Associate Clinical Project Manager, Sponsor Dedicated at IQVIA

Parsippany, New Jersey, United States

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceutical, Clinical ResearchIndustries

Requirements

Bachelor's Degree in life sciences or related field
2 years of clinical trial management experience in a role accountable for driving and owning local trial activities at the regional level
Expertise in drafting and managing informed consent process
Expertise in managing site selection
Expertise in patient recruitment strategies
Expertise in monitoring visit reports
Expertise in driving risk-based mitigation plans
Reside in the same country where the job is located (home-based position)

Responsibilities

Provide input into 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, ensuring consistent use of study tools, 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
Collaborate with other functional groups within the company to support milestone achievement and 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 to external stakeholders
Identify risks (positive and negative) and contingencies; 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 partnering with project leader to plan/implement corrective and preventative action plans
Serve as primary (for small projects) or back-up project contact with customer
Lead the efforts of a project sub-team, managing cross-collaboration to support milestone achievement and 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
Identify lessons learned and implement best practices
May be assigned as the primary contact for vendors, leading project vendor management and related activities as per project requirements
Provide country-level oversight of clinical trials from study start-up through database lock and closeout
Ensure high-quality data delivery and regulatory compliance across all phases of the trial
Maintain inspection readiness and uphold GCP, SOP, and local regulatory standards

Skills

Key technologies and capabilities for this role

Clinical Trial ManagementInformed ConsentSite SelectionPatient RecruitmentMonitoring Visit ReportsRisk-Based MitigationGCPSOPRegulatory ComplianceStudy Management Plans

Questions & Answers

Common questions about this position

Is this a remote position?

Yes, this is a home-based position, but you must reside in the same country where the job is located to be eligible.

What experience is required for this role?

Two years of clinical trial management experience is required in a role accountable for driving and owning local trial activities at the regional level.

What key skills are needed to thrive in this position?

Candidates need expertise in drafting and managing informed consent processes, managing site selection, patient recruitment strategies, monitoring visit reports, and driving risk-based mitigation plans.

What is the salary or compensation for this role?

This information is not specified in the job description.

What does the company culture or team environment look like?

The role operates in a fast-paced environment with evolving priorities, as part of a core project team collaborating closely with cross-functional teams to deliver clinical trials, ensure quality, and achieve operational excellence.

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters

1998Year Founded

$3,526MTotal Funding

POST_IPO_EQUITYCompany Stage

Cybersecurity, Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.

Proliferation of disparate technological solutions causes technology overload in clinical trials.

Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.

The company offers privacy-enhancing technologies to protect individual patient data.

IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.

AI-driven drug discovery accelerates identification of potential drug candidates.

Expansion of telemedicine facilitates remote patient monitoring and data collection.

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