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Float Clinical Research Coordinator Ii

Fresenius Medical Care
2-5 years
$70,000 – $100,000
Remote
1 June 22, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Float Clinical Research Coordinator II

Location: Remote (USA – Extensive Travel Required)
Company: Fresenius Medical Care
Department: Clinical Research Operations
Employment Type: Full-Time

Role Summary

The Float Clinical Research Coordinator II is responsible for coordinating and managing clinical research studies across multiple sites while ensuring compliance with study protocols, GCP, ICH, FDA regulations, and company SOPs. The role oversees patient recruitment, informed consent, study conduct, data collection, regulatory documentation, safety monitoring, and site coordination activities.

This position serves as the primary liaison between Sponsors, CROs, Investigators, clinical staff, and study participants while ensuring subject safety, protocol compliance, data integrity, and successful study execution. The role requires extensive travel (up to 80%) across multiple research locations.

Key Responsibilities

Clinical Trial Coordination

  • Coordinate clinical studies from study start-up through close-out.

  • Manage multiple concurrent studies across various sites.

  • Ensure protocol compliance throughout the study lifecycle.

  • Coordinate all study-related activities according to timelines and study requirements.

  • Monitor study progress and resolve operational challenges.

Patient Recruitment & Enrollment

  • Support patient identification and pre-screening activities.

  • Coordinate participant enrollment according to inclusion/exclusion criteria.

  • Ensure study enrollment targets are achieved.

  • Educate potential participants regarding study requirements.

  • Maintain participant retention throughout study duration.

Informed Consent & Subject Management

  • Conduct informed consent process in accordance with GCP guidelines.

  • Educate study participants regarding:

    • Study Procedures

    • Risks & Benefits

    • Safety Requirements

    • Privacy & Confidentiality

    • Rights & Responsibilities

  • Protect participant rights, safety, and wellbeing.

  • Monitor participant progress throughout study participation.

Clinical Data Management

  • Collect, verify, and maintain accurate clinical research data.

  • Complete:

    • Electronic Case Report Forms (eCRFs)

    • Paper CRFs

    • Clinical Trial Management Systems (CTMS)

  • Ensure data accuracy, completeness, and timeliness.

  • Maintain source documentation according to regulatory requirements.

Safety Monitoring & Adverse Event Management

  • Monitor subject safety throughout study participation.

  • Identify and report:

    • Adverse Events (AEs)

    • Serious Adverse Events (SAEs)

    • Safety Concerns

  • Escalate safety issues to Principal Investigator (PI).

  • Ensure appropriate documentation and reporting of safety events.

Regulatory & Compliance Management

  • Ensure compliance with:

    • ICH-GCP Guidelines

    • FDA Regulations

    • HIPAA Requirements

    • IRB Requirements

    • Sponsor Requirements

  • Prepare and maintain regulatory documentation.

  • Support audits, inspections, and monitoring visits.

  • Maintain study files in audit-ready condition.

Site & Study Management

  • Serve as primary point of contact between:

    • Sponsors

    • CROs

    • Principal Investigators

    • Clinical Teams

  • Coordinate study logistics across multiple sites.

  • Ensure study supplies, investigational products, and equipment are properly managed.

  • Support site initiation, monitoring, and close-out activities.

Clinical Operations Support

  • Manage study-specific budgets and resources.

  • Support contract and budget discussions.

  • Track participant reimbursement and study payments.

  • Ensure research activities are appropriately documented and billed.

Training & Staff Development

  • Assist in onboarding and training research personnel.

  • Educate clinical staff on study-specific procedures.

  • Maintain required certifications and mandatory training.

  • Support protocol-specific competency development.

Documentation & Reporting

  • Maintain:

    • Regulatory Binders

    • Study Files

    • Subject Records

    • Enrollment Logs

    • Training Records

  • Generate study reports and progress updates.

  • Ensure proper documentation throughout study lifecycle.

Required Qualifications

Education

  • Associate Degree (AA) in Life Sciences, Healthcare, or related field (Preferred)

  • Graduate of a Healthcare Technical Program (Preferred)

Preferred Degrees

  • B.Sc Life Sciences

  • M.Sc Life Sciences

  • B.Pharm

  • M.Pharm

  • B.Sc Nursing

  • M.Sc Nursing

  • BPT

  • MPT

  • BHMS

  • BAMS

  • MBBS

  • Clinical Research Degrees

Experience

  • 2–5+ years of Clinical Research Coordination experience.

  • Experience managing:

    • Clinical Trials

    • Patient Recruitment

    • Regulatory Documentation

    • Site Management

    • Data Collection

  • Experience working with Sponsors, CROs, and Investigators preferred.