Anticipate and identify site issues that could affect timelines and develop alternative solutions.Ensure clinical Ensures timely payment execution for the assigned sites study(s) according to the clinical study agreements per local requirements.Ensure adherence to federal regulations and applicable local regulations, Good Clinical AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical tactical success throughout the study planning, execution, and closeout phases leading to World Class clinical
SUMMARY Great opporitny to join a global Medical Device company who are looking to bring onboard a Clinical Join a small clinical team with management based in the UK. REQUIREMENTS To be successful in this role you will need to have prior clinical research experience either with a healthcare company, Clinical Research Organisation (CRO) or hospital health care provider and a passion for innovation. Ability to travel up to 50 , depending on the stage and needs of the clinical
ICON plc is a world leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical As a Clinical Research Associate at ICON, you'll work within a large scale, fast paced environment alongside team of highly qualified CRAs to identify, select, initiate and close out investigational sites for clinical ourselves on our amazing company culture, where we work as one team to achieve industry leading results. Clinical
lead, plan, organize and oversee all activities related to the execution of complex and international clinical Bachelor's degree, or international equivalent from an accredited college or university, preferably in a clinical biological or science related field. Experience in the clinical research industry. Min 2. years of clinical project management experience, preferably in a pharmaceutical company CRO in complex and or international clinical trials and or programs, with specific experience managing Analgesic studies.
Service Provider to a leading Medical Device Company Parexel FSP is currently looking for a Senior Clinical This position provides oversight of clinical research sites compliance with ICH Good Clinical Practices GCP), governing SOPs (standard operating procedures) and clinical study protocols Main responsibilities Serves as the primary monitoring point of contact for assigned clinical research sites. research sites with designated program SOPs, Client expectations, clinical study protocols and GCPs
IQVIA is seeking a proactive and highly a motivated. Nurse Program Co Ordinator. to provide program administration This includes all program contacts from an operational and clinical perspective, and. frequent contact ensure satisfaction and quality program delivery. Adverse Event reporting management, quality checks, nurse operations by performing all the responsibilities and duties outlined in this Job Description.As a Nurse
Clinical Trial Liaison. Rare Disease. Nephrology. Australia. Business Unit. Clinical Operations. an opportunity for you to support an exciting biopharmaceutical company and its ongoing and future clinical trials as a Clinical Trial Liaison (CTL) in rare disease. nephrology space.The CTL will represent the Reporting into the US Sr Director Clinical Compliance. . as required. Support relevant education at Site Investigator Meetings (SIMs) in line with clinical
Communication and consultation with facility medics associated with clinical governance.Support with What you need to bring. What you need to bring. Qualifications in Occupational Health Nurse Registered Nurse.Experience in coordination and delivery of occupational health services (advisor or
needed for medical activities including KOL engagement, executing medical plans and tactics and support clinical key accounts. Through these relationships and insights, direct and manage new medical, scientific and clinical reimbursement activities. Identify and engage opportunities for data generation including RWE, IIS and clinical degree (MD, PhD), Pharmacy degree or Master Degree (equivalent) in. Medical Field (Pharmacy, Nursing). Clinical Field Medical within pharmaceutical experience. Strong track record in KOL engagement. Experience in clinical
Clinical Research Associate (CRA). Description of Roles and Responsibilities. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility Performs clinical study site management monitoring activities in compliance with ICH GCP, Sponsor Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP ICH & country clinical research law & guidelines
New Laboratory. Clinical Drug Development. New Role. The company. Our client, a Melbourne based biotechnology The company now seeks to build on its capabilities to continue their transition from R&D to clinical The QC lab will support the manufacture of our client's drug products for clinical trials. variety of opportunities in the area of Sales & Marketing, Management, Medical, Regulatory Affairs, Clinical
In this position, you will perform QA review of batch documentation for R&D pre clinical and clinical product batch release to meet the R&D product release timelines for use in clinical studies sponsored
Clinical Midwife Educator x 2 ongoing permanent positions 0.74 1.0EFT availableUnique opportunity for a motivated, progressive midwife to undertake a permanent Clinical Midwife Educator (CME) positionExperience an Educator role, supporting Nursing and Midwifery staff across Monash Women's predominately at Clayton Midwife Educator position. care and sound clinical skillsAbility to work effectively with a multi disciplinary teamAbility to show
The ClinicalNurse Consultant. Pain Management provides clinical consultancy care to and supports the as provide leadership in evidence based pain management through teaching and provision of advice to clinical experience in an acute care settingDemonstrated experience in the development, delivery and evaluation of clinical
same ambition of our hospital to provide the highest quality care for our patients.As a registered Nurse you will have AHPRA registration, a, possess extensive clinical skills and experience within the medical field (preferably 2 years clinical nursing experience.
progressive environment, then come and join a dedicated team in a very rewarding career as a Registered Nurse you will have. Bachelor of nursing. Current AHPRA registration. Demonstrated competence in a senior clinical position. Advanced clinical skills. Excellent interpersonal, communication and networking skills. Demonstrated enquiries or to request a copy of the Position Descriptions, please contact Claire McGregor, Director of Clinical
Experienced Allied Health Professional is sought to be an extraordinary Clinical Lead for a genuinely to make this role your ownAn experienced Allied Health Professional is sought to be an extraordinary Clinical
Reporting to the Director of Clinical Services, the Nurse Unit Manager (NUM) of Aged Care is considered To be eligible for this role you will hold current registration as a Registered Nurse. Midwife with You will be able to demonstrate extensive clinical skills and knowledge of contemporary nursing practice
The role. GP Synergy is seeking a committed and experienced senior medical educator who A Senior Medical Educator takes a leadership role in projects, programs and within the medical education essential applicants meet the following criteria together with the requirements as outlined in the Medical Educator Unrestricted motor vehicle licence (own transport is preferred) Experience as a GP Supervisor and or clinical
Perioperative Services Manager works closely with the Executive team and in particular the Director Clinical quality patient care.To be eligible for this role you will hold current registration as a Registered Nurse You will be able to demonstrate extensive clinical skills and knowledge of contemporary perioperative
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