Clinical Trial Manager 1 job vacancy in MCKESSON, (The Woodlands, TX 77380)

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We got a new job details in MCKESSON & they are Hiring Candidates for Clinical Trial Manager 1

Job Details
Company Name : MCKESSON
Company Location : The Woodlands, TX 77380
Job Position : Clinical Trial Manager 1
Job Category : Jobs in Texas

Job Description :
McKesson Corporation is a global leader in healthcare supply chain management solutions, retail pharmacy, community oncology and specialty care, and healthcare information solutions. McKesson partners with pharmaceutical manufacturers, providers, pharmacies, governments and other organizations in healthcare to help provide the right medicines, medical products and healthcare services to the right patients at the right time, safely and cost-effectively. United by our ICARE shared principles, our employees work every day to innovate and deliver opportunities that make our customers and partners more successful – all for the better health of patients. McKesson has been named a “Most Admired Company” in the healthcare wholesaler category by FORTUNE, a “Best Place to Work” by the Human Rights Campaign Foundation, and a top military-friendly company by Military Friendly. For more information, visit www.mckesson.com.

Serve as the clinical point person managing protocol execution.
Responsible for communication and escalation of study related issues as required.
Work cross-functionally to ensure clinical program timelines and goals are met.
Managing selective open to enrollment (registries, non-treatment, roll over, phase I-IV) and closed to enrollment studies.
Mentor Senior Clinical Trial Associate.
Exposure to study start up.
Ensure trial adherence to ICH/GCP/local regulations.
Review clinical trial budgets and Medicare coverage analysis (MCA) for alignment with protocol assessments and supporting protocol documents.
Communicate effectively with internal and external study personnel (investigative staff, vendors, etc.).

Facilitate sponsor and CRO associated vendors (e.g. IVRS, Reading Centers, etc.) to ensure appropriate site access and activation requirements are available.
Ensure availability of clinical/non-clinical supplies.

Ensure internal and external systems are updated in a timely manner (CTMS, clinicaltrials.gov).
Identify, address, and communicate quality and compliance concerns.

May participate in utilization and review of clinical systems (feasibility tools, new/enhanced CTMS models, data entry, etc.). Provide study-specific direction and mentoring to other staff as appropriate.

Other duties as requested

Minimum Job Qualifications (Knowledge, Skills, & Abilities):
Education/Training –

Bachelor’s degree in clinical or scientific discipline (or equivalent experience)
Required: Minimum of three years of clinical research experience
Preferred: Prior oncology research experience
Preferred: Study management/project management experience

Specialized Knowledge/Skills –

Attention to detail, solid execution, meeting aggressive timelines, strong interpersonal skills and team player.
Excellent verbal and written communication skills
Must be pro-active team player, flexible, and open to change.
Works in compliance with principles of Good Clinical Practice and applicable federal, state, and local regulations.
Preferred: Prior oncology research experience
Supports and adheres to the US Oncology Compliance Program, to include the Code of Ethics and

Business Standards.

Experience developing study plans and budgets including risk mitigation strategies
Experience in multiple phases of research preferred

Must be authorized to work in the US. Sponsorship is not available for this position.
We take pride in our culture of connection and believe in a workplace where everyone can be their full, authentic self. We welcome and encourage veterans, individuals with disabilities and others with diverse perspectives to join our growing team. Your unique perspective and experience are valuable assets that can translate into a rewarding career path with us. Apply to join our team and help shape the future of healthcare!

At McKesson, we care about the well-being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse employee population and ensure they are the healthiest versions of themselves. For more information regarding benefits at McKesson, please click here.

As part of Total Rewards, we are proud to offer a competitive compensation package at McKesson. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.

Our Base Pay Range for this position
$31.46 – $52.44

McKesson is an Equal Opportunity/Affirmative Action employer.

All qualified applicants will receive consideration for employment without regard to race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability, or protected Veteran status.Qualified applicants will not be disqualified from consideration for employment based upon criminal history.

McKesson is committed to being an Equal Employment Opportunity Employer and offers opportunities to all job seekers including job seekers with disabilities. If you need a reasonable accommodation to assist with your job search or application for employment, please contact us by sending an email to Disability_Accommodation@McKesson.com. Resumes or CVs submitted to this email box will not be accepted.

Current employees must apply through the internal career site.

Join us at McKesson!