パレクセルでの仕事
パレクセルは、臨床開発の上流から下流までのそれぞれの専門領域で、国内外の多くのお客様に高度なソリューションを提供するプロフェッショナル集団です。 パレクセルは、新しい薬や治療法を、それらを必要としている人々にいち早く届けることを目指し、日々の業務に取り組んでいます。
Research Associate
応募 求人ID 65531BR ロケーション ボルチモア, メリーランド州 仕事内容
Key Accountabilities:
Accountability Supporting Activities
Detailed Knowledge • Has detailed knowledge of the study protocols and acceptable performance of quizzes.
• Follows medical records procedure.•
Recruitment • Recruits study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments.
Enter study participants information into ClinBase™ • Enters study participants in the study participant tracking system, ClinBase™, and study logs, maintains appointment calendars, and operates company information systems and computer programs.
Conducts screening visits • Conducts screening visits and study protocol specific study participant visits, assists staff physicians in assessment of concomitant medications, adverse events, lab results and other test results.
• Performs appropriate psychometric and efficacy testing according to study protocol.
• Receives authorized sign-off to verify accuracy of all study participant visits.
• Prepares/monitors study supplies and stock levels in clinic/hospital.
• Labels, inventories and sends plasma samples.
• Problem solves study participant issues as they arise.
• Ensures basic study participant safety is provided
Assists and identifies issues while assuming appropriate role in position • Assists with Monitor visits (i.e., room set up, etc.).
• Identifies issues that need Sponsor approval and brings these to the attention of the CRC.
• Maintains supportive, flexible manner internally with management, coworkers/team members.
• Maintains and updates knowledge of Clinical Operating Guidelines and their proper application.
• All other duties as assigned.
• Assumes appropriate role with study participants and caregivers.
• Attends and assists with start-up and flow sheet meetings.
• Completes Case Report Forms (CRF) in a timely manner.
• Assures quality and accuracy of source and CRF documentation.
• Complies with Quality Management (QM) department guidelines and performs corrections for QM, CRC and Monitor/Sponsor Representative in a timely manner.
• Maintains accurate accountability for petty cash.
• Exhibits professional demeanor at all times in external interactions with Sponsors/Sponsor Representatives.
• Demonstrated competency in all research-related tasks.
• Strong interpersonal, written/verbal communication and organizational skills.
• Knowledge and skill in techniques of good clinical judgment and good nursing care/adequate technical vocabulary (if RN/BSN).
• Ability to effectively manage time and multi-task.
• Demonstrated knowledge and skills necessary to provide care appropriate to the age and/or indication of the study participants.
• Ability to function well in a team environment.
• Computer proficiency preferred.
Knowledge and Experience:
• Prior clinical research experience, floor nursing, and/or psychiatric experience a plus.
Education:
• BS, BA in a related field or equivalent work experience.
• BSN, RN, foreign MD or Master’s Degree a plus.
応募あとで応募 Accountability Supporting Activities
Detailed Knowledge • Has detailed knowledge of the study protocols and acceptable performance of quizzes.
• Follows medical records procedure.•
Recruitment • Recruits study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments.
Enter study participants information into ClinBase™ • Enters study participants in the study participant tracking system, ClinBase™, and study logs, maintains appointment calendars, and operates company information systems and computer programs.
Conducts screening visits • Conducts screening visits and study protocol specific study participant visits, assists staff physicians in assessment of concomitant medications, adverse events, lab results and other test results.
• Performs appropriate psychometric and efficacy testing according to study protocol.
• Receives authorized sign-off to verify accuracy of all study participant visits.
• Prepares/monitors study supplies and stock levels in clinic/hospital.
• Labels, inventories and sends plasma samples.
• Problem solves study participant issues as they arise.
• Ensures basic study participant safety is provided
Assists and identifies issues while assuming appropriate role in position • Assists with Monitor visits (i.e., room set up, etc.).
• Identifies issues that need Sponsor approval and brings these to the attention of the CRC.
• Maintains supportive, flexible manner internally with management, coworkers/team members.
• Maintains and updates knowledge of Clinical Operating Guidelines and their proper application.
• All other duties as assigned.
• Assumes appropriate role with study participants and caregivers.
• Attends and assists with start-up and flow sheet meetings.
• Completes Case Report Forms (CRF) in a timely manner.
• Assures quality and accuracy of source and CRF documentation.
• Complies with Quality Management (QM) department guidelines and performs corrections for QM, CRC and Monitor/Sponsor Representative in a timely manner.
• Maintains accurate accountability for petty cash.
• Exhibits professional demeanor at all times in external interactions with Sponsors/Sponsor Representatives.
Qualifications
Skills:• Demonstrated competency in all research-related tasks.
• Strong interpersonal, written/verbal communication and organizational skills.
• Knowledge and skill in techniques of good clinical judgment and good nursing care/adequate technical vocabulary (if RN/BSN).
• Ability to effectively manage time and multi-task.
• Demonstrated knowledge and skills necessary to provide care appropriate to the age and/or indication of the study participants.
• Ability to function well in a team environment.
• Computer proficiency preferred.
Knowledge and Experience:
• Prior clinical research experience, floor nursing, and/or psychiatric experience a plus.
Education:
• BS, BA in a related field or equivalent work experience.
• BSN, RN, foreign MD or Master’s Degree a plus.
