Job Description

PLEASE NOTE: Must be authorized to work lawfully in the United States for any employer without sponsorship. For immediate consideration, please apply.

Kelly® Science & Clinical is seeking a Clinical Research Project Manager – Diagnostic for a direct hire position at a leading client in Van Nuys, CA. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.

Pay Rate:

$90-130,000/Year (commensurate with experience)

Overview:

Our client, who is a biobank and laboratory CRO, supports the largest In Vitro Diagnostic companies in the industry. They are hiring a permanent Project Manager to work onsite in Los Angeles, California. In this role, you will design and execute IVD sample collection trials to ensure that agreed upon services are delivered on time and on budget using a network of physicians and labs to achieve client satisfaction. The Project Manager will perform all job functions in accordance with the CRO standard operating procedures and policies, Good Clinical Practice guidelines, and all applicable regulatory requirements.

• Clinical Trials Division

• Reports to: SVP of Operations

Schedule:

Friday – Monday, 1 st /Day: Standard Hours

Responsibilities:

• Design and document a project plan with details for each site and any labs including details for (sites selected, # kits per site, detailed CTMS setup in Salesforce, lab coordination, shipping, etc.).

• Responsible for evaluating and communicating the impact of any risks and developing plans to mitigate these risks.

• Manage Clinical studies as Project Owner for all assigned studies, as outlined in the Clinical Studies process, with accountabilities/authorities specified in the process map including ensuring protocol and study design are feasible, develop and train team on the project plan, risk mitigation plans, CRF development, kit design with service getting from kit making team, support budget/contract negotiation with sites and service from Site Network Manager, regulatory document management, and maintaining and suggesting improvements to Clinical studies process documentation.

• Design protocols to be approved by the IRB quickly that meet client requirements, prevent unnecessary deviations, and allow for internal and client flexibility.

• Define and recommend top priorities for all projects on a rolling weekly basis.

• Ensure team members supporting study activities are working on these priorities, escalating any issues or prioritization question with service providers to manager.

• Design and ensure case report forms can capture client requested data, allow them to audit, and are clear for doctors to avoid doctor errors and minimize the number of queries.

• Provide options to clients for kit materials and design.

• Develop SIV training materials to clearly define the steps of the study and how it is conducted.

• Conduct or ensure training for all relevant site staff.

• Conduct and/or ensure clinical "visits" including site qualification, clinical training/SIV, and site close outs.

• Ensure all clinical studies and sites receive IRB approval within two weeks for new submissions.

• Proactively monitor project status and address issues, potential risks, and client inquiries/requests in a timely manner, which may occasionally require a flexible work schedule/working outside of normal business hours.

• Keep track and resolve client requests as study progresses.

• Host/attend client calls on time/early especially when hosting.

• Host/support client visits and audits/inspections.

• Review each project, balancing requirements with current workload, and recommending additional resources including time or reprioritization that will help enable new studies.

• Ensure CRA are generating site payments and client invoices monthly.

• Review/approve site payments prior to submission to doctors.

• Ensure successful execution of data management activities (eCRF, manifest, test file).

• Review shipping manifests and contents of shipping containers

Qualifications:

• A minimum of 5 years of industry experience and a minimum of 2 years clinical study management.

• Knowledge of accepted good clinical research practice (GCP) and procedures.

• Experience with in vitro diagnostics and/or medical device industry for diagnostic devices.

• Excellent organizational, time management, budget management, and problem-solving skills.

• Hustle: Comfortable in a fast-paced small company environment and able to adjust workload based upon changing priorities.

• This is an onsite position with little to no travel.

What Happens Next:

Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry – even if this position doesn’t work out, you’re still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.

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As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

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