Details:
- Compensation: $70,000 - $75,000k
- Benefits: Medical, Dental, Vision
- Employment Classification: Direct Hire
- Status: On-Site
- Job ID: 20830
Primary Responsibilities
- Understand thoroughly all assigned studies through reading protocols, attending investigator meetings and start-up meetings, and coordinating with Principal Investigator
- Adhere strictly to the study protocol; obtain exemptions when necessary/appropriate
- Communicate protocol issues to CRO and/or Sponsor, Site Administrator, Director, Principal or Sub-Investigator
- Articulate all pertinent issues to the Pl or document by email/letter or during meetings
- Collect initial psychiatric and medical information by interviewing patients and by accessing other appropriate sources
- Ensure a flow of communication including telephone conferences between patient, study staff, referral sources, Sponsor and/or CRO, Monitor(s), Auditors and any marketing groups hired by the Sponsor
- Utilize various psychiatric rating scales and maintaining interrater reliability with other clinicians at K2 Medical Research
- Perform clinical tasks including, but not limited to, vital signs, height and weight, ECG, phlebotomy, specimen packaging
- Maintain timely K2 Medical Research source documentation as well as sponsor required information.
- Dispense and maintain accurate records of study medication
- Educate patients and family regarding their particular study and clinical drug trials in general.
- Complete all monitor and sponsor queries in a timely manner
- Provide appropriate community resource referrals to patients, caretakers, and family at conclusion of patient's participation in study
- Outstanding verbal and written communication skills
- Excellent interpersonal and customer services skills
- Strong time management and organizational skills In depth knowledge of industry regulations
- Proven ability to and foster mentoring relationships
- Ability to create momentum and foster organizational change
- Bilingual in Spanish/English highly desired.
- HS Diploma or GED Transcript required. Bachelor's degree strongly preferred.
- Prior experience in a clinical environment preferred. Experience in clinical research and Parkinson's (neurodegenerative disease) is ideal.
- Phlebotomy, LPN, RN, or other medical licensure or certification preferred.
- Strong working knowledge of GCP and FDA guidelines.
- Knowledge of medical terminology.
- BLS Healthcare Provider desired.