Position Summary:

The Clinical Trial Manager is responsible for managing the clinical and operational activities of assigned clinical studies. This is accomplished by ensuring all projects are completed on-time and on-budget while following all company policies, Standard Operating Procedures (SOPs) and applicable regulatory guidelines. Plan, develop, and follow systems and procedures to ensure optimum compliance in accordance with GCP/ICH guidelines and FDA regulations. Ensure operating quality and efficiency.

Location: Remote

Position Summary:

The Medical Monitor (MM) plays a critical role in overseeing the safety and efficacy of clinical trials, ensuring compliance with regulatory requirements, providing medical oversight, and performing medical data reviews to ensure patient safety and data integrity. Collaborates with Project Manager, Safety/Pharmacovigilance (PvG), Data Management, Biostatistics, QA, Principal Investigator and Sub-investigators, Site Coordinators, the Data Monitoring Committee (DMC), and any other group that directly or indirectly protects the safety of study participants.

Location: Remote

Position Summary:

The Senior Proposal Manager will lead, manage and execute the full life cycle of proposal development activities for Clinical Trials Proposals, and support budget generation. Manage and develop the contract development process to support an efficient, high quality, and timely RFP and contracting process. This process may include pricing, developing proposals, work orders, change orders, start-up agreements, and other contracts that support the delivery of sponsor studies.

Location: Remote

Position Summary:

The Director of Business Development (DBD) is responsible for supporting new business development and sales objectives to support the long-term growth of CRC. They will target the addressable biopharmaceutical market in CNS by maintaining industry awareness of biopharmaceutical accounts, their drug pipeline milestones, and potential opportunities that are a match for CRC. They are new and repeat business goal-carrying leaders within CRC and will directly prospect target accounts to arrange initial meetings, qualify opportunities, organize the sales strategy, and bring opportunities to closure. They actively prospect potential accounts and discuss their company and its development plans and ways where CRC can support. They organize sales campaigns with support and input from CRCs scientific, medical, operational, and biometric experts. They organize proposals and proposal presentation meetings. They work with commercial leadership, proposals, finance, and legal to facilitate the closing process. They participate in meetings to review sales goals and present strategies to close new business.

Location: Remote

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.

Location: Remote

Position Summary:

The Clinical Trial Assistant (CTA) supports the execution of clinical studies at Cognitive Research Corporation (CRC), a CNS-focused, full-service CRO. This role assists with Trial Master File maintenance, site communication, and study documentation to ensure accuracy, compliance, and efficiency across all trial phases. Ideal candidates are organized, detail-oriented, and eager to grow their career in clinical research.

Location: St. Petersburg, FL