Position Summary:
Clinical Research Associate ( Sr. CRA) is responsible for overseeing the execution of clinical trials at Investigative Sites. The Clinical Research Associate acts as a liaison between the study Sponsor, CRC and Investigative Sites. They will proactively identify and resolve clinical project issues and participate in process improvement initiatives as applicable. The CRA facilitates successful execution of studies by Investigative Sites and helps to ensure the rights, safety and welfare of human research participants as well as data integrity in clinical trials.
Key Responsibilities:

In addition to the above:

• Writes Clinical Trial Reports, analyzing and presenting trial results in a clear and accurate format.
• Reports, writes narratives, and follows-up on reported serious adverse events.
• Interacts and attends client meetings, as appropriate.
• Oversees activities of outside vendors.
• Mentors junior staff/CRAs.
• Quality oversight checks of monitoring.
• Performs other duties as assigned
• Perform other duties as assigned by management.

Qualifications:

• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience
• Minimum 5 years’ documented experience as a CRA; experience overseeing clinical trials in the pharmaceutical, hospital or CRO industry
• Ability to work and travel independently with minimal supervision
• Experience with numerous EDC systems
• Advanced knowledge of GCPs, ICH guidelines, FDA and other applicable regulations
• Specialized knowledge of CNS therapeutic areas (preferred)
• Proficient in Microsoft Office, Zoom and Adobe
• Excellent writing and verbal skills, English language proficiency
• Meticulous attention to detail
• Time management and ability to prioritize tasks

This position requires the ability to maintain an appropriate work pace, to perform varied tasks, to exercise logic and reasoning, to comprehend and follow instructions, and to make complex decisions. In addition to the above, this position requires the ability to sit for long periods of time and perform repetitive hand movements throughout the day. Specific vision abilities required by this job include close vision and the ability to adjust focus.
This position requires the ability to travel up to 70%.

ABOUT US:

Cognitive Research Corporation (‘CRC’) is a privately held, full-service contract research organization that specializes in Central Nervous System (CNS) product development for pharmaceutical, nutraceutical, biotechnology, and medical device companies. With offices in Florida and an integrated network of experienced research facilities, CRC is well-positioned to conduct clinical studies at any stage, Phase I-IV. To find out more, visit us at https://cogres.com/
If you’re ready to make a meaningful impact in the field of clinical research, apply now to our Contract Coordinator opening. Enjoy a dynamic work environment, opportunities for growth, and the chance to contribute to life-changing medical advancements.
Job Type: Full-time
Pay: $125,000.00 - $150,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Vision insurance

Medical Specialty:

• Neurology

Schedule:

• Monday to Friday

Work Location: Remot

Please refer the Job description for details