Pinnacle Clinical Research

Clinical Research Data Coordinator

AUSTIN, TXPosted 30+ days ago

Job summary

  • Job post source

    This job is directly from Pinnacle Clinical Research

  • Job overview

    The Clinical Research Data Coordinator at Pinnacle Clinical Research is responsible for abstracting and entering clinical and research data to support multiple clinical trials, ensuring data quality and regulatory compliance to advance medical discovery.

  • Responsibilities and impact

    The role involves abstracting data from medical records, managing data in clinical trial systems, resolving queries, auditing data entries, preparing for audits, collaborating with internal and external stakeholders, and supporting quality assurance processes.

  • Compensation and benefits

    The position offers competitive pay commensurate with experience, 401k, medical, dental, vision insurance, paid time off including 3 weeks PTO and 14 holidays, and additional perks like a tranquility room, gym access, and scrub vouchers at specific locations.

  • Experience and skills

    Candidates should have a Bachelor's degree or equivalent experience, 1-2 years of clinical research data entry experience, knowledge of clinical research regulations (CFR, GCP, HIPAA), proficiency in Microsoft Office, familiarity with clinical trial management software, basic medical knowledge, and strong communication and organizational skills.

  • Career development

    Pinnacle Clinical Research provides opportunities for personal and professional growth in a team-oriented environment within the healthcare industry.

  • Work environment and culture

    The company values integrity, professionalism, and a team-oriented work environment, promoting high standards and ethical conduct with supportive amenities like tranquility rooms and gyms at certain locations.

  • Company information

    Pinnacle Clinical Research is dedicated to advancing medical knowledge through rigorous clinical research studies that complement routine patient care and aim to transform healthcare.

  • Team overview

    The Clinical Research Data Coordinator reports to the Director of Compliance and Data Management and works collaboratively with internal site staff and external stakeholders including physicians, nurses, and sponsor representatives.

  • Unique job features

    The role offers unique opportunities to work on multiple complex clinical trials with direct impact on medical research quality and compliance, supported by specialized tools like Clinical Research IO and involvement in regulatory audit preparations.

Company overview

Pinnacle Clinical Research is a leading clinical trial organization specializing in gastroenterology and hepatology. They conduct advanced clinical trials to develop new treatments for liver diseases, including non-alcoholic steatohepatitis (NASH) and cirrhosis. The company generates revenue through partnerships with pharmaceutical companies and research grants. Founded by Dr. Stephen Harrison, a renowned hepatologist, Pinnacle has a strong reputation for its cutting-edge research and contributions to medical advancements in liver health.

How to land this job

  • Tailor your resume to highlight your experience with clinical data abstraction, data entry, and familiarity with electronic data capture systems like CTMS and EDC, emphasizing accuracy and regulatory compliance.

  • Showcase your knowledge of clinical research regulations such as FDA, GCP, HIPAA, and your ability to maintain confidentiality and data integrity under these standards.

  • Apply through multiple platforms including Pinnacle Clinical Research’s corporate careers page, LinkedIn job postings, and relevant clinical research job boards to maximize exposure.

  • Connect with current employees in Pinnacle Clinical Research’s Compliance and Data Management division on LinkedIn; start conversations by referencing recent clinical trial innovations at Pinnacle or asking about best practices for data quality assurance at Pinnacle Clinical Research.

  • Optimize your resume for ATS by incorporating keywords from the job description such as 'clinical data abstraction,' 'CTMS (CRIO),' 'data management,' 'regulatory compliance,' and 'Good Clinical Practices' to improve screening success.

  • Leverage Jennie Johnson’s Power Apply feature to automate tailored applications across multiple channels and identify LinkedIn contacts for networking, allowing you to focus your efforts on preparing for interviews and refining your professional profile.

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