Work with department leaders to ensure alignment among CAT operational and clinical services * Lead and/or contribute to departmental initiatives that aim to implement polices, methods, techniques to ...
Work with department leaders to ensure alignment among CAT operational and clinical services * Lead and/or contribute to departmental initiatives that aim to implement polices, methods, techniques to ...
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MannKind Corporation is currently seeking an experienced global trial lead, Clinical Operations to lead/support the design, planning, implementation and execution of clinical study protocols ...
Associate Director, Trial Lead Clinical Operations (Contract to Perm)
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... Health Clinical Engineering (THCE) program at Regional Health Ministry (RHM) Hospital and ... among associates across all functional areas. Provides consultative, operational, and technical ...
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... Health Clinical Engineering (THCE) program at Regional Health Ministry (RHM) Hospital and ... among associates across all functional areas. Provides consultative, operational, and technical ...
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MannKind Corporation is currently seeking an experienced global trial lead, Clinical Operations to lead/support the design, planning, implementation and execution of clinical study protocols ...
MannKind Corporation is currently seeking an experienced global trial lead, Clinical Operations to lead/support the design, planning, implementation and execution of clinical study protocols ...
The Associate Director, Clinical Services leads a team of Registered Professional Nurses and ... This position provides leadership, operational oversight, and relationship support for the clinical ...
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Clinical Executive Director
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$35.75 - $48.75/hr
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Quick apply
Associate Director, Clinical Development Trial Lead (CDTL)
Stamford, CT · On-site
$35.75 - $48.75/hr
Job Title: Associate Director, Clinical Development Trial Lead Location: Stamford, CT Type ... Drive regional clinical operational processes and methodologies used. Requirements * Bachelor ...
Associate Director, Clinical Development Trial Lead (CDTL)
Stamford, CT · On-site
$35.75 - $48.75/hr
Job Title: Associate Director, Clinical Development Trial Lead Location: Stamford, CT Type ... Drive regional clinical operational processes and methodologies used. Requirements * Bachelor ...
Quick apply
Associate Director, Clinical Development Trial Lead (CDTL)
Stamford, CT · On-site
$35.75 - $48.75/hr
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The Vice President, Associate General Counsel, Infectious Disease Franchise will be responsible for ... and Clinical Operations, Regulatory Affairs, Medical Affairs, Drug Safety, and Patient Advocacy ...
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Clinical Operations Associate information
See Connecticut salary details
$10.75 - $14.39
9% of jobs
$16.76 is the 25th percentile. Wages below this are outliers.
$14.39 - $18.02
24% of jobs
The median wage is $20.80 / hr.
$18.02 - $21.66
22% of jobs
$21.66 - $25.30
16% of jobs
$26.92 is the 75th percentile. Wages above this are outliers.
$25.30 - $28.94
9% of jobs
$28.94 - $32.58
7% of jobs
$32.58 - $36.21
4% of jobs
$36.21 - $39.85
4% of jobs
$39.85 - $43.49
3% of jobs
$43.49 - $47.13
1% of jobs
$47.13 - $50.77
0% of jobs
$10
$24
$50
How much do clinical operations associate jobs pay per hour?
What is a Clinical Operations Associate job?
A Clinical Operations Associate supports the planning, execution, and management of clinical trials to ensure compliance with regulatory guidelines and company protocols. They assist in coordinating trial logistics, managing documentation, and communicating with study sites and stakeholders. Their role helps ensure studies run efficiently, meet regulatory requirements, and generate reliable data for drug development and approvals.
What are the key skills and qualifications needed to thrive in the Clinical Operations Associate position, and why are they important?
To thrive as a Clinical Operations Associate, you need a solid background in clinical research processes, project management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is highly valued. Attention to detail, strong organizational skills, and effective communication are important soft skills that help manage complex studies and collaborate with cross-functional teams. These abilities are crucial for ensuring that clinical trials run smoothly, meet regulatory standards, and maintain participant safety.
What are the typical responsibilities and team dynamics for a Clinical Operations Associate?
As a Clinical Operations Associate, your typical responsibilities include coordinating study activities, maintaining trial documentation, supporting regulatory submissions, and ensuring adherence to protocols and timelines. You will often work as part of a multi-disciplinary team that includes clinical research coordinators, data managers, and study monitors, frequently communicating with internal and external stakeholders to keep the study on track. Collaboration and adaptability are key, as priorities can shift based on site needs or regulatory updates. This role offers valuable exposure to the operations side of clinical research and can serve as a springboard to more senior roles such as Clinical Project Manager or Clinical Research Associate.

Associate Director, Operations - Clinical Assessment Technologies (CAT) - US/Canada - Remote
Remote
Full-time
This job post has expired 1 day ago. Applications are no longer accepted.
Job description
Who we are
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
What the Business Development Operations Department does at WorldwideBusiness
Development Operations is a team of highly experienced Business Development professionals who drive significant bookings targets and support Worldwide’s strategic position in a competitive market through a culture of collaboration and innovation.
This tenured team supports a strong portfolio of existing business as well as being responsible for the continued significant growth of Worldwide’s future pipeline and sponsors. The team is accountable for overall sales performance, the profitable achievement of sales goals, and for aligning sales objectives with the Worldwide’s therapeutic and commercial strategies.
What you will do
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Identify operational needs for upcoming projects, track and review current assignments for CAT Operations staff
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Resource CAT study projects as Resource Manager
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Engage as Subject Matter Expert (SME) for CAT Operations activities
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Provide operational oversight for designated CAT study projects
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Engage in and coordinate resourcing activities for all CAT awarded projects
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Identify training and skills gaps among staff; coordinate and assist with learning opportunities to enhance operations staff knowledge and skills of industry related regulations, processes, materials, and guidelines
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Actively identify and engage in process improvement activities
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Participate in QMD reviews and new QMD development
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Author, collaborate, and review QMD documents and guidance documents
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Coordinate and manage CAT Operations team meetings
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Active engagement and oversight of study risk assessments, as they relate to operational activities
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Work with department leaders to ensure alignment among CAT operational and clinical services
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Lead and/or contribute to departmental initiatives that aim to implement polices, methods, techniques to contribute to existing service areas and department growth
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Accountable for oversight of CAT study deliverables from Launch process to study close out
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Assist and collaborate with Operations staff, Project Management, Contracts on vendor and study budget development, scope of work revisions, tracking and compliance
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Assist in vendor management related concerns, including involvement with escalations, Vendor Management and Quality Assurance meetings
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Review and assess ongoing budget utilization and revenue recognition with Operations Managers to ensure projects are meeting financial targets
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Manage internal CAT operations meetings and other trial-specific meetings, as appropriate
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Significant contributor to multiple strategic departmental, sponsor-related and cross-functional initiatives
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Participate in business development activities including; but not limited to proposals input, capabilities, and bid defense meetings
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Apply thorough knowledge of industry regulations and guidelines to ensure operational compliance during clinical trial conduct
What you will bring to the role
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Exceptional organizational skills, detail- and service-oriented, with excellent management / supervision skills
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Excellent understanding of best business practices with respect to clinical trial operations and rater reliability processes
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Knowledge and capabilities of our technology vendors and their abilities (skill)Excels in planning, managing, monitoring, and critiquing skills
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Excellent at meeting timelines consistently and being able to effectively work under pressure
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Continuously open to constructive, developmental feedback
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Exceptional interpersonal skills in a fast-paced, deadline oriented, and changing environment
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Excellent ability to proactively identify and escalate potential project issues to appropriate CAT and WCT staff
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Basic knowledge of statistics and finance practices
Your experience
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Must have a minimum of a bachelor’s degree, preferably with an Master’s degree (life sciences, MBA and/or PMP certification).
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Strong leadership, management and interpersonal skills
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Strong planning and organizational skills
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At least 7+ years clinical trial experience with at least 4 years’ experience in global clinical trials
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Preferred at least 5+ years of experience managing team members or project management experience
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Hands on experience in day-to-day management of all aspects of global clinical trials required
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Prior experience in psychiatry / CNS therapeutic areas is a plus
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The ideal candidate possesses knowledge and appreciation of all stages of clinical drug development. Effective leadership skills and a proven ability to build and foster high performance team productivity and cohesiveness is required. This position requires strong knowledge of monitoring practices, demonstrated knowledge / competence in the application of CFRs, GCPs and ICH guidelines
At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):
United States of America - $112,000.00 - $223,000.00
The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
About Worldwide Clinical Trials
Sourced by ZipRecruiter
Industry
Scientific research and development services
Company size
10,000+ Employees
Headquarters location
Durham, NC, US
Year founded
1986