CTM
Qualifications:
Bachelor’s degree or nursing qualification is required. Scientific/health care field preferred, but not required.
2+ years’ experience working in clinical research within a pharmaceutical company or CRO or similar organization.
Minimum of 2 years’ experience working as a Clinical Research Associate or monitoring experience.
Requires strong attention to detail in composing and proofing materials, establishing priorities, scheduling and meeting deadlines.
Must be able to work in a fast-paced environment with demonstrated ability to juggle multiple competing tasks and demands.
Ability to work successfully within a cross-functional team.
Strong knowledge of applicable computer and project management software packages.
Excellent written and oral communication skills.
Ability to interact with investigators, vendors, and internal colleagues.
Knowledge of current regulatory requirements and guidelines governing clinical research and GCP.
Ability to complete tasks to deadlines and resolve/elevate problems in a timely manner.