パレクセルでの仕事
パレクセルは、臨床開発の上流から下流までのそれぞれの専門領域で、国内外の多くのお客様に高度なソリューションを提供するプロフェッショナル集団です。 パレクセルは、新しい薬や治療法を、それらを必要としている人々にいち早く届けることを目指し、日々の業務に取り組んでいます。
Clinical Research Staff - RN or Paramedic
応募 求人ID R0000031809 ロケーション アメリカ合衆国 仕事内容On site position in New Haven, CT***** Must have CT Licensure and ACLS
Responsibilities: Paramedic
• Owns, maintains, and ensures clinical training transcripts are up to date at all times.
• Maintains proficiency in various clinical procedures required in study execution.
• Ensures clinical research studies are conducted according to protocol requirements and
internal SOPs, guidelines, work instructions, and process maps.
• Provides basic first aid and medical/nursing care within scope of practice.
• Assists in sample management, collection, and generation of computer labels.
• Records adverse events with referral to medical or nursing personnel for evaluation &
treatment.
• Performs electronic and diagnostic measurements including audiograms,
electrocardiograms, visual exams, and other novel devices.
• Performs and records physical measurements including vital signs and body
measurements.
• Creates volunteer identification (photos, badges).
• Provides necessary instructions to research participants.
• Monitors and maintains usage of daily clinic supplies.
• Maintains equipment log & calibration records.
• Creates and ensures quality in work and data output by performing data cache review.
• Attends various clinical meetings (i.e. study start-up, in-service, department meetings,
etc.).
• Supports other additional clinical functions.
• Demonstrates holistic understanding of work processes at the Unit.
• Identifies with overall goals of the NHCRU and progresses clinical research studies as
planned.
• Assists in the overall planning and delivery of clinical trials.
• Assists in the delivery of improved training program.
• Leads/supervises clinic pCROs (and colleagues, as appropriate) during various shifts of
operation as required.
• Provides/ supervises clinic support activities such as scheduling (e.g., bed space,
volunteer, staffing), supply requisitions and training, as required.
• Collaborates with clinical coordinators and clinical floor leads to maximize study
implementation.
Qualifications
• Preferred Associate in Science degree in Life, Biomedical, or Social Science. Bachelor of
Science in a health-related field desirable.
• Preferred qualifications include minimum of 1-2 years of work experience in clinical
research trials as data collector or clinical coordinator.
• State of Connecticut licensure as EMT-P.
• Quality conscious with high degree of ethics and integrity carrying out duties in
accordance to laws, regulatory standards, and with company policies and procedures.
• Proficiency in Microsoft (MS) Office and the ability to learn different software programs.
• Current certification in Basic Life Support (BLS) and Advanced Cardiovascular Life
Support (ACLS) required.
• Ability to work beyond normal work hours and various shift availability required.
RN
Primary Duties: RN
- Owns, maintains, and ensures clinical training transcripts are up to date at all times.
- Maintains proficiency in various clinical procedures required in study execution.
- Ensures clinical research studies are conducted according to protocol requirements and internal SOPs, guidelines, work instructions, and process maps.
- Provides basic first aid and medical/nursing care within scope of practice.
- Assists in sample management, collection, and generation of computer labels.
- Records adverse events with referral to medical or nursing personnel for evaluation & treatment.
- Performs electronic and diagnostic measurements including audiograms, electrocardiograms, visual exams, and other novel devices.
- Performs and records physical measurements including vital signs and body measurements.
- Creates volunteer identification (photos, badges).
- Provides necessary instructions to research participants.
- Monitors and maintains usage of daily clinic supplies.
- Maintains equipment log & calibration records.
- Creates and ensures quality in work and data output by performing data cache review.
- Attends various clinical meetings (i.e. study start-up, in-service, department meetings, etc.).
- Supports other additional clinical functions as delegated by the Client.
- Demonstrates holistic understanding of work processes at the Unit.
- Identifies with overall goals of the Client’s CRU and progresses clinical research studies as planned.
- Assists in the overall planning and delivery of clinical trials.
- Assists in the delivery of improved training program.
- Leads/supervises clinic contractors (and colleagues, as appropriate) during various shifts of operation as required.
- Provides/ supervises clinic support activities such as scheduling (e.g., bed space, volunteer, staffing), supply requisitions and training, as required.
- Collaborates with clinical coordinators and clinical floor leads to maximize study implementation.
- Completes training assigned by Client and/or PXL, as necessary, including general training requirements, SOPs, system, and process related training.
- Adheres to PXL and Client SOPs and processes.
Skills and Education:
- Minimum of an Associate in Science degree in Life, Biomedical, or Social science. Bachelor of Science in a health-related field desirable.
- Minimum of 1-2 years of work experience in clinical research trials as data collector, clinical coordinator, or clinical research nurse is preferred.
- State of Connecticut licensure as RN.
- Quality conscious with high degree of ethics and integrity carrying out duties in accordance to laws, regulatory standards, and with company policies and procedures.
- Proficiency in Microsoft (MS) Office and the ability to learn different software programs.
- Current certification in Basic Life Support (BLS) and Advanced Cardiovascular Life Support (ACLS) required.
- Ability to work beyond normal work hours and various shift availability required.
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