Clinical Research Lead - Protocol Design & Trials

Planet Pharma; Saint Paul (MN); On-site; USD 90,000 - 130,000; Full time

Job summary

Planet Pharma is seeking a Clinical Research Specialist in the United States to oversee and design clinical evaluation studies in alignment with SOPs and regulatory standards.

The role includes preparing protocols, authoring patient forms, conducting studies, and interpreting results for potential medical or commercial products. Collaboration with project teams and vendors is required.

Qualifications

• Practical knowledge in clinical research with demonstrated competence.
• Must meet regulatory requirements and SOP/GCP standards.
• Minimum 2 years of relevant experience in clinical research.

Responsibilities

• Oversees, designs, plans and develops clinical evaluation research studies.
• Prepares and authors protocols and patient record forms.
• Conducts registered and non-registered clinical studies of products with potential medical or commercial value.
• Oversees and interprets results of clinical investigations for new drug, device, or consumer applications.
• Manages operational aspects of trials with project teams, SOPs, and country regulations; may prepare budgets.
• May handle clinical supply operations, site and vendor selection.
• Represents the company regionally in clinical research discussions and collects feedback from stakeholders.
• Builds relationships with internal and external parties and drives local evidence dissemination.

Skills

Clinical research

Regulatory compliance

SOP adherence

GCP knowledge

Project coordination

Education

Bachelor's degree

2 years relevant experience

Job description

Planet Pharma is seeking a Clinical Research Specialist in the United States to oversee and design clinical evaluation studies in alignment with SOPs and regulatory standards.

The role includes preparing protocols, authoring patient forms, conducting studies, and interpreting results for potential medical or commercial products. Collaboration with project teams and vendors is required.