Chair, Department of Pediatrics, Rowan-Virtua SOM Rowan UniversityChair, Department of Pediatrics, Rowan-Virtua SOMNJ$200,000–$250,000 / yearThe individual must have prior experience in management roles, academic and professional experience necessary to qualify at the rank of Professor (preferred) or Associate Professor and be able to demonstrate and provide examples of leadership (i.e. previous departmental leadership positions, involvement in regional/national organizations etc.), teambuilding (i.e. previous successes, experience, interpersonal skills), academic strength (i.e. teaching experience, research experience, publications), clinical strength (peer recognition, reputation, patient satisfaction) and management strength (coaching, type and quality of management experience, advanced degree with experience). Responsible for the clinical education and training of students, residents and fellows; providing guidance to faculty and staff serving as clinician educators, course directors and program coordinators for training in geriatric education.
Research Associate (Non-Tenure Track) Rutgers The State University of New JerseyResearch Associate (Non-Tenure Track)Camden, NJUnder Policy 100.3.1 Immunization Policy for Covered Individuals, if employment will commence during Flu Season, Rutgers University may require certain prospective employees to provide proof that they are vaccinated against Seasonal Influenza for the current Flu Season, unless the University has granted the individual a medical or religious exemption. Ranked #46 in U.S. News & World Report's list of Best Public Colleges and Universities, Rutgers University-Camden is a diverse, research-intensive campus of approximately 6,100 students at the undergraduate, graduate, and doctoral levels and 1,100 faculty and staff members.
Psychedelic Therapist Facilitator, PRN (Contract) CenExelPsychedelic Therapist Facilitator, PRN (Contract)Marlton, New JerseyPossesses the experience and wisdom to understand the degree of activity of the role and generally not act as an “inactive sitter” or “overactive guide” but can act in either of these roles as required. Therapist/Facilitator will report any potential contraindications for participation in the study that may arise during therapist visits that would need to be communicated to the Principal Investigator to determine the participants continued eligibility.
Clinical Research Associate 1 Allen SpoldenClinical Research Associate 1Philadelphia, PennsylvaniaConduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
Clinical Research Coordinator Sr. CenExelClinical Research Coordinator Sr.Marlton, New JerseyIndependently responsible for coordinating all aspects of multiple and/or complex clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies. Works collaboratively with internal departments, sponsors and investigators to ensure protocols are understood and assists in training staff members.
Clinical Research Associate II Allen SpoldenClinical Research Associate IIPhiladelphia, PennsylvaniaConduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
Clinical Research Coordinator II Cooper University Health CareClinical Research Coordinator IICamden, NJOur extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. Assists the Principal Investigator and other members of the research team with preparation of IRB protocols, consent forms, and development of study budget.
Research Assistant PRN Cooper University Health CareResearch Assistant PRNCamden, NJThe ideal candidate will have prior experience in a biological research laboratory and experience working with rodents in a wet lab setting Ability to analyze research results using statistical software Demonstrated computer skills and proficiency with MS Office suite or similar spreadsheet, database, word processing and presentation software Ability to work in a collaborative, team-oriented environment, and strong communication skills are required Ability to work early mornings, evenings, and weekends to administer study protocols, as necessary. Processing the clinical samples such as embedding, section and staining using HE or IHC as needed Maintaining a mouse colony, contributing experimentally to ongoing research projects and overseeing general laboratory operations and laboratory supplies Training residents or fellows under supervision in research methods and procedures as needed Performing other duties as assigned.
Sponsored Programs Administrator Cooper University Health CareSponsored Programs AdministratorCamden, NJThis role requires coordination with principal investigators (PIs), department administration, program staff, compliance office, legal, and grants accounting to ensure compliance, financial accuracy, and oversight of all aspects of sponsored projects administration, along with data analytics for the proposal and awards portfolio under management. The Sponsored Projects Administrator will manage the full grant lifecycle - from supporting all aspects of proposal preparation (pre-award) to overseeing award set-up, reporting, and closeout (post-award).
Research Assistant Part Time Cooper University Health CareResearch Assistant Part TimeCamden, NJWorking knowledge of general principles in genetics and molecular biology, as well as accurate and timely record keeping, careful organization, and demonstrated interest in working in a laboratory setting is needed to excel in this role• Have prior experience in a biological research laboratory and experience working with rodents in a wet lab setting • Ability to analyze research results using statistical software• Demonstrated computer skills and proficiency with MS Office suite or similar spreadsheet, database, word processing and presentation software• Ability to work in a collaborative, team-oriented environment, and strong communication skills are required• Ability to work early mornings, evenings, and weekends to administer study protocols, as necessary. Assists the Principal Investigator and other members of the research team with preparation of IRB protocols, consent forms, continuing reviews, amendments, and maintenance of study budget.
Vascular Specialist- HUP Vascular Lab- Full-Time, Day Shift Penn MedicineVascular Specialist- HUP Vascular Lab- Full-Time, Day ShiftPhiladelphia, PAClinical•Performs all aspects and modes vascular laboratory testing, including arterial, venous, cerebrovascular and visceral according to established procedures and protocols•Performs patient assessment, obtains pertinent history, review orders to insure correct and accurate testing is performed•Prepares preliminary report of test results and communicates results to the referring health care provider•Maintain accurate and complete patient records including worksheets, photographs, videotapes, paper and computerized reports•Assist technical director in compilation of quality assurance and improvement programs.•Assist in preparing and maintaining compliance with regulatory agencies and in the ICAVL accreditation process•Assist in the orientation of new employees•Assist in the proper maintenance and use of equipment•Assist in patient and staff education regarding vascular disease and technologyClerical/financial•Perform clinical work flow duties in Penn Chart. Penn Medicine is dedicated to our tripartite mission of providing the highest level of care to patients, conducting innovative research, and educating future leaders in the field of medicine.
Research Assistant PRN Cooper University HospitalResearch Assistant PRNCamden, New JerseyPer diemWorking knowledge of general principles in genetics and molecular biology, as well as accurate and timely record keeping, impeccable organization, and demonstrated interest in working in a laboratory setting is needed to excel in this role. The successful candidate must be proficient in mouse husbandry, PCR-based genotyping, cell culture, flow cytometry, as well as DNA, RNA, and protein isolation and detection techniques.
Research Assistant-Part Time Cooper University HospitalResearch Assistant-Part TimeCamden, New JerseyPart timeWorking knowledge of general principles in genetics and molecular biology, as well as accurate and timely record keeping, careful organization, and demonstrated interest in working in a laboratory setting is needed to excel in this role. Best Regards , Short Description: Assists the Principal Investigator and other members of the research team with preparation of IRB protocols, consent forms, continuing reviews, amendments, and maintenance of study budget.
Oncology Research Pre-Post Award Associate Cooper University HospitalOncology Research Pre-Post Award AssociateCamden, New JerseyFull timeThe role of the Oncology Research Pre-Post Award Associate is to develop the clinical trial agreements, budgets and coverage analyses for industry sponsored clinical trials to bring new clinical trials to our patients and complete research billing review in Epic and facilitate research invoicing for industry sponsored and federally-funded clinical trials and work with the Clinical Research Coordinators and grants management colleagues to support accurate billing and invoicing. Collaborate with clinical research coordinators to completed Research Billing Review in Epic to review accounts and identifies charges billable either to insurance or the clinical research study.
NewMedical Value Access Liaison - Pittsburgh/Ohio Amgen IncMedical Value Access Liaison - Pittsburgh/OhioPhiladelphia, PAIdentify, develop, and maintain collaborative relationships with current and future Payer, Policy, IDN, and Health Economic and Outcomes Research opinion leaders through identifying speaker opportunities and concepts and letters of intent for investigator supported economics, humanistic outcome, and non-registration clinical studies to support Amgen's product messages within scope. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
NewClinical Research Coordinator II Cooper University HospitalClinical Research Coordinator IICamden, New JerseyFull timeOur extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. Short Description: Assists the Principal Investigator and other members of the research team with preparation of IRB protocols, consent forms, and development of study budget.
Sponsored Programs Administrator Cooper University HospitalSponsored Programs AdministratorCamden, New JerseyFull timeThis role requires coordination with principal investigators (PIs), department administration, program staff, compliance office, legal, and grants accounting to ensure compliance, financial accuracy, and oversight of all aspects of sponsored projects administration, along with data analytics for the proposal and awards portfolio under management. Short Description: The Sponsored Projects Administrator will manage the full grant lifecycle — from supporting all aspects of proposal preparation (pre-award) to overseeing award set-up, reporting, and closeout (post-award).
Contract Reviewer Cooper University HospitalContract ReviewerCamden, NJReviews IRB submissions for funded studies and provides financial disclosure clearance for key study personnel and reconciles whether Legal or the Privacy Officer need to provide Material Transfer. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols.
Vascular Technician - Per Diem (PRN) - HUP Penn MedicineVascular Technician - Per Diem (PRN) - HUPPhiladelphia, PASummary: Clinical•Performs all aspects and modes vascular laboratory testing, including arterial, venous, cerebrovascular and visceral according to established procedures and protocols•Performs patient assessment, obtains pertinent history, review orders to insure correct and accurate testing is performed•Prepares preliminary report of test results and communicates results to the referring health care provider•Maintain accurate and complete patient records including worksheets, photographs, videotapes, paper and computerized reports•Assist technical director in compilation of quality assurance and improvement programs.•Assist in preparing and maintaining compliance with regulatory agencies and in the ICAVL accreditation process•Assist in the orientation of new employees•Assist in the proper maintenance and use of equipment•Assist in patient and staff education regarding vascular disease and technologyClerical/financial•Perform clinical work flow duties in Penn Chart. Education Specialization: Equivalent Experience: •And Graduate of accredited ultrasound technology program •Or 1+ years Clinical experience in performing vascular lab testing •And Must possess skills in performing Vascular Lab testing.
Research Pharmacy Technician--HUP--Investigational Drug Pharmacy Penn MedicineResearch Pharmacy Technician--HUP--Investigational Drug PharmacyPhiladelphia, PAUnder the supervision of the IDS pharmacist, the role is responsible for providing patient care services to patients enrolled in clinical trials, oversee investigational drug inventory and storage, including record keeping and drug accountability, ordering and receiving products, tracking expiration dates, processing drug returns and destruction after study closure. Ensures proper distribution/delivery of investigational pharmaceutical and supply shipment, provide support for drug procurement staff including unpacking stock, documenting receipt, and proper storage.