Veterans Preferred - Clinical Team Lead at HCA Healthcare in Nashville, TN

HCA Healthcare

๐Ÿ“Œ Nashville, TN
๐Ÿ•‘ November 22, 2020
๐Ÿท๏ธ FULL TIME
๐Ÿท๏ธ Healthcare
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Veterans Preferred - Clinical Team Lead

Military Veterans are Encouraged to Apply.

Description

SHIFT: Work From Home

SCHEDULE

Full-time.
Clinical
Team Lead
- Work From Home Sarah Cannon Development Innovationsis
a full-service contract research organization (CRO) that is uniquely
focused in oncology. Sarah Cannon Innovations offers strongscientific
leadership, access to patients through Sarah Cannon Research Institute's Site
Management Organization (SMO) and relationships with other clinical sites, and
experience in drug development and delivery of clinical trials from
First
- In
- Man through registration level studies, making us the partner of
choice for oncology. Our differentiator is strong operational delivery
in partnership with our Site Management Organization and physician leaders to
deliver your program efficiently.
This is a Work From Home
position and you can be located anywhere in the United States to be eligible
for this role. As the Clinical Team
Lead (CTL), you will be an integral member of the Project Team, having overall
responsibility and accountability for the execution and delivery of site
management and clinical operations strategy on a regional or global level, as
assigned. You will work closely
with the Project Manager to facilitate collaboration between Sarah Cannon
Development Innovations project teams, research sites and clinical trial
sponsors to advance common interests and achieve mutual goals. You will ensure that all clinical tasks meet client and Sarah Cannon expectations are complete in accordance with the contract, protocol, ICH-GCP guidelines and applicable Standard Operating Procedures (SOPs). You will oversee
investigator-initiated and/or sponsor trials from implementation to completion
with a key focus on managing project timelines for clinical deliverables,
oversight of investigative sites, and working with cross-functional teams on
data collection and site management. You will oversee planning and tracking of all assigned clinical activity from study start to completion, including investigative site recruitment/feasibility, essential document collection and reviewYou will track performance metrics for the study team (i.e., training, study visits, report and follow-up letter submission, and monitoring), reviewing and tracking enrollment and data entry timelines for sitesYou will work directly with data management and Clinical Research Associates (CRA) to monitor site accrual and data retrieval, while identifying and assistins CRA and Clinical Project Associate (CPA) teams with resolution of site specific issues.
Review monitoring reports and track ongoing site issuesYou will conduct monitoring and/or co-monitoring visits as determined by project needs and previous experience and training as a CRAYou will ensure TMF is set-up by CPA and maintained from study start to completion, perform regular audits of TMF documentsAs delegated by CPM, you will develop project status reports and communicate with all applicable team members in and outside the organizationYou may oversee and coordinate the implementation of projects; developing timelines and quality guidelines, coordinate team efforts on trial meeting deadlines and trial milestones depending on trial complexity or stageYou will create a variety of reports, documents, training tools, and correspondence as needed to assist participating trial sites and for internal purposes in the ongoing monitoring and evaluation of the projects progress.
Communicate and escalate unresolved issues at the appropriate time and to the appropriate level of managementYou may be required to travel up to 20% for meetings, site visits, and/or attendance at conferences.

Qualifications

For
this role, you must have:
A Bachelor's Degree (4
year program)3 years of experience in
clinical research as a CRA or similar research/healthcare professional.
Experience in writing
technical documents.
Experience in clinical
trial set-up, maintenance, and close-out It is
preferred that you have: 3-4 years of experience in a clinical trial environment, oncology CRA experience preferred.
Significant experience writing technical documents such as study plans.
Experience in clinical trial set-up, maintenance, and close-out Do you find this opportunity compelling,
if so we encourage you to apply?
We promptly review all applications. If you
are highly qualified you will hear from one of our recruiters. We are actively
interviewing so apply today. We
offer you an excellent total compensation package, including competitive
salary, excellent benefit package and growth opportunities. We believe in our
team and your ability to do excellent work with us. Your benefits include 401k,
PTO, medical, dental, flex spending, life, disability, tuition reimbursement, employee
discount program, and employee stock purchase program.
We would love to talk to you about this fantastic opportunity. We are an equal opportunity employer
and value diversity at our company. We do not discriminate on the basis of
race, religion, color, national origin, gender, sexual orientation, age,
marital status, veteran status, or disability status. Notice Our Company's recruiters are here to help unlock the next possibility within your career and we take your candidate experience very seriously. During the recruitment process, no recruiter or employee will request financial or personal information (Social Security Number, credit card or bank information, etc.) from you via email. The recruiters will not email you from a public webmail client like Gmail or Yahoo Mail. If you feel suspicious of a job posting or job-related email, let us know by clickinghere.
For questions about your job application or this site please contact HCAhrAnswers at 1-844-###-#### option 1.

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Job Expires: December 22, 2020

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