Clinical Trial Manager - Pharmaceutical

Placements24

United States

Remote

USD 90,000 - 130,000

Full time

4 days ago
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Benefits offered by this job

Annual incentives
Health, dental, vision
Vehicle or travel allowance
Professional growth
Collaborative environment

Job summary

Placements24 is seeking a highly organized Clinical Trial Manager to oversee research initiatives within their pharmaceutical division in George. You will plan, execute, and monitor clinical trials, ensuring regulatory compliance and alignment with company policies.

The role requires deep knowledge of trial methodology, strong leadership, and the ability to coordinate sites, CROs, and other vendors across multiple studies from Phase I to IV.

Qualifications

  • Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
  • 7+ years of clinical trial management experience.
  • Deep knowledge of FDA/EMA/ICH-GCP regulations.
  • Experience managing multiple trials from Phase I to IV.
  • Strong leadership and communication skills.
  • Ability to coordinate across sites and functions.

Responsibilities

  • Develop and manage trial protocols, plans, and budgets per ICH-GCP.
  • Oversee site selection, initiation, monitoring, and close-out.
  • Ensure timely patient enrollment and protocol adherence.
  • Manage relationships with sites, CROs, and external vendors.
  • Monitor progress, identify risks, and implement corrective actions.
  • Maintain trial documentation and regulatory compliance.

Skills

Leadership
Project management
Regulatory knowledge
ICH-GCP expertise
Cross-functional collaboration
Problem-solving

Education

Bachelor's degree in Life Sciences/related
Master's degree preferred

Job description

About the Role

Our client is seeking a highly organized and experienced Clinical Trial Manager to oversee critical research initiatives within their pharmaceutical division in George . You will be responsible for the planning, execution, and monitoring of clinical trials, ensuring compliance with regulatory standards and company policies. This role requires a proactive individual with a deep understanding of clinical research methodologies and a passion for bringing new treatments to patients. Join a forward-thinking organization dedicated to advancing healthcare through rigorous scientific investigation and a commitment to ethical research practices.

Key Responsibilities
  • Develop and manage comprehensive clinical trial protocols, project plans, and budgets in accordance with ICH-GCP guidelines.
  • Oversee all aspects of clinical trial conduct, including site selection, initiation, monitoring, and close-out activities.
  • Ensure the timely enrollment of patients and adherence to protocol requirements at all participating clinical sites.
  • Manage relationships with investigational sites , contract research organizations (CROs), and other external vendors.
  • Monitor study progress, identify potential risks and issues, and implement corrective actions as needed.
  • Maintain accurate and complete trial documentation, ensuring data integrity and regulatory compliance for studies conducted in George .
Requirements
  • Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field; Master's degree preferred.
  • Minimum of 7 years of experience in clinical trial management within the pharmaceutical or biotechnology industry.
  • In-depth knowledge of clinical trial regulations (e.g., FDA, EMA, ICH-GCP).
  • Demonstrated experience in managing multiple clinical trials simultaneously, from Phase I to Phase IV.
  • Strong leadership, negotiation, and problem-solving skills.
  • Excellent communication and organizational abilities, essential for coordinating efforts across various teams and locations.
Benefits
  • Competitive salary package with annual performance incentives.
  • Comprehensive health, dental, and vision insurance.
  • Company-provided vehicle or travel allowance.
  • Opportunities for professional growth and advanced training in clinical research.
  • A collaborative and supportive work environment focused on patient outcomes and scientific advancement.
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