Senior Clinical Trial Manager

eteraflex connects; United States; Remote; USD 90,000 - 160,000; Part time

Job summary

A leading company is seeking a part-time Clinical Trial Manager (CTM) for contract engagement to establish SOPs and documentation frameworks in clinical operations. Ideal for experienced professionals, this role offers flexibility and the chance to influence early-stage clinical processes.

Qualifications

• Minimum 5–7 years of experience as a CTM or similar role in clinical research.
• Strong background in SOP development and trial startup.
• Familiarity with U.S. and global regulatory requirements.

Responsibilities

• Lead the development and documentation of SOPs for clinical trial conduct.
• Collaborate with internal teams to align procedures.
• Support coordination activities with existing CTMs and external partners.

Skills

SOP development

Trial startup

Regulatory compliance

Communication skills

Organizational skills

Job description

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Contract Clinical Trial Manager (Part-Time)

Location: Remote / U.S.-based preferred

Type: Contract | Part-Time

About the Role:

We are seeking an experienced Clinical Trial Manager (CTM) on a contract and part-time basis (Time and Material) to assist with the establishment of Standard Operating Procedures (SOPs), documentation frameworks, and cross-functional coordination for early-stage clinical operations. This role is ideal for someone who can provide strategic input and operational support in a flexible on-demand engagement model.

Key Responsibilities:

• Lead the development and documentation of SOPs, process flows, and best practices for clinical trial conduct.
• Collaborate with internal teams (e.g., regulatory, clinical, quality) to align procedures and responsibilities.
• Support coordination activities with existing CTMs, CRAs, and external partners as needed.
• Provide guidance on regulatory and GCP-compliant operational processes.
• Assist in building scalable templates, trackers, and project documentation systems.
• Offer on-demand expertise for startup planning and vendor communication.
• Experience with India regulatory submission processes (e.g., CT-04, CT-16, CDSCO, SEC) is a strong plus.

Qualifications:

• Minimum 5–7 years of experience as a CTM or similar role in clinical research.
• Strong background in SOP development and trial startup, sites operations.
• Familiarity with U.S. and global regulatory requirements (FDA, ICH GCP).
• Experience with India-specific regulatory filings and clinical trial submissions is highly desirable.
• Excellent organizational and communication skills.
• Comfortable with ambiguity and capable of working independently in a lean environment.
• Part-time
• Ideal for experienced professionals seeking flexible consulting work.
• Duration: Initial 3–6 months, with potential for extension based on need.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Part-time

Job function

• Job function

  Health Care Provider, Science, and Research

• Industries

  Biotechnology Research, Research Services, and Hospitals and Health Care

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