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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
- ...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
- ...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 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 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$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$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$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- ...and problem-solving a must Working knowledge of Good Clinical Practices, Clinical research, Clinical Trial process and related regulatory requirements and terminology. Knowledge of regulatory agency such as the FDA, EMA, PMDA and audit experience a plus....SuggestedInterim roleImmediate start
Katalyst Healthcares and Life Sciences
Omaha, NE1 day ago - ...oversight and appropriate QC for programming deliverables. Provide statistical programming support for regulatory submissions (e.g., FDA, EMA), including electronic submission standards (eCTD). Provides primary programming and QC support for any internally produced...Suggested
Katalyst HealthCares & Life Sciences
Omaha, NE1 day ago - ...Production Planner Group: Filtration Group N. America Division: Engine Mobile Aftermarket Division (EMAM) Location : USA_Kearney, NE EMA Job Family : Planning Job Type : Regular Posted : Jul 1, 2026 Job ID : 65321 Back to Search Results Job Description...Permanent employmentContract workTemporary workFor contractorsWorldwide
Parker Hannifin Corporation
Kearney, NE4 days ago - ...Representative Group: Filtration Group N. America Division: Engine Mobile Aftermarket Division (EMAM) Location : USA_Kearney, NE EMA Job Family : Admin & Support Services Job Type : Regular Posted : Jul 23, 2026 Job ID : 67253 Back to Search Results...Permanent employmentTemporary workFor contractorsWork at officeWorldwide
Parker Hannifin Corporation
Kearney, NE1 day ago $21.74 - $25.57 per hour
...-2nd Shift Group: Filtration Group N. America Division: Engine Mobile Aftermarket Division (EMAM) Location : USA_Kearney, NE EMA Job Family : Manufacturing Job Type : Regular Posted : Jul 1, 2026 Job ID : 64741 Back to Search Results Job Description...Hourly payPermanent employmentTemporary workFor contractorsWork experience placementWorldwideAfternoon shiftParker Hannifin Corporation
Kearney, NE1 day ago$169.22k - $253k
...transfer, and method lifecycle management. ~ Deep knowledge of global regulatory expectations for biologics (ICH Q5, Q6, Q8, Q14; FDA and EMA guidance's). ~ Proven leadership skills and experience managing teams or cross-functional technical groups. ~ Experience with...Contract workTemporary workLocal areaFlexible hoursOtsuka America Pharmaceutical Inc.
Lincoln, NE2 days ago
