Are you a highly organized and experienced clinical professional with a passion for improving patients' lives? Look no further! Catalent is seeking a dedicated Clinical Coordinator to join our team and play a crucial role in the development and execution of clinical trials. As a Clinical Coordinator, you will have the opportunity to work closely with cross-functional teams and external partners to ensure the success of our clinical programs. If you have a strong background in clinical operations, exceptional project management skills, and a desire to make a meaningful impact in the healthcare industry, we want to hear from you! Join us at Catalent and be a part of our mission to deliver innovative and life-changing therapies to patients in need.
- Plan and coordinate all aspects of clinical trials, including study design, timelines, and budgets.
- Collaborate with cross-functional teams to ensure alignment and execution of clinical trial protocols.
- Liaise with external partners, such as CROs, investigators, and study sites, to ensure smooth operation of clinical trials.
- Oversee patient recruitment and enrollment, ensuring all necessary ethical and regulatory approvals are obtained.
- Monitor and analyze data from clinical trials, identifying any issues or discrepancies and implementing corrective actions.
- Maintain accurate and up-to-date documentation of all clinical trial activities and ensure compliance with regulatory requirements.
- Develop and maintain relationships with key stakeholders, including healthcare professionals, patients, and study sponsors.
- Provide regular updates and reports on the progress of clinical trials to management and other relevant parties.
- Proactively identify potential risks and issues in clinical trial execution and develop contingency plans to mitigate them.
- Continuously evaluate and improve clinical trial processes and procedures to increase efficiency and effectiveness.
- Mentor and train junior clinical staff, ensuring their adherence to company policies and procedures.
- Stay current on industry trends, regulations, and guidelines related to clinical trials, and apply this knowledge to trial design and execution.
- Act as a representative of the company at industry conferences and events, showcasing our commitment to improving patients' lives through clinical research.
Bachelor's Degree In A Relevant Field Such As Healthcare Administration, Nursing, Or Clinical Research.
At Least 3-5 Years Of Experience In Clinical Research Coordination, Preferably In A Pharmaceutical Or Biotech Company.
Strong Knowledge Of Fda Regulations And Guidelines For Conducting Clinical Trials.
Excellent Organizational And Time-Management Skills, With The Ability To Handle Multiple Projects And Priorities Simultaneously.
Demonstrated Leadership Skills, Including The Ability To Effectively Manage A Team And Communicate With Cross-Functional Stakeholders.
Quality Assurance
Project Management
Data Analysis
Communication
Time Management
Budget management
Team Leadership
Risk assessment
Regulatory compliance
Organization
Problem-Solving
Clinical Trials
Communication
Conflict Resolution
Leadership
Time management
Interpersonal Skills
creativity
Critical thinking
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Clinical Coordinator in Philadelphia, PA, USA is between $56,000 and $79,000 per year. This range may vary depending on factors such as education, experience, and location. Clinical Coordinators in Philadelphia may also receive benefits such as health insurance, retirement plans, and paid time off.
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Catalent, Inc. is a multinational corporation headquartered in Somerset, New Jersey. It is a global provider of delivery technologies, development, drug manufacturing, biologics, gene therapies and consumer health products. It employs more than 14,000 people, including approximately 2,400 scientists and technicians.

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