duties and Responsibilities:
Including but not limited to the following:
- Provides participant consultations and education in an in- or out-patient setting under the direction of the PI in charge of the clinical trial.
- Conducts study-related physical exams and follow-up visits.
- Administer semi-structured test or rater scales as per protocol not limited to CDR ADAS-COG MMSE CSSRS Cognitive Battery Test ESS and like validated scales.
- Reviews and adheres to assigned research study protocols.
- Works with the study-leading PI in evaluation and review of potential study participant eligibility.
- Maintains proper documentation in accordance with GCP.
- Ensures that all clinical activities are carried out in accordance with established research protocols and standards in compliance with all applicable laws regulations policies and procedural requirements.
- Collaborates with multidisciplinary team members.
- Reviews lab results imaging reports and other study-specific reports.
- Reviews and verifies participant medical history collected by the Wake Research Staff/Clinicians.
- Communicates with the participant as well as the participants partner/informant/caregiver.
- Attend and successfully complete all training programs in a timely manner
- Attend participate in and complete ongoing conference calls webinars required meetings and other professional development opportunities.
- Complete required necessary training Good Clinical Practice (GCP) training and any Sponsor required trainings.
- Conduct participant interviews following specific study protocols FDA GCP ICH and HIPAA Privacy guidelines.
- Maintains knowledge and education of all applicable rules regulations policies laws and guidelines respective to their field and role.
- Support site operations for community outreach recruiting efforts and participant retention
Qualifications :
Education and Training Required:
- Masters degree OR equivalent combination of relevant education training and experience.
- Licensed Advanced Practice Registered Nurse (APRN) successful completion of an accredited through the Commission on Collegiate Nursing Education (CCNE) or the Accreditation Commission for Education in Nursing Inc. (ACEN).
- Physician Assistant (PA-C) successful completion of an accredited Physician Assistant Program recognized by the Accreditation Review Commission on Education for the Physician Assistant (ARC-PA) or its predecessors.
- Current license to practice in the state of hire
- No history of license suspension or debarment in any state or by the FDA
- Must have BLS and ACLS certifications; PALS required if pediatric experience needed at site
Minimum Experience:
- Trained in phlebotomy
- Experience in bedside procedures is preferred
- 2 years of clinical practice experience is required
- 2 years of clinical research experience as a sub-investigator is preferred.
- Pediatric experience is preferred
Knowledge Skills and Abilities:
- Qualified candidates must have a minimum of 1 year experience performing psychometric rating scales in a clinical setting or for clinical trials
- Preferred: Current or previous certifications to rate the following scales: MMSE RBANS GDS-15 QoL-AD A-IADL-Q-SV SCID-5-CT MINI LSAS HAM-A/D C-SSRS MADRS MGH-ATRQ ISI CGI HDRS-17 PANSS YMRS ADAS-Cog CDR
- Solid teamwork organizational interpersonal attention to detail and problem-solving skills.
- Strong written and verbal communication skills.
- Ability to multi-task work under time constraints work independently and cooperatively with interdisciplinary teams.
- Excellent verbal and written communication skills required.
- Ability to work independently prioritize effectively and work in a team environment required.
- Sound knowledge of FDA regulations ICH-GCP and International Organization for Standardization (ISO) standards.
- Strong written and verbal communication skills.
- Strong computer skills in appropriate software and related company and Sponsor clinical systems is required.
Additional Information :
About M3:
M3 USA is at the forefront of healthcare innovation offering digital solutions across healthcare life sciences pharmaceuticals and more. Since our inception in 2000 weve seen remarkable growth fueled by our mission to utilize the internet for a healthier world and more efficient healthcare systems.
Our success is anchored in our trusted digital platforms that engage physician communities globally facilitating impactful medical education precise job placement and insightful market research. M3 USA prides itself on a dynamic and innovative work environment where every team member contributes to global health advancements.
Joining M3 USA means being part of a dedicated team striving to make a significant difference in healthcare. We provide a unique opportunity for you to be at the cutting edge of healthcare innovation shaping the future in a meaningful career. Embrace the chance to drive change with M3 USA.
Benefits:
A career opportunity with M3 Wake Research offers competitive wages and benefits such as:
- 401(k) 401(k) matching
- Dental insurance
- Disability insurance
- Employee assistance program
- Flexible spending account
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
*M3 reserves the right to change this job description to meet the business needs of the organization
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This role provides a salary of $110000.00 - $145000.00 per year.
Remote Work :
No
Employment Type :
Full-time
Key Skills
About Company
M3 USA is at the forefront of healthcare innovation, offering digital solutions across healthcare, life sciences, pharmaceuticals, and more. Since our inception in 2000, weve seen remarkable growth, fueled by our mission to utilize the internet for a healthier world and more efficien ... View more
