Parsippany, New Jersey, United States · Remote OK
$93k–$233k/yr
*Home-based position - To be eligible for this position, you must reside in the same country where the job is located. Position Specifics This sponsor-dedicated role provides country-level oversight of clinical trials fr…
Skills: Clinical Trial Management, GCP, SOP, Risk-Based Mitigation, Site Selection
Parsippany, New Jersey, United States · Remote Solely
$68k–$233k/yr
*Home-based position - To be eligible for this position, you must reside in the same country where the job is located. Position Specifics This sponsor-dedicated role provides country-level oversight of clinical trials fr…
Skills: Clinical Trial Management, GCP, SOP Compliance, Risk Mitigation, Site Selection
Parsippany, New Jersey, United States · On-site
Position Title: Mobile Medical Assistant / Phlebotomist – Per Diem, In-Home Services Location: Various U.S. locations (local travel within designated geographic area) About the Role: IQVIA’s In-Home Clinical Solutions te…
Skills: Phlebotomy, EKG, Macular Edema Screening, Specimen Collection, Patient Care
Phoenix, Arizona, United States · On-site
Position Title: Mobile Medical Assistant / Phlebotomist – Per Diem, In-Home Services Location: Various U.S. locations (local travel within designated geographic area) About the Role: IQVIA’s In-Home Clinical Solutions te…
Skills: Phlebotomy, EKG, Macular Edema Screening, Specimen Collection, Patient Care
Boston, Massachusetts, United States · On-site
Job Overview Includes providing education to health care prescribers and their staff on the proper use of designated treatments for assigned disease area or reinforcement of study protocols as related to a clinical trial…
Skills: Phlebotomy, Clinical Trial Protocol, Customer Relationship Management, MS Office, Public Speaking
Parsippany, New Jersey, United States · Hybrid
$132k–$165k/yr
Acute Care Technology At ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, softwa…
Skills: System Architecture, Medical Device Design, Embedded Software, Electrical Engineering, Mechanical Engineering
Parsippany, New Jersey, United States · On-site
Position Title: Mobile Medical Assistant / Phlebotomist – Per Diem, In-Home Services Location: Various U.S. locations (local travel within designated geographic area) About the Role: IQVIA’s In-Home Clinical Solutions te…
Skills: Phlebotomy, EKG, Macular Edema Screening, Specimen Collection, Patient Care
Parsippany, New Jersey, United States · On-site
Position Title: Mobile Nurse (LPN/LVN) – Per Diem, In-Home Services Location: Various U.S. locations (local travel within designated geographic area) About the Role: IQVIA’s In-Home Clinical Solutions team seeks a qualif…
Skills: Phlebotomy, Electrocardiograms (EKG), Macular Edema Screening, Patient Care, Clinical Documentation
Cherry Hill, New Jersey, United States · On-site
$120k–$210k/yr
Are you a visionary scientific strategist capable of turning complex clinical data into impactful Medical Affairs communication plans? We are seeking a Strategic Director, Medical and Scientific Affairs to serve as a sen…
Skills: Medical Affairs Strategy, Client Leadership, Omnichannel Engagement, Insight Synthesis, Scientific Storytelling
Parsippany, New Jersey, United States · On-site
$23/hr–$42/hr
You’ve invested a lot of time and energy in your education. Now you want the chance to make your mark. We offer challenging opportunities for you to learn and grow professionally. In our programs, you’ll be immersed in a…
Skills: Prescription Fulfillment, Patient Counseling, Immunization Administration, Drug Utilization Review, Patient Safety
Tallahassee, Florida, United States · Hybrid
$75k–$166k/yr
We’re building a world of health around every individual — shaping a more connected, convenient and compassionate health experience. At CVS Health®, you’ll be surrounded by passionate colleagues who care deeply, innovate…
Skills: Medicare Compliance, Medicaid Compliance, Project Management, Regulatory Analysis, Auditing
Foster City, California, United States · Hybrid
$255k–$364k/yr
We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and…
Skills: Clinical Development Strategy, Medical Monitoring, Oncology Drug Development, Regulatory Submissions, Cross-functional Leadership
Foster City, California, United States · Hybrid
$206k–$293k/yr
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve l…
Skills: Biostatistics, Clinical Trial Design, SAS, R, Drug Development
Parsippany, New Jersey, United States · On-site
CHHA Case in Newton!!!! are you a compassionate Home Health Aide looking for a rewarding, good case, good hours close to home? Bayada Home Health Care is looking for a dedicated Certified Home Health Aide (CHHA) to join …
Skills: Activities Of Daily Living, Light Housekeeping, Range Of Motion Exercises, Bathing, Grooming
Chicago, Illinois, United States · On-site
$135k–$145k/yr
Health Information Technology Specialist Player Coach Do you have a passion for harnessing technology to make a positive impact on patients’ lives? Do you have Electronic Healthcare Record (EHR) as well as coaching, ment…
Skills: EHR Software, Team Leadership, Coaching, Mentoring, Workflow Assessment
Phoenix, Arizona, United States · On-site
$125k–$135k/yr
Health Information Technology Specialist Do you have a passion for harnessing technology to make a positive impact on patients’ lives? Do you have Electronic Healthcare Record (EHR) experience and are looking for a rewar…
Skills: EHR Software, Workflow Assessment, Problem Solving, Presentation Skills, Oral Communication
Parsippany, New Jersey, United States · Hybrid
$237k–$340k/yr
Job Description: As a privately-owned, biopharmaceutical company, Ferring pioneers and delivers life-changing therapies that help people build families and live better lives. Our independence helps us cultivate an entrep…
Skills: Global Medical Strategy, Reproductive Medicine, Clinical Trial Oversight, Life Cycle Management, Evidence Generation
Chicago, Illinois, United States · On-site
$125k–$135k/yr
Health Information Technology Specialist Do you have a passion for harnessing technology to make a positive impact on patients’ lives? Do you have Electronic Healthcare Record (EHR) experience and are looking for a rewar…
Skills: EHR Software, Epic, Cerner, Meditech, McKesson
Parsippany, New Jersey, United States · On-site
$85k–$115k/yr
We are seeking a motivated and results-driven Pharmaceutical Sales Representative to join our team. In this role, you will be responsible for driving volume and market share growth for assigned pharmaceutical products wi…
Skills: Pharmaceutical Sales, B2B Sales, Relationship Building, Sales Presentations, Account Planning
Parsippany, New Jersey, United States · On-site
$20/hr–$30/hr
Pay: $20–$30 per hour Schedule: Flexible schedule / After‑school hours Setting: Home‑based cases / Clinic cases About Circle Care Services Circle Care Services provides compassionate ABA therapy for children on the autis…
Skills: ABA Therapy, Behavior Intervention, Data Collection, Child Development, Patient Care
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Provide country-level oversight of clinical trials from start-up through closeout, ensuring high-quality data delivery and regulatory compliance. Collaborate with cross-functional teams to manage study milestones, mitigate risks, and maintain inspection readiness.
Requires a Bachelor's degree in life sciences and at least three years of clinical trial management experience. Must possess strong knowledge of ICH GCP, local regulatory laws, and effective communication skills.
*Home-based position - To be eligible for this position, you must reside in the same country where the job is located.
This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up through database lock and closeout. Operating in a fast-paced environment with evolving priorities, the role ensures high-quality data delivery and regulatory compliance across all phases of the trial.
Candidates who will thrive in this role have expertise in drafting and managing informed consent process, managing site selection, patient recruitment strategies, and monitoring visit reports, while driving risk-based mitigation plans to proactively address study challenges. The position collaborates closely with cross-functional teams to support trial execution, maintain inspection readiness, and uphold GCP, SOP, and local regulatory standards.
Three years of clinical trial management experience is required within a role that is accountable for driving and owning local trial activities at the regional level.
Additional Information
Associate Clinical Project Managers (aCPM)/Local Trial Managers are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The aCPM is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. The aCPM supports the efforts of CPM to drive operational excellence and strategic leadership with our customers.
Provide input in to the development of integrated study management plans with the core project team and/or sub-team.
Accountable for assigned portion of clinical studies as per the contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
Set objectives of project sub-team(s), according to agreed upon contract, strategy and approach, effectively communicate and assess performance.
Strong site engagement qualifications – able to interact with and drive change to address out of compliance sites.
Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
Monitor progress against contract and prepare/present project and/or sub-team information proactively to internal stakeholders. Support the project leader to prepare/present project and/or sub-team information proactively to external stakeholders.
Work with monitors to address systemic site issues.
Identify risk (positive and negative) and contingencies and partner with project leader in problem solving and resolution efforts.
Achieve project quality by identifying quality risks and issues, responding to issues raised by project sub-team members and partner with project leader planning/implementing appropriate corrective and preventative action plans.
May serve as primary (for small projects) or back-up project contact with customer.
Lead the efforts of a project sub-team, responsible for managing cross-collaboration of the sub-team to support milestone achievement and to manage issues and obstacles.
Support the project leader in ensuring the financial success of the project.
Forecast and identify opportunities to accelerate activities to bring revenue forward in partnership with the senior project leader.
Identify changes in scope and partner with project leader to manage change control process as necessary.
Identify lessons learned and implement best practices.
May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.
Bachelor's Degree In life sciences or related field required
3 years clinical trial management experience
Requires intermediate level knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education combined with experience
Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge, therapeutic knowledge desired.;
Communication - Strong written and verbal communication and ability to facilitate information sharing amongst stakeholders. Strong presentation skills.
Problem solving - Strong problem solving skills.
Proven ability to drive change management and follow through on changes to resolution
Organization - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.
Prioritization - Ability to handle conflicting priorities.
Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output.
IT Skills - Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint.
Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients. Strong customer service skills.
Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences.
Finances - Good understanding of project financials.
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 https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Offices: 2400 Ellis Rd, Durham, North Carolina 27703, US
Based on 121 listings with disclosed salaries, most healthcare jobs in Parsippany, NJ pay between $70k–$239k per year. Individual offers vary with seniority, company size, and specialization.
There are currently 173 open healthcare positions in Parsippany, NJ listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include IQVIA, Ferring Pharmaceuticals, Gilead Sciences, CVS Health, Kite Pharma, among others. Browse the listings above to see every active employer.
Yes — 53 of the 173 open healthcare positions offer remote or hybrid work (11 remote, 42 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
