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Experienced office based clinical MEDICAL ASSISTANT needed with an outpatient clinical research organization on a Full-Time basis. Clinical Research experience preferred, but not required.
Qualified candidate will assist the research team in the implementation and conduction of clinical trials per federal, state and institutional guidelines by performing tasks delegated by research team members including investigators, managers and coordinators. Responsibilities during all phases of trials from pre-study implementation through study closure are included in the scope of this position.
Candidate must have a willingness to learn all aspects of all Phase I-IV studies. Needs to be team oriented, outgoing, self-starter and have an eagerness to learn. Ability to work independently once fully trained. Must be willing to travel for training and between offices as necessary. Pay based on experience.
MEDICAL ASSISTANT
- Posted: April 19, 2024
- Salary:US$20.00 - US$25.00 per hour + Medical, Dental, Vision, 401k, sick time
- Location:Scottdale
- Job type: Permanent
- Discipline:Life Sciences
- Reference:225657_1713544947
- Work Location:On-site
Job description
Description
Experienced office based clinical MEDICAL ASSISTANT needed with an outpatient clinical research organization on a Full-Time basis. Clinical Research experience preferred, but not required.
Qualified candidate will assist the research team in the implementation and conduction of clinical trials per federal, state and institutional guidelines by performing tasks delegated by research team members including investigators, managers and coordinators. Responsibilities during all phases of trials from pre-study implementation through study closure are included in the scope of this position.
Candidate must have a willingness to learn all aspects of all Phase I-IV studies. Needs to be team oriented, outgoing, self-starter and have an eagerness to learn. Ability to work independently once fully trained. Must be willing to travel for training and between offices as necessary. Pay based on experience.
Primary responsibility is to screen, enroll and follow study subjects ensuring protocol compliance and close monitoring while the subjects are on study. Responsible for all data collection, source documentation, completing study specific case report forms, and submission of adverse experience reports.
- Working knowledge of medical and research terminology.
- Working knowledge of federal regulations, good clinical practices (GCP).
- Ability to communicate and work effectively with a diverse team of professionals.
- Excellent organizational and prioritizing capabilities.
- Strong computer skills with demonstrated abilities using clinical trial database, electronic data capture, and MS Word or Excel.
- Excellent interpersonal skills, detailed -oriented and meticulous.
- Excellent professional writing and communication skills.
- Ability to work independently in a fast pace environment with minimal supervision at off site facilities.