Clinical QA Specialist - Regulatory Documents
Integrated Resources Inc.
A leading staffing firm seeks a Clinical Data Quality Reviewer to ensure accuracy in clinical and regulatory documents. Candidates should have at least 3 years of relevant experience in clinical settings, focusing on data quality review and medical writing. Strong analytical, communication, and detail-oriented skills are essential for this role, offering an engaging environment within the healthcare industry. #J-18808-Ljbffr Integrated Resources Inc.
$35 - $40 per hour
Piper Companies is currently looking for an experienced QA Clinical Supplies Specialist in Lansdale, PA to work for an innovative and growing pharmaceutical... ..., storage, etc. · Review of Electronic records for regulatory submissions (IND or CTA) · Areas of focus will include...Regulatory$40 - $45 per hour
...seeking a Quality Assurance Specialist for an opportunity in Audubon... ...where applicable approve GMP documents (such as Change Controls, Effectiveness... ...preferred Knowledge of cGMP, regulatory requirements, and industry... ...#LI-KP1#LI-ONSITE Keywords : QA, quality assurance, QMS,...DocumentRegulatoryPermanent employmentContract work- ...Clinical Operations SpecialistICON is a global healthcare intelligence and clinical research... ...trials, ensuring compliance with regulatory requirements, and contribute to the advancement... ...and submission of regulatory documents, including clinical trial applications,...DocumentRegulatoryLocal area
$33 - $43 per hour
...seeking a Quality Assurance Specialist to join a cutting-edge company... ...Point, Pennsylvania . The Clinical Supplies Quality Specialist... ...distribution activities and associated regulatory submissions for... ...Specialist, Quality Specialist, document review, rights and well-...DocumentRegulatoryLong term contractFull time- ...SEI is seeking a Compliance Officer to support ongoing regulatory activities for registered investment funds with a strong emphasis on... ...members, you will contribute to efficient compliance workflows, document reviews, and due diligence support while maintaining audit-...DocumentRegulatory
- ...with 3-5 years of experience and preferred pharmaceutical expertise. The role involves preparing local product documents and ensuring compliance with regulatory standards. The ideal candidate will communicate effectively, prioritize tasks, and support various labeling...DocumentRegulatoryLocal area
- Tower Health is seeking a qualified coordinator for clinical research studies. This role involves facilitating and overseeing research... ...and outpatient settings, with a strong emphasis on regulatory document processing and interactions with sponsors. Qualifications include...DocumentRegulatory
- ...educating patients and families on hearing loss prevention, documenting clinical findings, collaborating with other healthcare professionals... ...maintaining accurate patient records in accordance with regulatory and ethical standards. The Audiologist will also contribute...DocumentRegulatoryFull timePart timePrivate practice
- ...Description Quality Assurance Specialist Full-Time | Onsite |... ...Review DHR and supporting documentation to ensure compliance with product... .... Provide final QA disposition and release of finished... ..., customer audits, and regulatory inspections. Develop and...DocumentRegulatoryFull timeWork at office
- ...involves coordinating with stakeholders, ensuring compliance with regulatory timelines, and supporting large-scale projects. Candidates... ...specifically in labeling, regulatory aspects, or packaging. Relevant document management tool experience is also required. This is a 12-...DocumentRegulatoryContract work
- An innovative pharmaceutical manufacturer in Lansdale, PA, is seeking a QA Clinical Supplies Specialist. This role involves electronic batch record reviews, ensuring compliance with regulations, and requires 5+ years of experience in quality assurance within biologics or...
$80k - $100k
...seeking compassionate and dedicated Licensed Clinical Social Workers (LCSW) to join our... ...Ensure meticulous record-keeping by documenting sessions and progress consistently, adhering... ...latest research, best practices, and regulatory changes in the field of social work. \n...DocumentRegulatoryRemote jobFull time$239.9k - $399.8k
...Job SummaryThe medical director provides Clinical Development leadership and expertise on... ...works closely with other functions such as regulatory affairs, pharmacovigilance,... ...maintenance of clinical trial and regulatory documents, in collaboration with Clinical Scientist...DocumentRegulatoryPermanent employmentFull timeInternshipH1bLocal areaVisa sponsorshipWork visaRelocation package2 days per week- ...practicesAssist the People & Culture team with workforce-related regulatory filings and required employee noticesCollaborate with client... ...and pre-litigation disputes, including fact development, document preservation and production, and coordination with witnesses and...DocumentRegulatoryFull timeWork at officeFlexible hours
- ...specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and... .../QC on clinical components of assigned documents (eg, clinical study reports,... ...brochures, manuscripts, summary documents, regulatory responses, etc.). • Formally documents findings...DocumentRegulatoryImmediate start
- ...provide strategic legal leadership and counsel on a wide range of regulatory, commercial, litigation, policy, and stakeholder-related... ...The role also involves developing and reviewing various legal documents, representing the company in legal proceedings, and engaging with...DocumentRegulatory
- ...specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.... ..., pharmacology and bio therapeutic summaries, regulatory responses, internal and external risk/benefit briefing documents, for one or more assigned products. High quality...DocumentRegulatoryContract work
- ...support our client's legal & compliance efforts by preparing documents and filings, provide support for activities related to drafting... ...-filing, and have a thorough knowledge of legal procedure and regulatory/compliance matters. Essential Duties: Assist attorneys in the...DocumentRegulatoryContract workWork at officeRemote work
- ...researchers and educators to transform clinical insights into tangible solutions. Our solutions... ...(version control, tool chains, documentation tools) and quality system.· Actively contribute... ...assist projects lead in the writing of regulatory documents required for product/software...DocumentRegulatoryFull time
$28.5 per hour
...Clinical Operations Specialist Rate: $28.50/HR Location: 770 Sumneytown Pike, West Point, PA 19486 Qualifications Education Requirements... ...ship of clinical drug shipments Understand and apply regulatory/ compliance requirements relative to the role Receive,...RegulatoryWork at office- ...seeking an experienced and motivated Safety Specialist to support heavy civil and highway... ...potential incidents and health hazards, documenting through safety software and... ...operations team and communicating with regulatory authorities · Develops, coordinates...DocumentRegulatoryFull timeWork at officeLocal area
$87.2k - $145.3k
...visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on... ...-up phase.Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF...DocumentRegulatoryFull timePart timeLocal areaImmediate startWorldwide$42k - $50k
...position supports agency attorneys and administrators with the regulatory enforcement of peace officers and private security standards.... ...ideal candidate manages legal files, formats state compliance documents, and interfaces professionally with Oklahoma state agencies, and...DocumentRegulatoryFull timePart timeWork at office- ...Clinical Scientist A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states... ...integrity oversight • Safety review and communication • Regulatory document, study report and publication preparation and review •...DocumentRegulatory
- ...funds, interval/closed end funds and ETFs. This role focuses on regulatory filings, board reporting, adviser oversight, and compliance... ...recurring compliance activities, including monitoring tasks, documentation updates, workflow tracking, deadline management, and...DocumentRegulatoryWork experience placementInternshipWork at officeImmediate startFlexible hours
- ...Responsibilities:• Uphold Viant Values and comply with all safety, regulatory, and quality requirements, policies, and procedures.• Provide... ...in management of production schedules, reading technical documents and blueprints preferred. Lean Six/Sigma Green/Black Belt or Lean...DocumentRegulatoryFlexible hoursShift work
- ...Market Coordinator” role on behalf of WSR Regulatory Strategy functions at Country Offices... ..., specifications and/or supportive documentation is available for plants/artwork centers... ...ALIM Market Implementation Specialists Regulatory Strategists Global Services...DocumentRegulatoryContract workWork experience placementLocal area
- ...with Internal & External Audit partnersFacilitation and project management of SOX ITGC document requests; rationalize and challenge document requests according to precedents and regulatory requirementsManage document and project related request tracking and follow up with...DocumentRegulatory
$295.9k
...Power for PurposeThis position is for a Clinical Development Medical Executive Director supporting... ...the GDPL Accountable for integrating regulatory, statistical and other internal and... ...of clinical trial and regulatory documents, in collaboration with Clinical Scientist...DocumentRegulatoryPermanent employmentFull timeH1bLocal areaVisa sponsorshipWork visaRelocation package2 days per week$274.5k
...individual contributor position will be responsible for supporting clinical trial(s) and lead subteams in clinical development. The... ...to development and maintenance of clinical trial and regulatory documents, in collaboration with Clinical Scientist and the cross-functional...DocumentRegulatoryPermanent employmentFull timeH1bLocal areaVisa sponsorshipWork visaRelocation package2 days per week
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