Conservation Research Coordinator Jobs in Florida

Assists in providing patient education and benefits and risks of participating in a clinical drug trial.

Determines protocol-related needs to conduct the trial and orders supplies and equipment.

Recruits and screens potential patients and obtains informed consent.

Designs organizational tools and forms to facilitate accurate data collection and recordkeeping.

Conducts in-service programs, summarizes study schedule to assist in understanding and implementing a protocol.

Schedules patient visits and laboratory and diagnostic test procedures.

Minimum Education And Experience Requirements

Experience in environmental education and outreach

(One year of relevant experience may be substituted for each year of required education.)

Master’s Degree in Biology, Planning, Environmental Sciences, Science Education, or related discipline.

Experience coordinating environmental marketing campaigns

Experience in creating social media content specific to environmental programs

Oversees and conducts the informed consent process on studies as appropriate (requires appropriate training and certification of human research subjects training).

Spearheads efforts to meet patient enrollment targets related to independent research studies. To that end, develops and implements various recruitment strategies.

Ensures accuracy of personnel transcribing data from paper case report form (CRF) into an electronic format.

Conducts study specific team meetings to ensure timely progress of patient enrollment and study activities.

Assist Principal Investigator with writing/editing abstracts and manuscripts as needed.

Assists in patient care coordination by assuring patients complete patient reported outcomes prior to office visits.

Assists in providing patient education and benefits and risks of participating in a clinical drug trial.

Determines protocol-related needs to conduct the trial and orders supplies and equipment.

Recruits and screens potential patients and obtains informed consent.

Designs organizational tools and forms to facilitate accurate data collection and recordkeeping.

Conducts in-service programs, summarizes study schedule to assist in understanding and implementing a protocol.

Schedules patient visits and laboratory and diagnostic test procedures.