#994 - Clinical Trial Manager (CTM)

Responsibilities

• Lead and oversee the day-to-day operational execution of assigned clinical trials.
• Develop and maintain study timelines, milestones, and operational plans.
• Cook up and manage relationships with CROs, vendors, clinical sites, and other external partners.
• Maintain study progress, identify risks, issues, and potential delays, and implement appropriate mitigation strategies.
• Ensure clinical trial activities comply with the protocol, ICH-GCP, applicable regulations, and company SOPs.
• Collaborate with Clinical Operations, Regulatory, Medical, Data Management, Pharmacovigilance, Biostatistics, and other cross-functional teams.
• Review and follow up on study metrics, KPIs, quality indicators, and key operational deliverables.
• Contribute to study budgets, vendor management, and financial tracking.
• Prepare and participate in study team meetings and presentations for internal and external stakeholders.
• Communicate study status, risks, and key decisions effectively to US-based client stakeholders.

Requirements

• Advanced English proficiency (C1 or equivalent), both written and spoken, with the ability to confidently participate in meetings and communicate with US-based stakeholders.
• 3+ years of experience in clinical research, with relevant experience in Clinical Trial Management or Clinical Operations.
• Experience managing clinical trials within a pharmaceutical, biotechnology, CRO, or related healthcare organization.
• Solid knowledge of ICH-GCP, clinical research processes, and applicable regulatory requirements.
• Experience coordinating CROs, vendors, clinical sites, and cross-functional teams.
• Strong project management, organizational, and problem-solving skills.
• Ability to manage multiple priorities and deliver against timelines in a remote, international environment.
• Excellent communication and interpersonal skills.
• Strong proficiency with Microsoft Office and common clinical trial/project management systems.

Qualifications

• Bachelor's degree in Life Sciences, Pharmacy, Nursing, Medicine, or a related field.
• Preferred qualifications include:
• Experience working on global or multinational clinical trials.
• Previous experience working directly with US-based pharmaceutical clients or stakeholders.
• Experience in Phase I–III clinical development.
• Experience with electronic clinical trial systems and clinical trial management platforms.
• PMP, ACRP, SOCRA, or other relevant clinical research/project management certification.

Benefits

Salary in USD.

100% Remote work.

Duration: Long-term.

Type of contract: Independent Contractor with Venon Solutions LLC.

Paid Time Off: 2 weeks / 10 business days.

Paid Holidays from the US calendar.

Working hours: Full-time EST, fully committed.