CLINICAL OUTCOMES MANAGER manages the collection and analysis of clinical outcomes data to develop clinical process improvement initiatives. Oversees staff who gather data on performance metrics and facilitates the review of clinical program effectiveness. Being a CLINICAL OUTCOMES MANAGER provides advanced analyses and reports on clinical outcomes data. Evaluates and summarizes patient data to ensure that care is provided in accordance with clinical guidelines and organizational standards. Additionally, CLINICAL OUTCOMES MANAGER identifies areas for improvement and assists leaders/physicians in developing strategies to improve performance. Requires a bachelor's degree in nursing or healthcare related area. May require a Registered Nurse (RN) license. Typically reports to a director. The CLINICAL OUTCOMES MANAGER typically manages through subordinate managers and professionals in larger groups of moderate complexity. Provides input to strategic decisions that affect the functional area of responsibility. May give input into developing the budget. To be a CLINICAL OUTCOMES MANAGER typically requires 3+ years of managerial experience. Capable of resolving escalated issues arising from operations and requiring coordination with other departments. (Copyright 2024 Salary.com)
Clinical Research Site Manager
Hattiesburg, Ms
Position
Summary for Clinical Research Site Manager
Site Manager will be responsible for the
supervision of the Hattiesburg research site ensuring processes are implemented according to
the direction of leadership. The Manager will also be responsible for the
effective execution of site protocols, regulatory compliance, and providing daily
direction to the site’s Clinical Research Staff. The Clinical Research Manager will help build
the clinical team in Hattiesburg ensure that the
Clinical Research staff has the resources necessary to efficiently and
effectively conduct each study.
Hours: 8am - 5pm or 9am - 6pm
Onsite: 100% but could work from home a couple of days a week (flexibility)
Benefits for
Clinical Research Site Manager
· Competitive Compensation
· Benefits:
o 401K
o Health Insurance
o Generous PTO
o 1 – 2 Direct Reports
Roles and
Responsibilities for Clinical Research Site Manager
· Facilitate the overall successful
implementation of and compliance with all of the
processes, SOPs, work instructions, and best practices
· Maintain
site staff compliance with all regulatory, protocol, and federal
rules/regulations/requirements
· Work with the Director of
Site Operations to implement and manage action plans required to reach the goals
for clinical studies
· Train staff on internal
processes and procedures as well as ensure compliance providing feedback and
coaching as required
· Ensure
that the clinical research team has proper training and resources necessary to
successfully perform and complete the research projects
· Conduct
individual quarterly reviews with staff members to ensure that individual goals
and expectations are being met as well as meeting the business goals and
objectives.
· Fully manage Dayton -based staff, including PTO requests, attendance, schedules and other needed
tasks. Will work with and receive
direction from Corporate Human Resources regarding payroll/time and attendance
reporting, employee relations matters, benefit matters and other staff
management processes.
Education
and Experience for Clinical Research Site Manager
· RN
or Bachelor of Science Degree minimum
· Minimum of 5 years of clinical
research experience
· Minimum of 2 years prior Management experience
preferred
Knowledge
and Skills Required for Clinical Research Site Manager
· Solid aptitude in process
implementation and the management of processes and procedures
· Experience building & leading
teams, providing direction, coaching and motivating staff
Clear All
0 CLINICAL OUTCOMES MANAGER jobs found in Gulfport, MS area