Healthcare and Clinical Positions2616N PhD CBT Psychologist Generalist GTA
2615N Medical IME Assessor Recruiting Specialist ON
2614N Intake Supervisor IME GTA
2612N Medical Coder Massachusetts
2610N Canadian Licensed Veterinarian QC
2605N Medical Device Clinical Research Manager Boston area
2601N Medical Physicist - Radiation Physics Therapy Illinois
2585N Cerner Patient Accounting/Billing Analyst West Virginia
2451 Sr. CRO Toxicologist Study Director Montreal
Job ID: 2616N
Position: 2616N PhD CBT Psychologist Generalist GTA
Location: Oakville, ON
Description: Psychology clinic in the Oakville/Mississauga area, part of the Toronto, ON GTA, is looking for a CBT PhD Psychologist / Psych D. Must be registered in good standing with the CPO. Generalist. Contractor, who will bill the clinic for hours spent. Working hours flexible - 2 to 5 days as desired. Some evenings. Diagnosis, treatment, reports.
Job ID: 2615N
Position: 2615N Medical IME Assessor Recruiting Specialist ON
Location: Toronto, ON
Description: Toronto area IME requires a Medical Assessor Recruiting Supervisor to manage all related duties. An IME client in Toronto is recruiting for a Supervisor Roster Assessor Relations and Recruiting Specialist. ROLE AND RESPONSIBILITIES: - Hiring and onboarding of medical assessors. - Manage all people working in Assessor Recruitment and Relations Department. - Ascertain that medical assessors maintain good standing within their colleges, are HCAI registered, and have current profiles. - Training, supporting performance, and assessor-related escalation management. - Timely scheduling of patients and appointment confirmation via Smart Simple booking system. - Fee and profit matters. - Weekly assessment fee and roster reporting. REQUIREMENTS: B.Com. OR proven organizational management experience. 3 years' related work experience in an IME, in an assessment management role.
Job ID: 2614N
Position: 2614N Intake Supervisor IME GTA
Location: Toronto, ON
Description: Toronto IME clinic requires an Intake Supervisor, responsible for daily operations related to Admin and Intake. ROLE: Daily Admin and Intake issues. Training Admin and Intake personnel - Receptionists, Document Specialists) re duties and POPs. Keep training materials up to date. Internal intake and admin audits. Help coordinate intake meetings, balance workload. Keep track of performance, attendance, productivity. REQUIREMENTS: 2 to 3 years supervisory experience working in MVA and experience with SABS. Excellent knowledge of medical disciplines and terminology. Able to scrutinize reports and records. Great interpersonal, problem solving, decision making skills.
Job ID: 2612N
Position: 2612N Medical Coder Massachusetts
Location: Boston, MA
Description: Boston, MA healthcare facility looking for a Medical Coder - contract position. ROLE, RESPONSIBILITIES, REQUIREMENTS: Make sure all encounter forms used by providers and practices are up to date. Distribute info about new codes and/or coding policies. Set up department processes and controls to comply with Professional Coding, CMS, HIPAA, State of Massachusetts, and national payor coding guidelines. Bring providers and clinical staff up to date on new documentation. Ensures the confidentiality of personal health information via doctor network policies related to the release of medical record information, record retention, and HIPAA privacy and security. Need knowledge about coding Medicare Annual Wellness Visits.
Job ID: 2610N
Position: 2610N Canadian Licensed Veterinarian QC
Location: Quebec , QC
Description: Quebec City, QC well-established, large veterinary clinic is looking for a licensed veterinarian. You will be joining a group of several dozen colleagues, many focused on the emergency medicine side of this sizeable clinic. REQUIREMENTS: DVM and license to practise in Canada and eligible to write the necessary QC exams. Must have graduated from an accredited college of veterinary medicine. Vets with emergency room (ER) / intensive care experience of great interest. Must be bilingual (French as one of the languages) or willing to learn French asap. Experience important but new licensed grads are welcome. Licensure: 1. To practice veterinary medicine in Canada in general, students must obtain a licence by passing the North American Veterinary Licensing Exam (NAVLE). 2. The National Examining Board (NEB) is responsible for the administration, in Canada, of a 3-part veterinary licensing examination process. Completion of the exams is a requirement to be eligible to apply for license from any of the provincial veterinary licensing bodies. 3. In addition, to practice in the Province of QC, you must also pass the Ordre des mˇdecins vˇtˇrinaires du Quˇbec (OMVQ) exam.
Job ID: 2605N
Position: 2605N Medical Device Clinical Research Manager Boston area
Location: Boston, MA
Description: Our client, a leader in the medical device arena, is presently conducting clinical trials on some of their newer laser devices. They require a clinical research manager / project manager to assume a leadership role in the supervision of trials at a number of sites in the Boston area. ROLE AND RESPONSIBILITIES: - Leading, coordinating a variety of trials at 6 to 10 different clinical sites, at different device life cycle stages - Help study directors / CRAs plan/design all protocols and related study documents. - Interact with CRAs, Clinical Data Managers, physicians, nurses to coordinate their studies, monitor progress, and prepare status reports. - Bearing FDA compliance in mind, make sure trials comply with GCP requirements. - Help team work with Regulatory Affairs; set up audit procedures to make sure studies meet regulatory objectives and that the data will support regulatory filings. - Together with the data managers, make sure that only "clean" data appears in the database. Note that this client runs a paper based system, so the process should be clean and simple. - Able to take a more hands-on role in coordinating study sites based on resources and requirements. REQUIREMENTS: B.Sc. (Nursing B.Sc.N) preferred and clinical certification - such as CCRP, CRP, SoCRA nice to have. Real experience with FDA regulations and GCP, related to medical device trial. Background managing trials, people, and training and mentoring staff. 2 to 5 years working in trials related to medical device. Able to write protocols, multitask, work in a team or solo. Background working with doctors and staff. Best if candidate understands the process of medical device development. 30% travel. Need to be living in MA, to be close to sites in question. Type of personality that will fit into very active, energetic group. Must be able to interact with people at a high level and be the face of the company. 30% travel.
Job ID: 2601N
Position: 2601N Medical Physicist - Radiation Physics Therapy Illinois
Location: Chicago area, IL
Description: Hospital system in greater Chicago, IL requires a medical physicist is to guide the radiation oncologist(s), and related specialists in factors involving radiation physics therapy. This physicist, (advised by a Radiation Safety Committee) will be partially responsible for managing the radiation safety program in the Radiation Oncology department. REQUIREMENTS: Ph.D. in Medical Physics or equivalent required. Plus a Medical Physics Residency program, if required for ABR Certification. Eligible to IL state licensure IEMA (Illinois Emergency Management Agency). 3 years' radiation therapy physics experience preferred. Cognizant of High Dose Radiation Policies and Procedures. Able to plan HDR treatments. Knowledgeable in and capable of planning Intensity-modulated radiation therapy (IMRT),Stereotactic radiosurgery (SRS), and Stereotactic body radiotherapy (SBRT) treatments, including arcs, required. Must be legally allowed to work in the State of Illinois.
Job ID: 2585N
Position: 2585N Cerner Patient Accounting/Billing Analyst West Virginia
Location: Huntington, WV
Description: West Virginia client requires an experienced contractor/ consultant to convert their revenue systems to Cerner. Should have at least 2 full implementations of Cerner Patient Accounting. 18 month contract position. RESPONSIBILITIES: Lead Patient Accounting Analyst role to assist in System Implementation / Testing / Validation and Go-Live. Cerner Patient Accounting customization and setup, maintenance, support/troubleshooting. Lead resource on downstream effect on the claim data from both technical and functional perspective for PA components Works hand in hand with HIS through Issue Identification/Troubleshooting/Optimization of Patient Financial Services Billing Electronic bills are submitted to a clearing house via the 837 file Collections Denial Management Cash Posting REQUIREMENTS: BS. Need at least 2 full implementations of Cerner Patient Accounting Must work On-Site.
Job ID: 2451
Position: 2451 Sr. CRO Toxicologist Study Director Montreal
Location: Montreal, QC
Description: Montreal, Quebec preclinical testing laboratory seeks a Toxicology Study Director to be responsible for toxicological (GLP) investigation of pharmaceuticals. ROLE AND RESPONSIBILITIES: Designing protocols and programs. Overseeing all technical and scientific activities and in-life monitoring. Communicating with sponsors. Writing reports and evaluating data.Serving as the scientific representative on corporate committees. Attending scientific meetings. Training of junior technical and scientific personnel. Carry out R&D in line with company objectives. REQUIREMENTS: B.Sc. (min) plus 5 years as a Toxicology Study Director in the CRO, biotechnology, or pharmaceutical industry. Experience conducting toxicology testing. Experience with safety studies of biologics and drugs. Excellent organizational and report writing skills, working knowledge of GLP. Please note that this is GLP, not GMP or GCP. Hands-on, able to deal with the animal experimentation side of testing. Experience leading others of great interest. French / English bilingual nice to have.