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- ...the role. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll...SuggestedContract workFlexible hours
- ...required. Other duties as assigned REQUIRED EXPERIENCE/SKILLS: ~ Medical Terminology ~ EMR knowledge (Helpful if familiar with EMA/ModMed and/or NexTech) ~2 years front office experience required ~ Excellent computer and phone skills are required for this role...SuggestedWork at officeShift work
- ...the role. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll...SuggestedContract workFlexible hours
- ...Finance on budgeting, forecasting, cost optimization Compliance & Quality Ensure all clinical supply activities comply with GxP, ICH, FDA, EMA, and global regulatory requirements Lead inspection readiness activities for global filings Team Leadership Build, lead, and mentor a...Suggested
- ...the role. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll...SuggestedContract workInterim roleImmediate startRemote workFlexible hours
- ...the role. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll...SuggestedContract workTemporary workImmediate startFlexible hours
- ...the role. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll...SuggestedContract workInterim roleLocal areaImmediate startRemote workFlexible hours
$120k - $135k
...the role. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll...SuggestedContract workWork at officeImmediate startRemote workWorldwideFlexible hours$79.8k - $139.6k
...the role. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll...SuggestedContract workImmediate startRemote workFlexible hours$95k - $175.7k
...the role. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll...SuggestedContract workRemote workFlexible hours2 days per week3 days per week$80.6k - $145k
...Prior involvement in CAR-T or other cell therapy studies is highly desirable. ~ Strong familiarity with GCP/ICH guidelines , FDA/EMA regulations, and inspection-readiness standards. ~ Experience working in sponsor-dedicated or embedded roles within a CRO is a...SuggestedFull timeContract workWork experience placementWork at officeRemote workFlexible hours$114k - $210.9k
...the role. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll...SuggestedContract workRemote workWork from homeFlexible hours2 days per week3 days per week- ...trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe worlds largest roster of early-phase principal investigators across its Network of clinical trial sites....SuggestedLocal areaWorldwideFlexible hours
START Center for Cancer Research
West Valley, UT13 days ago - ...trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world’s largest roster of early-phase principal investigators across its Network of clinical trial sites....SuggestedLocal areaWorldwideMonday to FridayFlexible hours
START Center for Cancer Research
West Valley, UT11 days ago - ...trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world’s largest roster of early-phase principal investigators across its Network of clinical trial sites....SuggestedLocal areaWorldwideMonday to FridayFlexible hours
$25k
...regulatory information in order to write, edit, and review reports. Work with various governmental and regulatory bodies (e.g., FDA, MHRA, EMA) to ensure compliance and expedite approval of pending registration. Compile all material required for submissions, license renewals,...Temporary workWork experience placement$150k - $195k
...strategy, authoring clinical, regulatory, and scientific documents within the biotechnology or pharmaceutical industry. Knowledge of FDA, EMA, ICH, and other applicable regulatory requirements and guidance related to clinical development and regulatory submissions....Contract workTemporary workWork at officeLocal areaRemote work$189k - $246k
...throughout late-stage development. The role requires extensive experience interacting with global health authorities, including the FDA, EMA, and other regulatory agencies. Responsibilities Regulatory Strategy & Leadership Develop and lead global regulatory strategies for...Temporary workLocal areaRemote workWeekend work- ...trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe worlds largest roster of early-phase principal investigators across its Network of clinical trial sites....Local areaWorldwideMonday to FridayFlexible hours
START Center for Cancer Research
West Valley, UT23 days ago $98.4k - $147.6k
...performing EMI/EMC design work on a missile program Experience with modeling and simulation tools such as Spice, MATLAB, ANSYS HFSS/EMA3D/Maxwell, CST, or other codes Position Benefits As a full-time employee of Northrop Grumman, you are eligible for our robust...Full timeRelocation packageMonday to ThursdayShift work- ...scientific and regulatory information to write, edit, and review reports. Work with governmental and regulatory bodies (e.g., FDA, MHRA, EMA) to ensure compliance and expedite approval. Compile material required for submissions, license renewals, and annual registrations....Work experience placement
University of Utah Health
Salt Lake City, UT3 days ago - ...full time. Primarily General Dermatology with optional Cosmetics including lasers. Very efficient practice that utilizes Scribes and EMA. Physicians only sign their notes at end of day. Base plus production based on collections. Solid benefits including relocation allowance...Permanent employmentFull timeRelocation package
Utah
Salt Lake City, UT3 days ago $25k
...regulatory information in order to write, edit, and review reports. Work with various governmental and regulatory bodies (e.g., FDA , MHRA , EMA ) to ensure compliance and expedite approval of pending registration. Compile all material required for submissions, license renewals...Full timeTemporary workPart timeWork experience placementWork at officeRemote workMonday to FridayShift workUniversity of Utah
Salt Lake City, UT2 days ago
