Match score not available

Clinical Trial Manager II-Biotech-United States, Remote

EXTRA HOLIDAYS - EXTRA PARENTAL LEAVE

Remote:

Full Remote

Contract:

Full time

Experience:

Senior (5-10 years)

Work from:

Greece, United States

Offer summary

Qualifications:

2+ years in Clinical Trial Management role at a CRO, Bachelor's Degree in health or life sciences, 8+ years relevant experience required, 2+ years of monitoring experience preferred, Experience managing complex or global trials preferred.

Key responsabilities:

Oversee clinical budget for resource allocation
Develop monitoring plans for effective oversight
Train and mentor CRAs to optimize performance
Drive enrollment and manage study start-up activities
Foster relationships with Sponsors and cross-functional teams

ICON plc Pharmaceuticals XLarge https://www.iconplc.com/

10001 Employees

HQ: Dublin

See more ICON plc offers

Job description

Your missions

Clinical Trial Manager II Biotech- United States-Remote

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

We are currently seeking a CTM II to join our diverse and dynamic Biotech team with a therapeutic alignment of Gen Med. As the CTM II, you will hold a crucial role in ensuring the successful delivery of all clinical aspects of the studies.

What You Will Be Doing:

Budget Oversight Oversee the clinical portion of the budget to ensure efficient resource allocation.
Ensuring Effective Study Oversight: Develop monitoring plans and tools, ensuring effective study oversight.
Optimizing Performance: Train and mentor Clinical Research Associates (CRAs) to optimize their performance.
Timely Study Start-Up & Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines.
Improving Study Integrity Review trip reports and implement corrective and preventative action plans when necessary.
Building Productive Relationships: Foster productive relationships with Sponsors, vendors, and cross-functional teams.

Your Profile:

Level 2:

2+ years in a Clinical Trial Management position at a CRO, Required
Bachelor’s Degree in a health, life sciences or other relevant field of study, required
8+ years of relevant experience, required
2+ years of monitoring experience, strongly preferred
Experience in managing complex or global trials, preferred
Current/Prior Various Gen Med experience
Experience in managing all trial components (start-up to database lock), preferred
Experience in coaching/mentoring other CTMs, leading a team of CTMs, participating in departmental initiatives, preferred
English fluency (ability to read, write, speak), required
Travel of up to a maximum of 10%, required

#LI-TG2

#LI-REMOTE

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply