Covers a wide range of medical, dental, and vision expenses to keep you and your family healthy.

Comprehensive Health Insurance 

Enjoy vacation days, personal leave, and holidays to relax and recharge without losing income.

Paid Time Off

Helps you save for the future with employer contributions and tax advantages.

Retirement Savings Plan

Access to training programs, workshops, and courses to enhance your skills and career growth.

Professional Development Opportunities

Options for remote work, flexible hours, or compressed workweeks to support work-life balance.

Flexible Work Arrangements

Provides confidential counseling and support services for personal and professional challenges.

Employee Assistance Program

IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and contract research services for the life sciences industry. By partnering with pharmaceutical, biotechnology, and medical device companies, IQVIA integrates vast data sets and extensive expertise to enhance research and development, commercial strategies, and patient engagement. With a presence in over 100 countries, IQVIA is committed to leveraging innovation and analytics to drive excellence in healthcare.

Source: <a href="https://www.iqvia.com/" target="_self">https://www.iqvia.com/</a>

About Us

At IQVIA, we believe meaningful progress starts with people—innovators, problem-solvers and collaborators who bring their unique perspectives to tackle the biggest challenges faced by the life sciences and healthcare. Together, we’re shaping a smarter, more connected ecosystem of talented people that positively impact patients everywhere, every day.

Source: <a href="https://www.iqvia.com/" target="_self">https://www.iqvia.com/</a>

Our Culture

Job Responsibilities: <ul><li>Serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, RSU Team Lead, Clinical Operations, Feasibility, Site Identification, Project Leadership and GICS. Ensure adherence to standard operating procedures (SOPs), work instructions (WIs), quality of designated deliverables and to project timelines. Where applicable, act as a Country Lead for projects with no regional Lead assigned.</li><li>Perform Regulatory, Start-up and Maintenance activities according to applicable regulations, SOPs and work instructions.</li><li>Prepare site regulatory documents, reviewing for completeness and accuracy.</li><li>Review, prepare and negotiate site contracts and budgets with sites, if applicable.</li><li>Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.</li><li>Ensure contracts are fully executed, regulatory documents and approvals are granted, IP Release authorized and specific project deliverables are completed.</li><li>Review and provide feedback to management on site performance metrics.</li><li>Review, establish and agree on project planning and project timelines. Ensure overall project efficiency and adherence to project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.</li><li>May contribute to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required.</li><li>May assist in pre-award activities including bid defenses, proposals and oversights of the scope of work at country level.</li><li>May provide input into contract and budget template development.</li><li>May support importation activities.</li><li>May have direct contact with sponsors on specific initiatives.</li><li>May act as Local Regulatory, Ethics and Contract Expert and reviewer of ICF.</li><li>May act as mentor, and prepare and deliver country-specific training, for less experienced staff.</li><li>May participate in feasibility and/or site identification activities.</li><li>May perform Site Selection Visits if a trained monitor.</li></ul>Job Requirements:<ul><li>Bachelor’s Degree in life sciences or a related field and 3 years’ clinical research or other relevant experience; or equivalent combination of education, training and experience.</li><li>In-depth knowledge of clinical systems, procedures, and corporate standards.</li><li>Good negotiating and communication skills with ability to challenge, if applicable.</li><li>Effective communication, organizational, and interpersonal skills.</li><li>Ability to work independently and to effectively prioritize tasks.</li><li>Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.</li><li>Knowledge of applicable regulatory requirements, including local regulations, , SOPs and company’s Corporate Standards.</li><li>Understanding of regulated clinical trial environment and knowledge of drug development process.</li><li>Ability to establish and maintain effective working relationships with coworkers, managers and clients</li></ul>IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at <a href="https://jobs.iqvia.com/" target="_blank">https://jobs.iqvia.com</a>

This job is a Site Activation Specialist, where you&#x27;ll be the go-to person for clinical studies. You might like this job because you’ll work with diverse teams, manage contracts, and ensure projects run smoothly while making a difference in healthcare!

Job Responsibilities: 

-Serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, RSU Team Lead, Clinical Operations, Feasibility, Site Identification, Project Leadership and GICS. Ensure adherence to standard operating procedures (SOPs), work instructions (WIs), quality of designated deliverables and to project timelines. Where applicable, act as a Country Lead for projects with no regional Lead assigned.

-Perform Regulatory, Start-up and Maintenance activiti...

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