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10 days old

Clinical Project Manager (Sr. Manager, Clinical Operations)

Kelly Services
Deerfield, IL 60015
Kelly Services is currently seeking a Clinical Project Manager (Sr. Manager, Clinical Operations) in Deerfield, IL to work a contract assignment of 12 months for one of our top clients. Kelly is a full service workforce solutions provider to 98% of the Fortune 100 companies. We provide employment to more than 700,000 people annually and we deal with some of the largest and best companies both nationally and locally.



**Primary Responsibilities of the** Clinical Project Manager (Sr. Manager, Clinical Operations) **includes:**




+ The primary responsibility is to manage both national and global clinical trials and their associated clinical teams including timelines and budget for clinical trial execution and ensuring clinical trials are conducted in accordance with the company's Global Clinical Development procedures, ICH GCP Guidelines, the Declaration of Helsinki and national regulations.

+ May represent Global Clinical Development on Project Development Core Teams for drug and device programs, supporting studies through for regulatory approval. Reports directly to the Director of Global Clinical Operations.

+ Able to work independently to manage all aspects of a clinical trial from site selection/vendor selection process to database lock and review of the final clinical study report. Activities including management of product inventory, forms development, enrollment, budget, and timeline projections.

+ Manage the interfaces with Legal, Global Project Management, Data Management, Medical Writing, Clinical Supply, Clinical Compliance and Training, Pharmacovigilance, and Biostatistics.

+ Effectively manage external team/vendors activities including CRO, central lab, IRB and other external contractors.

+ Interact effectively with Sr. Management to provide updates and communicate issues.

+ Review other study documents such as protocols, Investigators brochures, DMPs, CRFs, SAPs, and CSR.

+ Clinical Plan - Partner with the Medical Monitor and Regulatory Affairs to prepare a clinical plan for each project. This includes preparing timelines and budgets for the clinical program.

+ Clinical Trial Protocols - Prepare directly or facilitate preparation of protocols including study design, case report forms, study procedures. Develop and complete enrollment feasibility evaluations based on protocol synopsis. Draft informed consents based on study and regulatory requirements.

+ Research Agreements and Study Budgets - negotiate study budgets with sites.

+ Identify clinical investigators and assess suitability of study sites. Recognize and maintain strong business relationships with key opinion leaders.

+ Plan and conduct investigators meetings.

+ Order clinical supplies and ensure logistics plans are in place prior to study start.

+ Train study staff on product usage, data collection and specific procedures.

+ Comprehensive knowledge and understanding of European/FDA regulations and ICH Guidelines for Good Clinical Practices required.

+ Ability to maintain effectiveness under changing circumstances and priorities. Tact and diplomacy is a strength.

+ Excellent verbal and written communication and organizational skills required.

+ Knowledge of computer software and meticulous attention to detail expected for this position.

+ Confident decision-making and ability to work effectively as a team leader, team member, or individually.

+ Proficiency in data collection design, scientific evaluation and clinical planning.

+ Demonstrated ability to represent Clinical Operations in global project teams, execute clinical strategies and manage complex programs in a fast paced milestone focused environment.

+ Has a track record of delivering on commitments. Capable of handling (assimilating) in-depth technical information from a variety of disciplines in order to be scientifically credible within the global team.

+ Has working knowledge and familiarity with US Federal Food and Drug Administration, ICH/GCP, and European Regulatory Authority requirements as applicable to a study.

+ Excellent verbal and written communication skills required. Interpersonal and organizational skills a must.

+ Ability to multitask with a strong attention to detail.

+ Possess working knowledge of research objectives, protocol design and data collection standards.

+ Must demonstrate leadership skills in order to direct clinical team in study preparation and execution.

+ Comprehensive understanding of the drug/device development process.

+ Solid technical basis in pharmaceutical development and delivery systems technologies.

+ Proven ability in planning and conducting clinical trials.

+ Software: MS Word, Excel (pivot tables, v-lookups), Outlook, PowerPoint, SharePoint, MS Project

+ Position allows for flexibility in work week with ability to work from home up to 2 days/week at supervisors discretion.

+ Consultant must successfully meet criteria required for Clinical Project Manager job positions.

+ This consultant will often be utilized for moderate to large (sometimes global) projects where project delays and/or efficiencies bring risk financially and/or to client reputation.



Looking for:

1. Pharma/med device PM experience

2. Project management experience 3 years plus

3. CRO over-site

4. Software skills

5. Experience with successfully driving results

6. Local candidates, strongly preferred.



**Education and Experience Requirement of the** Clinical Project Manager (Sr. Manager, Clinical Operations) **includes** :




+ BS in scientific discipline + 5 years pharmaceutical and/or device clinical development experience with 3+ years project management experience.



**Additional Information:**




+ Contract assignment, duration 12 months.

+ Work schedule: full-time, first shift.



**Kelly Temporary Employee Perks:**




+ Group medical, prescription, vision, dental, life, and short-term disability insurance options that are available for purchaseand the coverage is portable*

+ Service bonus plan and Holiday pay plan, if qualified

+ Weekly electronic pay options

+ Free online training campus available

+ Exclusive online employee community

+ Corporate discounts



**Apply Now!**



This position is recruited for by a remote Kelly office, not your local Kelly branch. To be considered for this position you must submit your resume to the Scientific Recruiter listed below:



**Please email your resume directly** to Sandy at: Sanm174@KellyServices.com [reference BH Job #1734527]



Thank you for your interest in the assignment.






**Why Kelly** **** **?**



Kelly Science is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interestsits the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.


**About Kelly** ****



At Kelly, were always thinking about whats next and advising job seekers on new ways of working to reach their full potential. In fact, were a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live. Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.


Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity. Equal Employment Opportunity is The Law. at https://www.dol.gov/ofccp/regs/compliance/posters/ofccpost.htm

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Posted: 2020-05-22 Expires: 2020-06-22

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Clinical Project Manager (Sr. Manager, Clinical Operations)

Kelly Services
Deerfield, IL 60015

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