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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
- ...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
- ...to 25%) 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 take...SuggestedContract workInterim role
- ...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
- ...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
$47k - $79.9k
...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 workLocal areaRemote 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$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$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$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- ...time. Details of the Opportunity: Board Eligible/Board Certified Dermatologist Full time opportunity with Flexible Schedule EMA Enabled Clinic Professional management team to help with clinical operations, marketing, HR, billing, compliance, credentialing,...SuggestedFull timeFlexible hours
Advanced Dermatology and Cosmetic Surgery
Kalamazoo, MI5 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....SuggestedWork at officeLocal areaWorldwideFlexible hoursShift work
START Center for Cancer Research
Grand Rapids, MI12 days ago - ...achieve the highest patient care and customer service standards. Knowledge of ICD-10 and CPT coding Familiarity with the ModMed EMA EMR is strongly preferred. Thorough understanding of HIPAA law Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual...SuggestedWork at office
- ...highest patient care and customer service standards Knowledge of ICD-10 and CPT coding (preferred) Familiarity with the ModMed EMA EMR (preferred) Thorough understanding of HIPAA law Team player Physical Demands Standing or walking for extended periods...SuggestedWork at office
- ...and indirectly manage 100+ employees to achieve on‑time, on‑budget results. Experience in regulatory agency governed industry, FDA or EMA preferred. Prior manufacturing experience in an industrial setting. Proven general leadership and production management experience....Temporary workWork experience placementWork at officeShift work
- ...survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient...Work at officeRemote workWorldwideMonday to FridayFlexible hours
- ...Manufacturing Practices (GMP) and global regulatory requirements. Ensure all project deliverables meet regulatory requirements, including FDA, EMA, and local health authorities. Delivering competency in cost control, including budgeting, forecasting and cost estimation....Local area
- ...Details of the Opportunity: Board Eligible/Board Certified Dermatologist Full time opportunity with Flexible Schedule EMA Enabled Clinic Professional management team to help with clinical operations, marketing, HR, billing, compliance, credentialing, and...Full timeFlexible hours
- ...Experience with CMC regulatory documents (IND/CTAs, NDAs, MAAs, responses, variations, and briefing documents). Knowledge of FDA, EMA and/or ICH guidelines and CMC regulations. Experience in drug development processes and post-approval requirements. Experience in developing...Contract 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. START represents the world’s largest roster of early-phase principal investigators across its Network of clinical trial sites....Work at officeLocal areaWorldwideFlexible hours
- ...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
- ...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....Currently hiringWork at officeLocal areaWorldwideMonday to FridayFlexible hours
- ...medical assistant in Dermatology is REQUIRED and experience in Mohs surgery is an added bonus! Experience with Modernizing Medicine/EMA is preferred. Primary responsibilities will include supporting doctors and patients through a variety of tasks related to patient care...
- ...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....Work at officeLocal areaWorldwideMonday to FridayFlexible hours
- ...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....Currently hiringWork at officeLocal areaWorldwideMonday to FridayFlexible 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...
- ...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 worlds largest roster of early-phase principal investigators across its Network of clinical trial sites....Work at officeLocal areaWorldwideFlexible hours
- ...specialty practice. Familiarity with insurance verification and medical scheduling. Experience using electronic medical records (EMA/Modernizing Medicine preferred). You'll Be Successful Here If You ~ Take ownership without needing constant direction. ~ Stay...Full timeWork at officeMonday to FridayAfternoon shift
