Clinical Safety Officer

Actalent; Kansas; On-site; USD 41,000 - 45,000; Part time

Benefits offered by this job

Medical, dental & vision

Critical Illness, Accident, Hospital

401(k) Retirement Plan

Life Insurance

Short and long-term disability

Health Spending Account (HSA)

Transportation benefits

Job summary

Actalent is seeking a PRN Paramedic to join a clinical safety team in Overland Park, KS. This contract position requires availability for at least 4 shifts per month, each 4+ hours, supporting safety monitoring during study conduct.

Responsibilities include safety oversight, adherence to GCP/SOPs, AE documentation, and IP administration as needed. ACLS/BLS certification preferred; training provided if not held.

Qualifications

• Availability for at least 4 shifts per month, with each shift 4+ hours.
• Pre-screening patients, recruitment, safety assessments, chart review, and clinical research skills.

Responsibilities

• Oversee the safety of clinical trial participants and maintain safety equipment.
• Execute tasks in compliance with study protocol, GCP, and SOPs.
• Ensure confidentiality of participants and sponsors.
• Monitor, document, and follow-up on adverse events.
• Continuously assess safety improvements and report findings to management.
• Conduct trial activities including monitoring, safety assessments, IP administration, and catheter installation.

Skills

4+ shifts per month

Pre-screening & recruitment

Tools

ACLS/BLS certification

Job description

Job Description

Job Description

Job Title: Clinical Safety Officer - Paramedic

Job Description

We are seeking a PRN Paramedic in Overland Park, KS to join our team and ensure the safety of clinical trial participants during study conduct. This position is part of a Variable Hour Employee staffing program, designed to supplement our staffing needs based on fluctuating business requirements.

Responsibilities

• Oversee the safety of clinical trial participants and maintain safety equipment.
• Execute tasks in compliance with study protocol, Good Clinical Practices (GCP), and Standard Operating Procedures (SOPs).
• Ensure the confidentiality of clinical trial participants and sponsors.
• Monitor, document, and follow-up on participant adverse events.
• Continuously assess safety improvement opportunities and communicate findings to departmental management.
• Perform clinical trial activities including continuous monitoring, safety assessments, Investigational Product (IP) administration, and catheter installation.

Essential Skills

• Ability to provide availability for at least 4 shifts per month, with each shift being at least 4 hours in length.
• Pre-screening patients, patient recruitment, safety assessments, chart review, and clinical research skills.

Additional Skills & Qualifications

• No clinical research experience needed.
• ACLS or BLS certification preferred, but training will be provided if not already obtained.

Work Environment

This position operates in a clinical research unit located in a suburb of Kansas. The role will require flexible scheduling based on business needs and availability, without guaranteed hours. Employees are expected to follow proper call-off procedures in case of unavailability due to vacations, illness, or family emergencies.

Job Type & Location

This is a Contract position based out of Overland Park, KS.

Pay and Benefits

The pay range for this position is $30.00 - $33.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits