Clinician

JOB DUTIES:
Responsible for working collaboratively to implement one or more clinical protocols, with focus on study start-up and recruitment phases. Will be an integral study team member and key member of study feasibility team to identify, evaluate and select clinical sites and investigators. May be responsible for developing a site back-up plan that can be executed to support agreed timelines for study completion. Primary focus will be site communication to ensure site is knowledgeable on protocol requirements, recruitment and retention planning, solution and relationship building during the study start-up phase to optimize completion time for the clinical trial start-up phase and ensure site is ready to screen subjects immediately after initiation occurs. Work closely with sites to proactively identify, manage and timely resolve study start-up challenges, bottlenecks, site concerns. Potential Travel.

SKILLS:

SKILLS/QUALIFICATIONS:
Prefer 5+ years experience in clinical trial execution (would consider less experience for the right candidate).
Must have thorough understanding local and international regulations applicable to clinical trials.
The candidate experience should not solely be operational but rather have experience in alignment with our current position roles and responsibilities.
The candidate must have EXCELLENT communication skills and be thoroughly comfortable in speaking with employees of all levels.
Must be proficient in collaborative problem-solving skills.
Good clinical Practices (GCP).

REQUIRED EDUCATIONAL MINIMUM:
BA/BS.