Clinical Trial Manager

Description

The Clinical Trial Manager (CTM) will support successful and timely start-up and completion of clinical trials and be a key member of the Organization of Chief Medical Officer (OCMO) Global Clinical Affairs team This includes managing the day-to-day execution of clinical studies for in vitro diagnostics (IVDs) and medical devices (MDs) ensuring Good Clinical Practice (GCP), and adherence to Agilent procedures, and all applicable regulations.

The CTM will build strong internal and external relationships, including with clinical sites, and collaborate with cross functional team members.

The CTM will report to a Clinical Operations Manager, Senior Manager, or Director, depending on level and needs of the business.

Primary Responsibilities (all levels) :

Manage design and implement all clinical operational aspects of IVD clinical trials from inception through close-out

Serve as main point of contact for internal and external study stakeholders; effectively communicating, collaborating, managing escalation of issues, where necessary, as well as participating and leading internal and external study meetings

Identify, evaluate, and oversee qualification and contracting for study investigators, study sites, CRO and / or vendor management for the study

Develop or assist in the development of study-related plans and documents including protocols, informed consent forms, monitoring plans, case report forms, training plans and engagement materials

Ensure trial master file (TMF / eTMF) is established, current, and maintained per ICH E6(R2). May coordinate study IRB / EC approvals

Support Clinical Research Associates (CRAs) to ensure proper site training and management, provide ongoing oversight of clinical site compliance with study plans, study protocol, internal SOPs, FDA CFR, ICH / GCP guidelines, and in compliance with all applicable regulations.

Demonstrate compliance with and enforcement of these regulations and requirements

Manage study deliverables and track study metrics including identifying potential risks to study timelines and / or conduct

Participate in data management activities, such as CRF development, training, and facilitating query resolution

Lead or contribute to organizational and departmental process development, improvement, and implementation

Provide guidance and mentorship to junior team members

Qualifications

Bachelor's degree or higher, or equivalent credentials

Knowledge of GCP, ICH guidelines, and other clinical regulatory requirements

Strong interpersonal skills (verbal and written), organizational, and prioritization skills, able to communicate at multiple levels of an organization and with sponsors / clients.

Ability to work independently and effectively in a fast-paced environment

Strong work ethic and ability to deliver tasks on time

Proficient with office automation tools, especially Microsoft PowerPoint, Excel and Word.

People management skills

For CTM : 1+ year of direct clinical study management experience or 4+ years of direct clinical operations experience with sponsor, CRO and / or companion diagnostics, device manufacturer, IVD, or similar industry(ies) demonstrating management or study lead experience with a track record of successful trial initiation and execution, or equivalent experience.

LI-PK1

Additional Details

This job has a full time weekly schedule. It includes the option to work remotely. Applications for this job will be accepted until at least October 17, 2024 or until the job is no longer posted.

The full-time equivalent pay range for this position is $97, - $180, plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location.

Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training.

During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at : Agilent Technologies, Inc.

is an Equal Employment Opportunity and Affirmative Action employer. We value diversity at all levels. All individuals, regardless of personal characteristics, are encouraged to apply.

All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases.

Agilent Technologies, Inc., is committed to diversity in the workplace and strives to support candidates with disabilities.

If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email or contact +1-262-754-5030.

For more information about equal employment opportunity protections, please visit

Travel Required

25% of the Time

Shift

Duration

No End Date

Job Function

Medical / Clinical