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- ...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 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
- ...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 workInterim roleLocal areaImmediate 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$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$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- ...clinical technology Experienced support staff, including dedicated medical assistants providing scribing support User-friendly EMA electronic medical record system Comprehensive operational support covering billing, marketing, HR, IT, compliance and practice management...SuggestedWork experience placementLive inWork visaRelocation package
MyDermRecruiter
Austin, MN11 days ago $72.4k - $108.6k
...preparing DCSA Forms 147 and coordination with DCSA/FSO for approval Support Security UL 2050 program and vendor with project status, EMA compliance, site PO’s, and invoices for integrator vendor Support Business resiliency and contingency planning for the Crisis...SuggestedContract workWork at officeRemote workRelocationShift work- ...generated content: Evaluate marketing materials, claims, and references for medical accuracy, clinical soundness, and compliance with FDA/EMA regulations. Collaborate with design and medical teams: Work alongside design and medical copywriting teams to ensure generated...Suggested
$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...SuggestedTemporary workLocal areaRemote workWeekend work$110k - $165k
...interacting with site personnel, inspectors, and internal and external vendors required. Experience leading or directly supporting FDA, EMA, and/or international regulatory inspections required. Ideal: Experience and/or full knowledge of manufacturing operations,...SuggestedFull timeContract workRelocation packageFlexible hours$120k - $135k
...to hear from you. 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. Additional Information Tasks, duties, and...SuggestedRemote jobWork at officeWorldwide$110k - $165k
...preparation, mock inspections, and remediation efforts. Ensure microbiology programs remain inspection-ready and compliant with FDA, EMA, and global regulatory expectations. Build, mentor, and develop a high-performing microbiology and sterility assurance...Full timeContract workRelocation packageFlexible hours- ...patients per day Modern office equipped with advanced technology and the resources needed to provide comprehensive dermatologic care EMA / EMR platform for efficient, intuitive documentation Experienced medical assistants and dedicated scribes providing strong...Full timeWork experience placementWork at officeImmediate startWork visaRelocation packageFlexible hours
myDermRecruiter
Minneapolis, MN4 days ago - ...assessments (FMEA, impact assessments), SOPs, deviation investigations, and CAPAs. Ability to support regulatory inspections and audits (FDA, EMA, internal, or client audits). Strong technical writing skills with attention to detail and data integrity. Proficiency with common...
Katalyst CRO
Minneapolis, MN2 days ago $233k - $315k
...supporting labeling, CCDS development, and post marketing safety activities. Experience with global filings and interactions with FDA/EMA and other health authorities. Strong clinical judgment and patient safety mindset. Ability to translate complex safety data...Temporary workRemote workTravere Therapeutics
Minneapolis, MN1 day ago
