Offer summary

Qualifications:

Licensed physician in good standing with board certification in cardiology., 1-2 years of experience in pharmaceutical clinical research or related fields is preferred., Excellent verbal and written communication skills for effective collaboration., Strong computer skills and proficiency in Microsoft Office and relevant software..

Key responsabilities:

Perform ECG and Holter review and analysis according to established protocols.

Consult with the Principal Investigator on participant safety in clinical trials.

Provide expert consultation on cardiovascular matters and address team inquiries.

Participate in core laboratory meetings and contribute to process improvement initiatives.

Job description

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.

Job Purpose

The Cardiologist will perform ECG and Holter review and analysis in strict adherence with established protocols and procedures. They will also serve as a consultant to the Principal Investigator team to monitor the safety of participants enrolled in clinical trials. Additionally, they will act as an educational resource and consultant on cardiovascular matters.

Essential Functions

Adjudication of Cardiodynamic ECGs: Conduct timely and blinded interpretation and measurement of cardiodynamic ECGs consistent with the accuracy and precision required at Celerion for regulatory submission.

Safety ECG Review: Provide consultative services involving the review of safety ECGs in collaboration with the Principal Investigator (PI) or their designee to aid in subject management decisions.

Holter Review: Analyze continuous digital Holter recordings for potential dysrhythmias that would impact subject safety.

Consultation Availability: Provide expert consultation on cardiovascular, clinical, or core laboratory specific findings, addressing questions from team members that require specialized cardiology insights and recommendations.

Adverse Event Notification: Promptly alert the Principal Investigator (PI) or their designee to any potentially serious adverse clinical events identified during the review of cardiovascular data.

Core Laboratory Meetings: Actively participate in monthly core laboratory staff meetings to discuss salient issues, provide educational insights, and offer feedback to enhance team collaboration and performance.

Compliance Adherence: Ensure strict compliance with all procedure guidelines (WIs), standard operating procedures (SOPs), and training requirements.

Continuing Education and Licensing: Maintain all continuing education and licensing requirements as mandated by the state in which they are licensed to practice medicine.

Quality Assessment Participation: Engage in annual quality assessment exercises to ensure maintenance of clinical competence in ECG reading skills and evaluate intra-reader and inter-reader variability.

Process Improvement Contributions: Provide valuable input and recommendations into core laboratory processes and procedures designed to enhance accuracy, precision, and operational efficiency.

These functions are integral to support patient safety, preserve data integrity and uphold the outstanding reputation enjoyed by Celerion as an industry leader in early phase clinical trials.

Knowledge/Skills/Education/Licenses

Educational Background: Licensed physician in good standing with board certification or equivalent in cardiology

Experience: (Preferred) 1-2 years of experience in pharmaceutical clinical research, the biotech industry, or as a member of a Contract Research Organization (CRO).

Communication Skills: Excellent verbal and written communication skills to facilitate effective collaboration with colleagues, departments, and clients.

Technology Proficiency: Demonstrate strong computer skills with the ability to troubleshoot general issues. Proficient in Microsoft Word, Excel, PowerPoint, Outlook, Veeva, and department-specific software, ensuring seamless integration of technology into daily operations.

Independence and Organizational Skills: Display a high level of organization and the ability to work independently effectively managing multiple priorities.

Problem-Solving: Exhibit solid problem-solving and decision-making skills, navigating complex challenges with confidence and efficiency.

Innovation: Exhibit an inquisitive demeanor and a desire to develop innovative approaches pertaining to core laboratory efficiency and cardiovascular service offerings

Passion for Science: Strong commitment to learning and advancing scientific knowledge within the field of new drug development and regulatory guidance.

Continuing Education: Maintain and enhance subject matter expertise by engaging in ongoing education programs and webinars related to early phase pharmaceutical research.

Availability for occasional on-site, telephone, or email consultations is required.

Celerion Values: Integrity Trust Teamwork Respect

Are you ready to join our team?

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.

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