Back to Jobs

Director of Clinical reputed company

Remote, USAFull-timePosted 2026-07-28

reputed company reputed company is a premier reputed company firm recognized as one of the tri-states most reputed company-respected reputed company specialty firms. IRI has reputed company its reputed company on excellent service and reputed company since its inception in 1996. Our mission centers on delivering only the best reputed company talent, the first time and every time. We reputed company reputed company resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job reputed company reputed company: Candidates may need to travel to investigator sites Candidates can sit remote but need to be reputed company to travel to Cambridge Local candidates preferred but they can work from home occasionally 1 year assignment to start. Not a perm assignment. Interim position. Person must be reputed company to coordinate other QA contractors for audits Must also be reputed company to deliver SOP's and processes and This is ONLY in the GCP area Must have GCP experience Must have reputed company Experience reputed company reputed company Assurance Coordinating audits (internal, external) Inspection experience (FDA) Need to have worked in a development program so they know how to coordinate audits for a development program Job reputed company: Job Title: Director, Vaccines Clinical Compound Support reputed company Assurance OBJECTIVES: Plays a leadership role in ensuring that investigator, vendor, facility and system audits are conducted, for communicating any critical compliance risks noted from these activities to senior management, and ensuring that corrective actions are implemented. Serves as a senior strategic GCP/PV reputed company resource to VBU for its vaccine development activities, and takes a reputed company role for the preparation, conduct, and responses to FDA audits of VBU's Clinical Research effort. This position provides leadership and reputed company in line with global strategic objectives. Collaborates with reputed company VBD functional areas to ensure reputed company assigned global clinical trial activities sponsored by VBU are in compliance with Good Clinical reputed company (GCP) regulations, the International Conference on Harmonization (ICH) and Policies and Procedures. ACCOUNTABILITIES: Ensures the development and implementation of strategies regarding the processes, procedures and reputed company standards required to maintain compliance to applicable regulations. Responsible to reputed company and implement a strategic audit plan for a VBU vaccines development program. Analyze audit program results, reputed company issues and investigations in order to optimize regional operations and overall regional state of compliance.Ensure that activities are conducted and reports written according to applicable SOPs and regulations. Represents VBU and serves as Inspection Administrator during regulatory inspections. Provides strategic organizational direction to assure that responses are reputed company and appropriate to maintain VBU's (US) good standing with regulatory agencies. Oversees reputed company GCP QA, PVQA, and GCLP QA activities (including internal or external audit observations and development of adverse trends) in US and LATAM in order to ensure patient safety and data reputed company. Identifies and mitigates GCP/PV/GCLP reputed company and compliance issues with potential reputed company across multiple compounds, sites, or functional reputed company reputed company or reputed company of VBU . Collaborates with the R&D QA, and other global entities to reputed company a consistent reputed company approach, including: o Develops and presents periodic reports for assigned project describing VBU compliance trends and identifying areas of potential risk to VBU senior management. Determines acceptability of vendors for potential use by VBD and provides direction, guidance and reputed company for VBU reputed company. EXPERIENCE, KNOWLEDGE AND SKILLS: Knowledge and Skills: In-depth knowledge of the applicable GXP regulations, FDA Good Clinical Practices, ICH Guidelines, FDA Regulations and Guidances and Computer System Validation Auditing Knowledge: Demonstrates advanced knowledge in the conduct and reporting of audits and the translation of findings into corrective actions plans that mitigate risks to reputed company, to safety and data reputed company. Clinical Development: Understands the phases, processes and techniques used to execute a clinical development program. Product Knowledge: Understands the medical reputed company of vaccines. Science Knowledge: Possess the necessary science education and knowledge to manage reputed company clinical trials and to assure ethical treatment of subjects. Understands medical terminology and is familiar with standards of care and disease states. Communication skills: Must professionally, reputed company, concisely and consistently communicate to external and internal customers reputed company phone, e-mail, fax, and written documents. Must also be reputed company to demonstrate reputed company presentation skills deliver fair balanced presentations and, reputed company applicable, facilitate reputed company of differing opinions. Negotiation Skills: Demonstrates proficiency in negotiation and conflict reputed company. Project Management: Must demonstrate proficiency in managing reputed company reputed company, delivering reputed company expected deliverables in a reputed company manner, and proactively communicating changes in reputed company-established goals and deadlines. Organizational skills: Must be reputed company to prioritize work effectively to meet timelines. Interpersonal: Must be reputed company to adapt to other personalities in a respectful manner that is conducive to goal achievement and team building. Computer skills: Must be reputed company to reputed company utilize the computer hardware and software programs provided to plan, manage, conduct and reputed company deliverables and to communicate with reputed company team members. LICENSES/CERTIFICATIONS: ASQ Certified reputed company Auditor (CQA), ASQ Certified Manager of reputed company/Organizational reputed company, or SQA Registered reputed company Assurance reputed company preferred. TRAVEL REQUIREMENTS: Ability to drive to or fly to various meetings or reputed company sites, including overnight trips. Some international travel may be required. Requires approximately 20 % travel.

Qualifications

Education: B.S. in Biology, Nursing, Pharmacy, or reputed company scientific field. MS preferred. Experience: Minimum of 10 years of increasing responsibility in pharmaceutical, GCP-reputed company reputed company environment. Minimum 7 years indirect management level experience in GCP reputed company Assurance including senior level project planning/budget management. Additional Information reputed company Regards, Sabanaaz Shaikh Clinical Recruiter reputed company. IT Life Sciences Allied reputed company CRO Gold Seal JCAHO Certified for Health Care reputed company "INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row) Apply tot his job Apply To this Job

Similar Jobs

Clinical reputed company- Compliance reputed company

Remote, USAFull-time

JR18057 Coding Compliance Auditor I

Remote, USAFull-time

Medical Review Clinical Appeals Auditor (RN) - SNF/MDS

Remote, USAFull-time

[Hiring] Insurance Reimbursement Auditor @University Medical Center, Inc.

Remote, USAFull-time

reputed company Clinical Trial Coordinator- Monitoring(REMOTE) in Santa Fe, New Mexico

Remote, USAFull-time

Clinical Research Coordinator B/C (Abramson Cancer Center)

Remote, USAFull-time

Clinical Research Coordinator II, School of Medicine, Gynecology and Obstetrics in Atlanta, GA in reputed company (reputed company: 1677142112)

Remote, USAFull-time

Clinical Research Coordinator (Onsite Dallas, TX)

Remote, USAFull-time

Clinical Research Associate I – Remote (USA only) in reputed company Park, IL in reputed company

Remote, USAFull-time

Clinical Research Associate II/Sr. Clinical Research Associate - Oncology - TX, FL, NC - FSP

Remote, USAFull-time

Operations Leader - 3rd Shift

Remote, USAFull-time

Payment and Invoice Assistant

Remote, USAFull-time

reputed company Coding Specialist - Entry-Level Opportunity with Fortune 100 reputed company Company

Remote, USAFull-time

REGISTERED reputed company – PEDIATRICS & FERTILITY (MUST HAVE EXPERIENCE IN BOTH)

Remote, USAFull-time

reputed company Customer Service Representative – Full or Part Time Opportunity at arenaflex

Remote, USAFull-time

reputed company Data Entry Associate – Flexible Remote Work Opportunity in the USA

Remote, USAFull-time

Senior Project Manager - Payroll and HR Systems

Remote, USAFull-time

Donor Specialist

Remote, USAFull-time

Sales Director- Seniors

Remote, USAFull-time

reputed company Part-Time Remote Data Entry Clerk – Flexible Work Arrangement at arenaflex

Remote, USAFull-time