K2 Medical Research
Clinical Sub Investigator (PA / ARNP)
K2 Medical Research, Nashville, Tennessee, United States, 37247
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Clinical Sub Investigator (PA / ARNP)
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K2 Medical Research 5 days ago Be among the first 25 applicants Join to apply for the
Clinical Sub Investigator (PA / ARNP)
role at
K2 Medical Research Get AI-powered advice on this job and more exclusive features. Direct message the job poster from K2 Medical Research Strategy and Development | Marketing, HR, & Talent Management
Clinical Research Investigator
At K2 Medical Research, a privately-owned clinical research facility with multiple locations in Florida, Tennessee, and Rhode Island. We specialize in conducting multiphasic clinical trials that promote the development of innovative and effective medical treatments while maintaining the safety and privacy of our participants. Here at K2, we are committed to fighting the diseases that plague our loved ones and ourselves. By harnessing the power of advanced clinical research and connecting our patients with the treatments of tomorrow, we can improve the health of our local communities, and by extent, the population of our world.
We are seeking a
PA/ARNP/Sub Investigator for our Nashville clinic.
The Sub Investigator promotes Good Clinical Practice in the conduct of clinical investigations by ensuring adherence to protocol requirements, protecting the rights and welfare of study subjects, assuring the integrity of data generated at the site and directing the conduct of the clinical investigation according to federal and state regulations and guidance documents.
Primary Responsibilities
Provide investigator qualifications and agreements as required for study participation Maintain current, up-to-date curriculum vitae Maintain current licensure and continuing education Assume responsibility for the conduct of the clinical investigation Maintaining documentation of all aspects of the clinical investigation Ensure protocol compliance Ensure initial and ongoing review and oversight by a duly constituted IRB Provide adequate facilities to conduct the clinical trial Manage the medical care of study participants (subjects) Ensure validity of data reported to sponsor Ensure documentation of study-related procedures, processes, and events Ensure proper use, storage, and return or disposal of investigational agents Maintain professional and technical knowledge Reading, understanding and adhering to organizational Standard Operating Procedures Assisting in establishing and enforcing departmental standards Contributes to team effort by: Exploring new opportunities to add value to organization and departmental processes Helping others to achieve results Performing other duties as assigned Learns and maintains Technical and Industry Knowledge by Attending and participating in applicable company-sponsored training
Knowledge, Skills, And Abilities
Bachelor's degree in a health-related field Broad knowledge of general medicine and medical terminology Strong analytical and problem-solving skills Excellent organizational skills, detail oriented, efficient, and able to multi-task and prioritize effectively. Excellent interpersonal skills. BLS and/or ACLS Strong written and verbal communication skills. Bilingual skills preferred. Applicants that do not meet 100% of the above qualifications but who have a combination of related education and applicable experience may be considered upon approval
Qualifications
Licensed PA/ARNP/DNP in the state of TN
We value our employees and their professional and personal needs, and support these through our benefit offerings:
Benefits
Medical, Dental, Vision, Flexible Spending Accounts, Employer paid Long-Term disability and Life Insurance, Short Term Disability, Accident and Critical Illness Insurance, Voluntary Life and Long-Term Care Insurance, Legal Shield, Employee Assistance Program, and various discount programs. 401(K) Plans- Traditional and Roth plans are available; 4% employer match that is immediately vested PTO of 16 days per year, 17 days after the first year of FT employment 9 paid Holidays K2 observes a four-day work week, Monday through Thursday, for full time employees. Fridays are non-working days unless required by business needs.
Seniority level
Seniority level Entry level Employment type
Employment type Full-time Job function
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Clinical Sub Investigator (PA / ARNP)
role at
K2 Medical Research 5 days ago Be among the first 25 applicants Join to apply for the
Clinical Sub Investigator (PA / ARNP)
role at
K2 Medical Research Get AI-powered advice on this job and more exclusive features. Direct message the job poster from K2 Medical Research Strategy and Development | Marketing, HR, & Talent Management
Clinical Research Investigator
At K2 Medical Research, a privately-owned clinical research facility with multiple locations in Florida, Tennessee, and Rhode Island. We specialize in conducting multiphasic clinical trials that promote the development of innovative and effective medical treatments while maintaining the safety and privacy of our participants. Here at K2, we are committed to fighting the diseases that plague our loved ones and ourselves. By harnessing the power of advanced clinical research and connecting our patients with the treatments of tomorrow, we can improve the health of our local communities, and by extent, the population of our world.
We are seeking a
PA/ARNP/Sub Investigator for our Nashville clinic.
The Sub Investigator promotes Good Clinical Practice in the conduct of clinical investigations by ensuring adherence to protocol requirements, protecting the rights and welfare of study subjects, assuring the integrity of data generated at the site and directing the conduct of the clinical investigation according to federal and state regulations and guidance documents.
Primary Responsibilities
Provide investigator qualifications and agreements as required for study participation Maintain current, up-to-date curriculum vitae Maintain current licensure and continuing education Assume responsibility for the conduct of the clinical investigation Maintaining documentation of all aspects of the clinical investigation Ensure protocol compliance Ensure initial and ongoing review and oversight by a duly constituted IRB Provide adequate facilities to conduct the clinical trial Manage the medical care of study participants (subjects) Ensure validity of data reported to sponsor Ensure documentation of study-related procedures, processes, and events Ensure proper use, storage, and return or disposal of investigational agents Maintain professional and technical knowledge Reading, understanding and adhering to organizational Standard Operating Procedures Assisting in establishing and enforcing departmental standards Contributes to team effort by: Exploring new opportunities to add value to organization and departmental processes Helping others to achieve results Performing other duties as assigned Learns and maintains Technical and Industry Knowledge by Attending and participating in applicable company-sponsored training
Knowledge, Skills, And Abilities
Bachelor's degree in a health-related field Broad knowledge of general medicine and medical terminology Strong analytical and problem-solving skills Excellent organizational skills, detail oriented, efficient, and able to multi-task and prioritize effectively. Excellent interpersonal skills. BLS and/or ACLS Strong written and verbal communication skills. Bilingual skills preferred. Applicants that do not meet 100% of the above qualifications but who have a combination of related education and applicable experience may be considered upon approval
Qualifications
Licensed PA/ARNP/DNP in the state of TN
We value our employees and their professional and personal needs, and support these through our benefit offerings:
Benefits
Medical, Dental, Vision, Flexible Spending Accounts, Employer paid Long-Term disability and Life Insurance, Short Term Disability, Accident and Critical Illness Insurance, Voluntary Life and Long-Term Care Insurance, Legal Shield, Employee Assistance Program, and various discount programs. 401(K) Plans- Traditional and Roth plans are available; 4% employer match that is immediately vested PTO of 16 days per year, 17 days after the first year of FT employment 9 paid Holidays K2 observes a four-day work week, Monday through Thursday, for full time employees. Fridays are non-working days unless required by business needs.
Seniority level
Seniority level Entry level Employment type
Employment type Full-time Job function
Job function Research, Analyst, and Information Technology Industries Research Services Referrals increase your chances of interviewing at K2 Medical Research by 2x Get notified about new Clinical Investigator jobs in
Nashville, TN . Hematologist and Clinical Investigator - Tennessee Oncology
Clinical Research Coordinator 1 - VCC - VICTR
Clinical Research Coordinator I, Hematology/Oncology
Research Assistant 1 - Translational Oncology (Holowatyj Lab) (Coding Experience Preferred)
Clinical Research Coordinator / Project Manager
Advanced - Medical Science Liaison (MSL) Consultant Contract Opportunity
CRA 2 - Oncology, U.S. East Coast, Central or West Coast
Franklin, TN $69,800.00-$226,800.00 1 week ago Faculty, Pharmaceutical Sciences - Pharmacy and Pharmaceutical Sciences
Senior Medical Science Liaison - Lung Oncology - Tennessee, Kentucky, West Virginia
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We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr