Clinical Research Manager
$120k - $130kSocket
NS Pharma is a highly focused, research-driven biopharmaceutical company working in rare diseases. We're exploring the potential of cutting-edge science as a subsidiary of Nippon Shinyaku Co., Ltd. In Japan. Job Summary This is an individual contributor role that supports the execution of assigned global clinical studies with adherence to all relevant regulations including FDA, ICH, local Regulatory requirements and NS Pharma standard operating procedures. This is a hybrid position that requires to travel to the Paramus, NJ office at least twice a week. Essential Duties and Responsibilities Assist in the planning, implementation and management of assigned regional or global clinical studies. Facilitate CRO./vendor selection process. Maintain oversight of assigned study vendors (e.g. central labs). Perform assigned activities in the selection of clinical sites. Attend and participate in site visits including pre-study assessments, site initiations, co-monitoring and ad-hoc site visits based on the study’s needs. Review site visit reports, identify issues and ensure issues are resolved. Oversight of patient recruitment and development of recruitment strategies and plans. Track, review, report and present study metrics including enrollment, protocol deviations, issues, risks, data resolution, and other study related metrics. Support the development of study related documentation (protocol, ICF, CRF, operations manuals, etc.); facilitate internal review of these documents as assigned. Tracking of clinical data, regulatory documents, and patient Assure compliance of investigational sites with SOPs, FDA regulations, ICH guidelines and protocol requirements. Facilitate internal review of clinical trial agreements and ancillary agreements.. Implement and maintain study-specific training program. TMF oversight review during study conduct and TMF management during study closeout. Support creating and maintaining clinical SOPs as part of global QMS. Perform administrative tasks (e.g. setting-up and facilitating meetings, clinical registrations). Perform other tasks and functions as needed. Qualifications Thorough understanding of clinical operations including strong knowledge on essential documents as related to the planning, launching, and closing clinical studies. Must be able to manage and coordinate with the Clinical Lead(s), Study Manager(s), Operations Program Lead and study team members at Headquarters Office in Japan to achieve study objectives and team goals. Must have the ability to identify and manage/solve study team’s performance issues if they arise with minimal supervision. Must have demonstrated ability to support the development and management of various aspects of the study operational plans from start-up to close-out. Must be able to work effectively in a multi-cultural, global team environment and support drug development collaboration with global project teams, Headquarters Office in Japan, external partners and vendors. Ability to handle multiple tasks and prioritize. Strong organizational, attention to details, communication and presentation skills. Team player, flexible, ability to adapt to change. Ability to interact with Investigators in-person to discuss protocol requirements and study drug. Ability to travel 15-25% monthly within the US and/or outside of US. Education and/or Experience Bachelor’s Degree in sciences (highly preferred) or related field with a minimum of 3 to 5 years of pharmaceuticals/biotech experience Minimum of 3 to 5 years drug development experience in the pharmaceutical industry/CRO or commensurate clinical/medical research experience with emphasis on Phase II-IV clinical trials. Program and project management experience preferred. Global clinical trial experience is also preferred. Rare Disease experience highly preferred Compensation And Benefits: NS Pharma employees embrace our Mission to Help People Lead Healthier Happier Lives. We pride ourselves in offering employees and their families a robust Compensation and Benefits package designed to meet their needs, on and off the job. The annualized target salary range for this role is $120,000 to $130,000; actual salaries will vary and may be above or below this range depending on several factors, including experience, education, training, location, and merit. Other benefits include: Medical, Dental & Vision Insurance, Basic and Voluntary Life and AD&D Insurance, Short- and Long-Term Disability Insurance, Flexible Spending Account, Health Savings Account, and Employee Assistance Programs Discretionary Bonus Programs and Long-term Incentive Plan Retirement Savings 401k with company match Generous Paid Time Off, Sick Time & Paid Holidays Career Development, Progression and Training Flexible Work Arrangement Programs Paid Parental Leave Year-End Paid Holiday Shutdown NS Pharma is an EEO employer. #J-18808-Ljbffr
$210k - $245k
...NS Pharma is a highly focused, research‑driven biopharmaceutical company working in rare diseases. We're exploring the potential... ..., Ltd. in Japan. Summary Accountable for the oversight, management, and execution clinical studies (feasibility, country and site selection,...SuggestedTemporary workFlexible hours$50.18 - $62.73 per hour
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$110.2k - $176.4k
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$210k
...engaged, and passionate veterinary leader with several years of clinical experience to lead our team of emergency and specialty... ...BluePearl. ~ BluePearl University – our own built-in learning management system. ~ RECOVER CPR certifications – FREE. ~ BluePearl Pet...Full timeTemporary workRelocation package- ...Global Development Lead (GDL) represents Clinical on the Global Medicine Team and is the... ...MD or DO. ~8+ years relevant clinical research and development experience (academia and... ...regulation, ICH/GCP, and adverse event management. Preferred/Required Skills & Competencies...Worldwide2 days per week
- ...Hospital in Northern, New Jersey is seeking Clinical Data Coordinators for their Outpatient Clinical Research Operation. Company Six-time recipient of "... ...CCRP) certification and/or Certified Clinical Data Manager (CCDM) preferred keywords: clinical data...Temporary work
- ...Clinical Program Manager – NJ USA Delivery experience of large programs having multiple projects Can make relationship and win customer trust Functional knowledge of various global drug development clinical testing business. Should be able to guide POs Able...
$150k - $175k
...Veterinary Medical Director to lead its clinical team while continuing to practice high-quality... ...Senior pet care Chronic disease management Urgent medical cases The caseload... ...resources Participation in clinical research and studies Career advancement pathways...Full timePart timeLocal areaMonday to FridayFlexible hoursAfternoon shift$100k
...Research & Development ManagerSouth Hackensack, New Jersey, United StatesAbout the JobWe are seeking a qualified R&D Manager with proven expertise in the Korean Beauty (K-Beauty) industry to join our dynamic team. The ideal candidate will possess strong bilingual capabilities...Contract workH1b- ...executing them on time and within budget• Overall coordination and management of clinical trials from startup to closeout• Liaise with other... ...of overall clinical drug development and general clinical research operations in Big Pharma.Ability to manage multiple projects...Work at officeImmediate start
$150k - $220k
...Associate Director, Clinical Pharmacology Job Locations US-NJ-Paramus ID 2026-2004 Category Clinical... ...for one or more early and late-stage clinical and lifecycle management projects/programs Provide support in the designing and interpreting...Full time$60k - $75k
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$90k - $100k
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$112.29k - $140.37k
...operational accountability for a specified shift. On a 24/7 basis, this individual shall have primary responsibility for human resource management, operational management, in the absence of the unit manager, as well as acting on behalf of the Hospital President in the absence...Full timeTemporary workPart timeLocal areaFlexible hoursShift workNight shiftWeekend work$150k - $175k
...and the care team Opportunities to participate in a robust Clinical Studies program Discover Additional Benefits Benefits | VCA... ...and qualifications required of associates assigned to this job. Management reserves the right to revise the job description or require...Full timeRelocation packageFlexible hoursAfternoon shift
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