Clinical Research Coordinator II - Impactful Trials & Compliance

Planet Pharma; Lufkin (TX); On-site; USD 41,000 - 44,000; Full time

Job summary

Planet Pharma in the United States is seeking a Clinical Research Coordinator (CRC) to support an ongoing study with data entry, query resolution, and other CRC activities. The ideal candidate will have CRC experience and strong collaboration skills, with a diplomatic, agile, and adaptable approach in interactions with stakeholders.

The role emphasizes adherence to GCP/ICH, IRB processes, and accurate data handling, including patient bookings and sponsor system entries.

Qualifications

• Bachelor’s degree or equivalent and relevant formal academic qualification in the clinical/medical field.
• 2+ years’ experience in a CRC role or similar clinical research position.
• Solid understanding of GCP, SOPs, informed consent and safety monitoring.

Responsibilities

• Conduct clinical studies according to FDA/GCP and ICH regulations and guidelines.
• Record patient information and test results on required forms.
• Complete IP accountability logs and related information as needed.
• Report suspected non-compliance to site staff.
• Ensure IRB approval and compliance throughout the study.
• Promote the company and build positive patient relationships to support retention.
• Attend site initiation and related trainings to learn protocol.
• Call patients, schedule bookings, and perform follow-up communications as needed.
• Log data in sponsor systems and ensure accuracy and timeliness.
• Gathers and maintains source documents and up-to-date patient files.
• Adhere to COP/SCOP; assist with waste disposal and site neatness.

Skills

Clinical research knowledge

Communication skills

Attention to detail

Problem solving

Team collaboration

English fluency

Education

Bachelor’s degree or equivalent in clinical/medical field

Job description

Planet Pharma in the United States is seeking a Clinical Research Coordinator (CRC) to support an ongoing study with data entry, query resolution, and other CRC activities. The ideal candidate will have CRC experience and strong collaboration skills, with a diplomatic, agile, and adaptable approach in interactions with stakeholders.

The role emphasizes adherence to GCP/ICH, IRB processes, and accurate data handling, including patient bookings and sponsor system entries.