Clinical Admin Ops

A-Line Staffing Solutions; Cary (NC); Híbrido; USD 42 000 - 62 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Benefits after 90 days

Resumo da oferta

A-Line Staffing Solutions LLC in Cary, NC seeks a Clinical Admin Ops to create and submit adverse event and product complaint reports from patient management system data. You will perform quality checks on drug information, manufacturer details, spelling and grammar, and communicate with clinicians on questions about reporting.

The role requires strong written and verbal communication, organization, time management, and data entry accuracy.

Qualificações

• Bachelor's degree or equivalent experience preferred.
• Pharmacovigilance experience preferred.
• Pharmacy technician or other clinical background preferred.
• Oncology experience is a plus.

Responsabilidades

• Create and submit adverse event and product complaint reports from patient management system data.
• Perform quality checks for accuracy, spelling, drug information, manufacturer details, and grammar.
• Communicate with clinicians regarding questions or concerns related to adverse event reporting.
• Identify missing adverse events and product complaints through daily quality checks.
• Ensure identified missing reports are submitted and properly accounted for.
• Prepare and submit reconciliation reports to biopharmaceutical stakeholders.
• Assist clinical auditors in identifying trends and issues in adverse event reporting.

Conhecimentos

Communication

Organization

Time management

Computer skills

Spreadsheet proficiency

Multitasking

Interpersonal skills

Attention to detail

Data entry

Numerical data entry

Formação académica

Bachelor's degree

Descrição da oferta de emprego

Job Title:2 Clinical Admin Ops

Address: Cary, NC

Create and submit adverse event and product complaint reports from patient management system data. Perform quality checks for accuracy, spelling, drug information, manufacturer details, and grammar. Communicate with clinicians regarding questions or concerns related to adverse event reporting. Identify missing adverse events and product complaints through daily quality checks. Ensure identified missing reports are submitted and properly accounted for. Prepare and submit reconciliation reports to biopharmaceutical stakeholders. Assist clinical auditors in identifying trends and issues in adverse event reporting.

Critical Information

Work schedule: 9:00 a.m.–6:00 p.m. Eastern or 10:00 a.m.–7:00 p.m. Eastern.

Hybrid onboarding and training at the Cary, NC location, followed by remote work.

Candidate must be local to Cary, NC, within a 60-mile radius.

Strong written and verbal communication, organization, time management, computer, spreadsheet, multitasking, interpersonal, adaptability, and attention-to-detail skills are required.

Rapid and accurate numerical and text data entry is essential.

Pharmacovigilance experience is strongly preferred.

Education/Licenses Needed Bachelor's degree or equivalent experience preferred.

Pharmacy technician or other clinical background preferred.

Prior pharmacy experience preferred.

Oncology experience is a plus.

Benefits:

• Benefits are available to full-time employees after 90 days of employment.

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