Clinical Coordinator Jobs

About The Position

Requirements

• Bachelor's degree preferred but not required.
• Preferably at least 2 years of experience as a Clinical Research Coordinator, plus 1–3 or more years of experience in clinical research or biological research.
• Exceptional knowledge of clinical research methods.
• Strong management and leadership skills.
• Demonstrated ability to collaborate and align with operations.
• Excellent oral and written communication skills.
• Excellent computer skills, including Office 365 products.
• Experience writing and reviewing Standard Operating Procedures.
• Strong problem-solving, risk-assessment, and impact-analysis abilities.
• Demonstrated experience in process improvement.
• Strong negotiation and conflict-management skills.
• Ability to multitask and prioritize competing demands.
• Ability to think independently and influence when appropriate.
• Ability to drive and daily availability of an automobile.
• Ability to properly lift 35 pounds and occasionally more than 35 pounds.

Nice To Haves

• Bachelor's degree.
• At least 2 years of experience as a Clinical Research Coordinator.
• At least 1–3 or more years of experience in clinical research or biological research.

Responsibilities

• Read, understand, and carry out protocol-specified patient visits and procedures.
• Document patient assessments, observations, test results, and other study information according to federal regulations, protocol requirements, and GCPs.
• Obtain informed consent in accordance with federal regulations, GCPs, and IRB requirements.
• Recruit qualified study participants to meet enrollment obligations within sponsor timelines while following applicable medical ethics, IRB, GCP, and ICH requirements.
• Complete required training in a timely manner.
• Schedule and conduct patient visits according to protocol requirements and timelines.
• Maintain accurate and complete written source documentation of patient visits and protocol-related activities.
• Complete sponsor-generated case report forms, electronic case report forms, and worksheets accurately.
• Maintain confidentiality of patient and protocol information in accordance with applicable confidentiality agreements and HIPAA regulations.
• Promptly report adverse events to a supervisor and/or Principal Investigator or Sub-Investigator as appropriate.
• Report serious adverse events to the sponsor within 24 hours of becoming aware of them, and notify the supervisor and/or Principal Investigator or Sub-Investigator.
• Account for clinical trial materials and ensure appropriate quantities are available for study conduct.
• Maintain and document ongoing communication with the Team Lead I, Team Manager, Principal Investigator, Sub-Investigators, and others assisting with trials, as required by protocols and company policies.
• Attend required training courses and conferences to remain current on regulations and company policies.
• Pursue educational opportunities to increase knowledge of clinical research and relevant rules and regulations.
• Attend Investigator Meetings and other training as directed.
• Perform study-related duties in a time- and cost-effective manner and in adherence with company policies.
• Perform duties safely and prudently.
• Represent Flourish Research professionally and courteously when interacting with staff, sponsors, IRBs, patients, and medical and nursing staff.
• Perform other duties as assigned by management.

Benefits

• Health insurance
• Dental insurance
• Vision insurance
• 401(k) with a 100% employer match on the first 4% of employee contributions
• Tuition reimbursement
• Parental leave
• Employee referral program
• Employee assistance program
• Life insurance
• Disability insurance
• Generous PTO covering vacation, sick, and personal days
• Eight paid holidays