Contract Senior Clinical Research Associate

Job Title: Freelance Senior Clinical Research Associate

Job Location: South-west England, UK (Home-based)

Job Overview:

Caidya, a global mid-sized CRO, is currently seeking an experienced freelance/contractor CRA to join our team in the UK, monitoring sites predominantly located in the South West of England. We are looking for someone with 0.7FTE - 1FTE, for an immediate start, ideally with experience in cardiology and oncology studies.

Job Duties and Responsibilities:

• Provides support to Project Team and Clinical Operations Team.
• Maintains strong working knowledge of protocols and Monitoring Plans for assigned projects.
• Demonstrates strong written and verbal communication skills.
• Serves as primary contact for assigned research sites.
• Verifies that the investigator, staff, and site facilities remain adequate throughout the trial period.
• Responsible for the scheduling and conduct of pre-study visits, initiation visits, interim monitoring visits and close-out visits according to the Monitoring Plan.
• Ensures research sites conduct studies according to protocol requirements or investigational plan and applicable regulations and guidelines.
• Verifies the rights and well-being of trial subjects are protected.
• Reconciles site regulatory binder assuring collection and completeness of regulatory documents.
• Collects and ensures completeness of all essential regulatory documentation from sites from study start-up through close-out.
• Verifies that written informed consent was obtained before each subject’s participation in the trial.
• Verifies that the investigator is enrolling only eligible subjects.
• Performs source data verification against Case Report Form/Electronic Data Capture entries in compliance with the Monitoring Plan. Ensures accurate and complete data and that corrections are appropriately documented by authorized site staff.
• Verifies the quality of all recorded data. Issues and ensures timely resolution of all data queries remotely or at investigator site.
• Performs Investigational Product accountability, including product storage, inventory, return/destruction, and dispensing/receipt records.
• Verifies and supports the recording and reporting of adverse events/serious adverse events. Ensures all types of adverse events are reported and tracked per regulatory requirements and the Monitoring Plan.
• Ensures that sites have sufficient project specific supplies.
• Manages investigative sites in respect to the trial conduct and motivates sites to meet study goals.
• Communicates deviations from the protocol, SOPs, and/or GCP, to the investigator, and project management team and takes appropriate action to prevent recurrence.
• Delivers high quality written trip reports, confirmation and follow-up letters within timelines of SOPs and monitoring plans.
• Participates in site audits, as requested.
• May conduct site and study feasibility assessments.
• Uphold the confidentiality agreements with all clients and colleagues outside Caidya.
• Pays attention to signals of fraud, misconduct and escalates per Caidya SOP.
• Work according to the project-specific timelines and budget agreement, which has been agreed upon with the sponsor. Accurately document the time spent per project in the CPWW time allocation system.
• May conduct project co-monitoring visits and/or training visits.
• May serve as site contact for protocol clarifications and subject enrollment.
• Attends and participates in team teleconferences/meetings.
• Attends investigator meetings.
• Demonstrates flexibility and adaptability.
• Proactively identifies, manages, escalates (as needed) and resolves site issues effectively and independently.

Supervisory Responsibilities: None

Job Requirements:

• Education
  • 4 year college graduate, preferably with a healthcare or life science degree.
  • In lieu of a degree, candidates with 3 or more years of relevant clinical research experience in pharmaceutical or CRO industries will be considered.
• Experience
  • Minimum of 3 years of experience in on-site monitoring of clinical studies.
• Skills/Competencies
  • Strong written and verbal communication skills
  • Strong interpersonal skills
  • Expert monitoring skills to independently conduct all types of site monitoring visits
  • Good documentation skills; good command of English and the local language in the area of activity (reading, writing, understanding)
  • Strong computer skills, including Microsoft Office
  • Comprehensive knowledge of GCP/ICH guidelines
  • Proficiency in medical terminology
  • Able to exercise judgment within defined procedures and practices and to determine appropriate action independently.
  • Exceptional attention to detail
  • Superior problem-solving skills
  • Assist in training/mentoring guidance and presentation skills.
  • Ability to work in a matrix environment
  • Exceptional time management and organizational skills
• Capabilities
  • Ability to drive an automobile and have a valid driver’s license, if applicable.
  • Valid passport required in the case of international business travel.
  • Ability to travel.

The company will not accept unsolicited resumes from third party vendors.