Must be a licensed health-care professional (i. e. , registered nurse); or equivalent work experience. Read, write and speak fluent English; fluent in host country language required. 2+ years of clinical monitoring experience required.
Ability to travel as necessary (approximately 10%) Bachelor’s degree or registered nurse, In lieu of degree or RN, eight years of relevant experience. Six years of progressively responsible Clinical or Data Management experience, with at least four years of Data Management experience.
Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i. e. , registered nurse); or equivalent work experience required. Read, write and speak fluent English.
Must be a licensed healthcare professional (ie, registered nurse); or equivalent work experience required. 2 years of clinical monitoring experience with oncology or equivalent combination of education and experience. Must be legally authorized to work in the United States.
BS/BA or Nursing background with at least 6 years in Clinical Research, or equivalent combination. Strong knowledge of ICH-GCP and FDA, proficient with CTSM, EDC systems. Excellent communication, management, leadership and decision-making skills.
e. registered nurse); or equivalent work experience required. Minimum 3+ years of clinical research required as CM, RSM or PM. Working knowledge of FDA Guidance Documents / EU Directives / ISO14155 regulations, drug / device development, and clinical monitoring procedures.
Must be a licensed health care professional (i. e. registered nurse) or equivalent work experience required. Must read, write and speak fluent English and be fluent in host country language. Strong experience in clinical trial management as a CM. Experience in managing complex or global trials.
Bachelor's Degree, preferably in life science or nursing, Statistics or Computer Science or equivalent. Minimum 5 years relevant data management experience. Rave or Inform Experience. Proven data management skills. Excellent verbal and communication skills.
Degree in Life Science, nursing background and/ or combination of education/experience. Minimum 5+ years experience in project management for clinical trials. Prior experience attending bid defenses and kick-off meetings. Excellent written and verbal English communication skills.