Personnel
PHARM Core 25 - Job Descriptions
Submitted by Tom Goddard on Fri, 2009-12-11 17:22The Basics
This standard requires URAC accredited companies to have job descriptions for all staff members. Those job descriptions must describe required background (education and experience), required competencies, licenses, and/or certificates, and describe the jobs' scope of role and responsibilities.
Management Tips
This standard typically is missed onsite by organizations that have not set minimum requirements for non-clinical staff members. Therefore, we recommend a complete internal audit, particularly by the HR departments of first-time applicants, of all the job descriptions to assure that they all (clinicaland non-clinical) have minimum requirements.
One other tip -- eliminate the words "or equivalent experience." They are, in URAC's view (and mine), meaningless. Describe what that equivalent experience might be, and you'll be fine.
URAC Accreditation Tips
Each of the elements of this standard carries a weight of only 2, indicating how distant job descriptions are from consumer protection, at least in URAC's mind.
The documentary requirements for this standard are straightforward -- submit up to 9 job descriptions of the staff members who do the bulk of the work in the areas that are the subject of the accreditation module(s). The onsite review is, as you might expect, a random selection of actual job descriptions, chosen from the staff directory.
CORE, Version 3.0 CORE 31 - Senior Clinical Staff Requirements
Submitted by Tom Goddard on Wed, 2009-09-16 11:03The Basics
This standard requires that the organization designated at least one senior clinical staff person to perform the functions described in Core 32. This standard sets forth at the required qualifications of that person. Those qualifications are:
- a current unrestricted clinical license,
- sufficient qualifications (e.g., experience, credentials, certifications) to conduct clinical oversight for the services provided by the organization,
- post-graduate patient care experience, and
- if the person is an M.D. or D.O., board certification.
This person typically is the medical or clinical director of your organization.
Management Tips
People in management positions should keep in mind that it is not sufficient that your senior clinician meet these minimum requirements. Rather, it is also required that the job description for that person, or some other document describing the person's role, require all of these qualifications.
The person occupying this position can be part time or full time.
URAC Accreditation Tips
All of the elements of this standard exit the requirement for board certification are mandatory. The board certification requirement carries the weight of three.
Documentation for the initial submission should include the designated senior clinician's job description and resume. In addition, you should submit either a program description or policies and procedures that described the senior clinician's role and accountabilities.
The on-site review will hinge on an interview of the designated senior clinician. In addition, the reviewer will examine the clinician's personnel file to assure that licensure, board certification, and work history are all documented appropriately.
CORE - 11 - Senior Clinical Staff Responsibilities
Submitted by Tom Goddard on Wed, 2009-09-16 10:54
The Basics
The senior clinician whose qualifications are set forth in Core 10 must, according to this standard, provide guidance and be responsible for all of the clinical aspects of the organization's program being accredited. In addition, the senior clinician must have periodic consultation with individuals in the field or licensed to deliver healthcare services without supervision, i.e. practitioners.
Management Tips
Again come up management personnel should make sure that the senior clinician's job description and resume are in order and in compliance with the standard. In addition, the organization's program description or policy and procedures that describe the clinician's role in accountabilities should be reviewed to make sure it complies with the standard.
URAC Accreditation Tips
All three elements of the standard, the one requiring that the senior definition be responsible for clinical aspects of the program, are primary in this 4-weighted standard.
The same documentation submitted for Core 10 should be submitted here. Similarly, the on-site review will turn on the interview of the senior clinician and a review of his/her personnel file.
Pharm Core 11 - Senior Clinical Staff Responsibilities
Submitted by Tom Goddard on Wed, 2009-09-16 10:37
The Basics
The senior clinician whose qualifications are set forth in Pharm Core 10 must, according to this standard, provide guidance and be responsible for all of the clinical aspects of the organization's program being accredited. In addition, the senior clinician must have periodic consultation with individuals in the field or licensed to deliver healthcare services without supervision, i.e. practitioners.
Management Tips
Again come up management personnel should make sure that the senior clinician's job description and resume are in order and in compliance with the standard. In addition, the organization's program description or policy and procedures that describe the clinician's role in accountabilities should be reviewed to make sure it complies with the standard.
URAC Accreditation Tips
One of the three elements of the standard, the one requiring that the senior definition be responsible for clinical aspects of the program, is mandatory. The other two are weighted 3.
The same documentation submitted for Pharm Core 10 should be submitted here. Similarly, the on-site review will turn on the interview of the senior clinician and a review of his/her personnel file.
Pharm Core 10 - Senior Clinical Staff Requirements
Submitted by Tom Goddard on Wed, 2009-09-16 10:27
The Basics
This standard requires that the organization designated at least one senior clinical staff person to perform the functions described in Pharm Core 11. This standard sets forth at the required qualifications of that person. Those qualifications are:
- a current unrestricted clinical license,
- sufficient qualifications (e.g., experience, credentials, certifications) to conduct clinical oversight for the services provided by the organization,
- post-graduate patient care experience, and
- if the person is an M.D. or D.O., board certification.
This person typically is the medical or clinical director of your organization. In a PBM, the general expectation is that he/she is a pharmacist,M.D., or D.O.
Management Tips
People in management positions should keep in mind that it is not sufficient that your senior clinician meet these minimum requirements. Rather, it is also required that the job description for that person, or some other document describing the person's role, require all of these qualifications.
The person occupying this position can be part time or full time
URAC Accreditation Tips
All of the elements of this standard exit the requirement for board certification are mandatory. The board certification requirement carries the weight of three.
Documentation for the initial submission should include the designated senior clinician's job description and resume. In addition, you should submit either a program description or policies and procedures that described the senior clinician's role and accountabilities.
The on-site review will hinge on an interview of the designated senior clinician. In addition, the reviewer will examine the clinician's personnel file to assure that licensure, board certification, and work history are all documented appropriately.
Pharm Core 9 - Staff Assessment Program
Submitted by Tom Goddard on Tue, 2009-09-15 15:34
The Basics
This standard requires that the organization operate a formal employee assessment program that contains two essential features: (1) an annual review, and (2) the review of documentation produced by the employee.
Management Tips
Some organizations have tried to meet the intent of this standard, and particularly the requirement that the appraisal include a review of documentation produced by the employee, by including in the template appraisal form a section allowing the employee to comment on his/her performance or on the supervisor's appraisal. It is increasingly clear that this will not suffice. Rather, your P&P and your template appraisal should be written to require and document that the supervisor looked a actual documentation produced by the employee in the course of performing his/her job.
URAC Accreditation Tips
This standard is weighted 3.
You need not submit an actual review in the initial, AccreditNet phase. A template will suffice. As usual, however, you also must submit a P&P that requires both the annual appraisal and a review of the documents produced by the employee.
The onsite review will involve an actual examination of the last one or two performance appraisals from the selected employees' personnel files.
Pharm Core 8 - Staff Operational Tools and Support
Submitted by Tom Goddard on Tue, 2009-09-15 15:33
The Basics
This standard requires that the organization provide the staff with both appropriate P&Ps and necessary clinical decision support tools. This means that each employee needs to know where to find the P&Ps and tools that help them understand the proper way to perform his/her job. Having a general notion that the applicable P&Ps are "somewhere on the shared drive" or "somewhere in the supervisor's office" is not enough. Each employee needs to have ready access to the applicable P&Ps and clinical tools.
Management Tips
The keys here are employee access and training. We strongly recommend against reliance on paper P&Ps and tools. Keeping a single copy of the current P&Ps and tools on a shared drive to which all employees have access is the best practice, and about the only way an organization can be sure that the correct version of P&Ps and tools are in the hands of the people who need them -- the employees.
URAC Accreditation Tips
Both elements of this standard carry a weight of 2.
Documentation for the standard is straightforward. The Master List of P&Ps should be submitted here, as it was for Pharm Core 3. In addition, the P&P or program description that describes the clinical decision support tools that the organization uses should be uploaded to AccreditNet.
The onsite review will test access as much as anything. Employees are likely to be asked something like, "if you have a question about how to do a certain aspect of your job, where would you find the proper procedure described?" The best answer will be if they can go directly to the P&P or clinical tool in question on their computer. The reviewer will need to see that the P&Ps are a useful tool for employees, not simply a document occupying space on a hard drive or a shelf.
Pharm Core 7 - Staff Training Program
Submitted by Tom Goddard on Tue, 2009-09-15 15:27The Basics
For a 7-minute video on URAC-required training, click here.
In any event, read on:
Management Tips
As you know, URAC has specific requirements for staff training that relate both to the content of staff training and its administration:
Content
Most of the explicit training requirements in the URAC standards are found in the Core and Pharm Core standards:
- Initial orientation and/or training for all staff before assuming assigned roles and responsibilities; (Core 7(a))
- Training in the P&Ps that apply to one's job is implied by Core 3(a), too
- Ongoing training, at a minimum annually, to maintain professional competency; (Core 7(b))
- Training in current URAC Standards as appropriate to job functions; (Core 7(c))
- Training in state and regulatory requirements as related to job functions; (Core 7(d))
- Conflict of interest; (Core 7(e))
- Confidentiality (Core 7(f)) and specifically HIPAA (Core 24)
- Training on identification and prevention of fraud and abuse, as appropriate to job functions; (Core 7(g))
- Delegation oversight, if necessary; and (Core 7(h))
In addition, training of employees in how to do their job consistent with company P&Ps and URAC standards is implied throughout the standards, via Core 3(a), 7(a), and 7(c).
Administration
- There must be documentation of all training provided for staff (Core 7(i))
- There must be a signed document acknowledging training on confidentiality issues (Core 24)
Some of this is company-wide training (e.g., confidentiality); some is department-specific (e.g., P&Ps on how to follow DM P&Ps.) Company-wide training is typically handled either through:
- company-wide meetings
- computer-based training modules required of all employees, or
- smaller, face-to-face trainings required of all employees.
Department-specific training is typically handled through
- modular computer-based training programs or
- departmental staff meetings
URAC Accreditation Tips
The best preparation for the URAC review is the substantive training described in the previous section. A staff member who knows his/her job as described by the applicable P&Ps, knows the URAC standards and state/federal regulations that apply to the job, and can retrieve the documents to be sought by the URAC reviewer is unlikely to get tripped up in a URAC review, even if they have no specific preparation for the onsite review process.
Additionally, the mock onsite review we conduct for our clients is valuable for staff members likely to be either interviewed or pulling documents during the onsite review. We spend a good portion of our time onsite not only conducting document-pulls and interviews as realistically as possible, but also counseling staff members on how to improve their performance for the actual review.
Pharm Core 6 - Credentialing
Submitted by Tom Goddard on Tue, 2009-09-15 15:18
The Basics
Pharm Core 6 requires the implementation of a P&P policy to conduct a verification the licenses and credentials of personnel (including consultants) who are required to be licensed and certified. This verification must occur upon hire, and no less frequently than 3 years after hire. Furthermore, the verification must be "primary source verification."
In addition, the standard places an obligation on such staff members to notify the organization of any adverse change in licensure or certification status. Finally, the organization's P&P on the topic needs to empower and require the organization to take corrective action when it learns of such adverse changes in the licensure or certification status.
Management Tips
It is important to note that the scope of the standard is broad: "licensed or certified personnel/consultants". While these are not defined terms, it is fairly clear that the URAC standard would sweep up a pretty broad array of licensed and certified people, not just employees.
Another thing to note is that the standard applies not only to licensure, but also to certification. This is particularly important with respect to accreditation standards such as case management, where certification might be a requirement. Be sure, therefore, that your process of verification, both as described in your policy and procedure and in practice, includes all certifications that might be required by the particular accreditation standards under which you are applying or by your own policies and procedures.
Finally, make sure not only that your policy and procedure on the subject imposes an affirmative obligation on the licensed personnel and consultants to notify the organization of adverse changes in licensure or certification status, but that everybody has been trained on this obligation. It would not be a good thing in an interview with a member of your staff if it became apparent that this requirement was unknown to licensed or certified staff members.
URAC Accreditation Tips
All three elements of this standard are mandatory.
The documentation required for the standard in the application is straightforward: job descriptions and a policy and procedure that addresses all three elements of the standard.
The documentation for the on-site review, on the other hand, is usually where the problems arise, if there are any. During the on-site review, the URAC reviewer will request a listing of all the members of the staff (at least those that are the subject of the review), randomly select several of the staff members, and ask to see their personnel files. The reviewer will be checking the job description and resume of each of the selected employees to see if the employees meet the requirements of the job as described in the job description. In addition, the reviewer will be looking for evidence that the employee's required licenses and certifications have been verified. Therefore, a best practice is for the organization to conduct periodic audits of all of its clinical staff members' personnel files to make sure that this is happening on ongoing basis, and particularly before the reviewer arrives.
Pharm Core 4, 5, 6, 7, 9, 24 -- Personnel File Contents
Submitted by Tom Goddard on Tue, 2009-09-15 15:10
Management Tips
What will the URAC reviewers find when they pull a random sample of your employees' personnel files? What should they find?
The URAC standards are rife with requirements that are likely to be evidenced in your personnel files. Because these standards are scattered throughout the Core module, it may not be immediately apparent what a URAC applicant should have in its personnel files.
Here's a short list, taken from an actual URAC onsite review agenda one of our clients just received from URAC, rearranged for clarity's sake:
- Evidence of Training
- Conflict of Interest Training
- Education on URAC Standards
- Continuing Education
- Orientation to job
- Staff Confidentiality Statements
- Regulatory Training
- Fraud & Abuse Training
- Other documentary requirements
- Annual Performance Review Process
- Job description/qualification evaluation
- Special requirements for clinical staff
- Scope of Practice Attestations
- License verification
- Certification verification
Particularly if your organization is a first-time applicant, you may be realizing that your personnel files don't have all these documents. What do you do now?
We recommend this four-step approach:
Conduct a thorough initial assessment. How bad is it? Take a random sample of your employee files and run down the above list for each one. Using this list to perform a gap analysis that will let you know the difference between what you have and what you need to have by the time the reviewers arrive.
Look for alternative sources of information. Now that you know what you need, find out whether you have that information, but not in the personnel files. For example, if your company has a centralized training tracking function, you may be able to take care of demonstrating compliance with all or most of the training documentation requirements through that tracking function.
Make a plan. With those items that are neither in the personnel files nor in a centralized function, you need to make a written plan, with specific time lines (that end before the reviewers arrive!), for pulling your files into compliance with the URAC standards. The discipline of going through such an exercise will be necessary, as may be the assistance of temporary help if your staff doesn't have the capacity to handle this task.
Look to the future. Once you have your personnel files in order and compliant with the URAC standards, make sure your policies and procedures are written in such a way to keep those files up-to-date. It will do no good to get the files into compliance this year if, for example, you are not doing annual performance reviews for all your employees and getting the results of those reviews into your personnel files.
Well-kept personnel files will help you meet the requirements of a significant number of important Core standards. Getting them into compliance may take some time, so start now.
