Clinical Research Coordinator in Media, PA (19063)
Responsibilities:
- Study Coordination: Oversee the execution of study protocols under the guidance of the Principal Investigator.
- Participant Procedures: Handle participant-related tasks including scheduling and conducting visits, documenting via source materials, collecting vitals (such as height, weight, ECG), and performing phlebotomy/specimen collection. Serve as the primary contact for participant inquiries and manage investigational products.
- Data Management: Enter data accurately and maintain organized study files.
- Sponsor Communication: Liaise with sponsors, addressing their requests and ensuring smooth communication.
- Travel: Participate in new study start-up activities, requiring travel up to four times a year.
Candidate Profile:
- Highly Organized: Able to manage multiple responsibilities in a fast-paced and sometimes high-pressure environment.
- Adaptable Under Stress: Capable of handling sudden challenges and ambiguous situations calmly and efficiently.
- Personable: Friendly and approachable, fostering positive relationships with participants and team members.
- Independent and Reliable: Trusted to work autonomously while maintaining high standards.
- Effective Communicator: Able to work well within a team and clearly convey information to sponsors, participants, and colleagues.
- Multitasker: Skilled at prioritizing tasks and managing competing demands.
- Hierarchical Awareness: Comfortable working within established organizational structures.
Qualifications:
- Education: Bachelor's degree, Registered Nurse (RN), or higher.
- Tech-Savvy: Proficient with technology and able to independently navigate various programs and systems.
- Vaccination Requirement: COVID-19 vaccination required.
- Commuting Ability: Must be able to travel to West Chester, PA, and Media, PA.
Additional Details:
Location: Media, PA (19063) - This position will require you to travel to West Chester, PA
Pay: $45,000-$65,000 Annual Salary
Hours: Monday-Friday; Normal Business Hours; Onsite 5 Days a week
Employment: ~6 month (1,040 Hours) contracted probationary period into direct hire / permanent position
Requirements: Bachelor's Degree; 1+ Years of Clinical Research Coordinating experience
