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P arexel FSP is hiring multiple Site Care Partners across the US these are great opportunities for experienced CRAs seeking career advancement!!!!
Job Summary
accountable for site-level recruitment and operational success, and accountable for safeguarding the quality and patient safety at the investigator site.
The Site Care Partner acts as a Subject Matter Expert aimed to optimize country and site selection activities by proactively collaborating with key stakeholders and providing local intelligence to country outreach surveys, investigator strategies and client pipeline opportunities .
The Site Care Partner is the "face of the client" and therefore accountable for ensuring that sites receive necessary support and engagement, issues are resolved, and the clients reputation is upheld throughout study lifecycle .
Additionally, the Site Care Partner will coordinate with other roles and functions that will interface with study sites ( eg.
Study Monitor, Investigator Contracts Lead, Site Activation Partner, Clinician, etc.) thereby, optimizing communications and enhancing overall visibility into and confidence of quality of site level activities .
The Site Care Partner is responsible for site oversight utilizing and interpreting data from analytic tools, in conjunction with country intelligence to proactively identify risks to quality and compliance and to develop and implement mitigation plans to address these risks .
Job Responsibilities
Accountable for site start-up and activation
Deploy GSSO site strategies by qualifying and activating assigned sites
Supports processes to optimize country & site selection activities including review and assessment of the draft potential site list & provide PTA output for site selection .
Supports the Feasibility Strategy and Analytics Lead to ensure that high quality feasibility results are delivered
Collaborate with key stakeholders providing country / regional level input to country outreach surveys including protocol feasibility, country SOC and medical practices (as applicable).
Provide country / regional level input to country strategy, feasibility, and protocol design in collaboration with relevant Medical Affairs colleagues, and with input from external clinical experts as required .
Maintain a thorough knowledge of assigned protocols
Conduct study start up activities at the site level including but not limited to PTA, coordination of site activation checklist items, ICD finalization, SIV (as applicable), including management of issues that may compromise time to site activation.
Ensure all the site initiation activity including training per site activation checklist, collect and / complete necessary documentation / systems needed for site activation.
e.g. PSR, SART, ESRA, SAC, FU Letter, Planisware, ISF / eISF etc.)
Support country specific ICD review and deployment when applicable
Ensure follow up activities completion post PTA and SIV to ensure site readiness for FSFV
Partners with site monitor to ensure site monitoring readiness in anticipation of first subject first visit
Responsible for relationship building and operational oversight of the site
Provide study support on escalated site issues related to study delivery by coordinating communications and resolution efforts.
e.g., vendor, site contracts and payment issues etc.)
Ensure the strategy / approach for IP and ancillary supplies for sites and country requirement throughout the lifecycle of the study
Be accountable for effective site recruitment planning and delivery, consistent with global and / or country plan and local targets;
Responsible for enrollment support and ensure progress by responding to recruitment issues from investigators.
Maintain regular communications with investigator sites to gather status updates and drive delivery to study goals eg. recruitment, data entry timelines etc ).
Partner with local RA / CTRO / SAP to ensure timely completion on country / local registry when applicable
Accountable for study conduct and close-out
Act as operational point of contact for all site-level questions, liaising with and escalating to appropriate teams to respond and resolve questions.
Review Site Monitoring Reports
Support the site with revision and submission of ICD documents (and amendments).
Working with other roles, maintain system management (e.g., EDC , Shared Investigator Platform, Site Profile and other systems as applicable) at site level ensuring alignment across platforms.
During the conduct of the study, the Site Management Organization Assessment is reviewed with the site, when applicable, on an annual basis following site initiation and updated as needed.
Review and manage site practices that differ from client practices and liaise with study management and Business Process Owners as needed.
Maintain regular communications with investigator sites to gather status updates, informal and formal performance metrics, and study-level feedback.
Inform and educate investigator sites of client pipeline opportunities that may be a good fit.
Oversight and management of site deliverables to study targets, i.e. data cuts / sweeps, interim analyses, database locks, helping to oversee data is up to date and any other site-facing deliverables, i.
e. investigator signatures.
Follow the study oversight plan and proactively put in place mitigations for known / anticipated risks.
Assure quality and consistency in the delivery of monitoring
Drive monitoring efficiencies and best practices for study / region / program
Demonstrate leadership within the local clinical development environment with a goal to enhance client reputation in scientific leadership.
May act as a Subject Matter Expert on client systems and processes.
Actively pursue possible efficiencies and develop best practices in the delivery of activities for site performance throughout the life cycle to increase investigator / site satisfaction and strengthen site relationships
Ensures clear and open communication with Study Operations Manager
Support the site monitor to develop positive Investigator relationships throughout the life of the study and escalate any training or compliance concerns with Country Trials Manager and Study Management.
Responsible for proactively providing local intelligence
Provide input into country strategy / planning and site recommendations via intimate understanding of country / region, sites, processes and practices, and associated site performance metrics.
Provide input to cluster level intelligence for site strategy and support implementation of cluster-level strategy in collaboration with the Study Operations Manager / Global Study Manager
Provide regional exploration / territory development growing adjacent opportunities where possible.
Provide support to the Study Operations Manager / Global Study Manager to define local requirements for the importation / exportation processes of the investigational medical product and ancillary supplies.
Education
Bachelor's degree or RN in a related field or equivalent combination of education, training and experience (estimate at least 7 years experience )
Proficiency in local language preferred. English is required
Willingness to travel up to 70-75%
LI-REMOTE
Last updated : 2024-05-29
Full Time
Scientific Services
$34k-41k (estimate)
05/31/2024
08/30/2024
parexelcloud.com
BILLERICA, MA
15,000 - 50,000
1982
Private
MARK GOLDBERG
<$5M
Scientific Services
The job skills required for Care partner include Leadership, Collaboration, etc. Having related job skills and expertise will give you an advantage when applying to be a Care partner. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Care partner. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Care partner positions, which can be used as a reference in future career path planning. As a Care partner, it can be promoted into senior positions as a Home Care Aide III that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Care partner. You can explore the career advancement for a Care partner below and select your interested title to get hiring information.
If you are interested in becoming a Care Partner, you need to understand the job requirements and the detailed related responsibilities. Of course, a good educational background and an applicable major will also help in job hunting. Below are some tips on how to become a Care Partner for your reference.
Step 1: Understand the job description and responsibilities of an Accountant.
Quotes from people on Care Partner job description and responsibilities
According to resumes from both Care Partners and Homemakers, some of the skills necessary to complete the responsibilities of each role are similar.
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Health care providers may have patient partners who are part of their patients’ care teams.
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The Care Partner Program provides education for discharge planning to make sure patients go home as soon as possible and can stay there.
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They also provide care for their clients by helping them bathe, dress, brush their teeth, and other personal hygiene activities.
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Whenever a care partner helps a patient find something or solve a problem, the director of nursing will take charge.
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Step 2: Knowing the best tips for becoming an Accountant can help you explore the needs of the position and prepare for the job-related knowledge well ahead of time.
Career tips from people on Care Partner jobs
A patient can name one or two adults as Care Partners.
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Anyone the patient designates can become a care partner.
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Care Partners Need to Find and Celebrate the Positive Aspects of Providing care.
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Care Partners Should Learn as Much as Possible about the Disease.
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Care Partners Should Regularly Attend a Care Partner’s Support Group.
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Step 3: View the best colleges and universities for Care Partner.