Paramedic providing emergency and advanced medical care to study participants within a Fortrea Clinical Research Unit, ensuring safety and compliance with study protocols.
Responsibilities
Collaborate with physicians, nurses, and medical team members to support coordinated participant care
Deliver basic and advanced medical care in emergent and non-emergent situations
Lead resuscitation and stabilization efforts for life‑threatening situations
Monitor, document, and review active adverse events
Administer medications and treatments per investigator or physician orders
Coordinate clinical research studies in accordance with study protocols, Good Clinical Practice (GCP), FDA regulations, and applicable standard operating procedures.
Compensation
$70,000 to $80,000 annually, depending on experience, education, certifications, and qualifications
Responsibilities
Coordinate clinical research studies in accordance with study protocols, Good Clinical Practice (GCP), FDA regulations, and applicable standard operating procedures.
Manage study activities, including participant screening, enrollment, scheduling, study visits, and follow-up.
Facilitate and document the informed consent process in accordance with applicable regulations and study requirements.
Coordinate and perform protocol-required study procedures within the scope of training and qualifications.
Maintain accurate and timely source documentation, electronic data capture (EDC) entries, and data query resolution.
Requirements
Associate's or bachelor's degree in a healthcare, life sciences, or related field
Nice to have: Experience coordinating pharmaceutical-sponsored or industry-initiated clinical trials
Nice to have: ACRP or SOCRA certification (CCRC or CCRP)
Nice to have: Medical Assistant, Phlebotomy, or other relevant clinical certification
Nice to have: Experience performing venipuncture, processing laboratory specimens, or managing investigational products
Responsible for design, execution, oversight, and monitoring of internal and external clinical studies supporting product development and evidence generation for Lingo.
Compensation
The base pay for this position is $114,000.00 – $228,000.00
Responsibilities
Design, execute, monitor, and analyze internal and external clinical studies
Provide scientific leadership and subject matter expertise in metabolic health
Collaborate with Medical Affairs, Marketing, Product Development, Regulatory Affairs, and other cross-functional stakeholders
Develop, implement, and maintain clinical research operating procedures
Participate in cross-functional product development and commercialization teams
The Manager Clinical Research Monitoring leads the development and implementation of a centralized, risk-based post-approval monitoring program for OSF HealthCare’s research enterprise.
Compensation
Expected pay for this position is $42.64 - $56.50/hour. Actual pay will be determined by experience, skills and internal equity. This is a Salaried position.
Responsibilities
Oversee monitoring and audit activities across active research studies
Ensure compliance with federal regulations, Good Clinical Practice (GCP), institutional policies, and approved study protocols
Partner with Research Administration leadership, investigators, and research teams to identify compliance risks
Strengthen research quality and support safe and effective conduct of clinical research
Requirements
Bachelor’s degree in healthcare, life sciences, nursing, public health, regulatory science, or related field
Support in‑life study activities for rodent and non‑rodent safety/toxicology studies, ensuring compliance with protocols, SOPs, GLP, and animal welfare standards.
Compensation
The salary for this position ranges from $26.86 to $44.77 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company’s policies.
Responsibilities
Perform assigned in vivo study activities in compliance with regulatory requirements
Support the in‑life phase of rodent and non‑rodent safety/toxicology studies
Read, understand, and follow study protocols
Accurately enter, review, and document study data
Perform self‑review and peer review of in‑life data
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Clinical Research CoordinatorHeadlands Research · Stockbridge, US