Top 294 Clinical trial manager Jobs in Us & Remote

Clinical Trial Manager
Medilink Therapeutics —Remote
- $120,000 - $200,000 a year
- Full-time
- Nursing
- Microsoft Excel
- Bachelor's degree
- Health savings account
- Health insurance
Quick Apply
10d
Clinical Trial Manager, Clinical Operations
Bristol-Myers Squibb —Remote
- $134,505 - $162,988 a year
- Email
- Remote
- 5 years
- Bachelor of Science
- Bachelor's degree
- Paid holidays
- Disability insurance
Senior Clinical Trial Manager
Aveera Medical —Remote
- $125,000 - $175,000 a year
- Full-time
- Remote
- 7 years
- Organizational skills
- Senior level
- Health insurance
- Dental insurance
Quick Apply
Clinical Trial Manager, Immunology
Syncromune —Remote
- $145,000 - $165,000 a year
- Full-time
- Background check
- Nursing
- 5 years
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3d
Clinical Trial Manager, Immunology
SAB —Remote
- $150,000 - $165,000 a year
- Full-time
- Remote
- 6 years
- Bachelor of Science
- Bachelor's degree
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8d
Clinical Trial Manager
Oura —Remote
- $79,900 - $110,000 a year
- Remote
- 3 years
- Travel
- Contracts
- Paid holidays
- Health insurance
Senior Clinical Trial Manager
Entrada Therapeutics —Boston, MA
- $160,000 - $185,000 a year
- Remote
- 7 years
- Bachelor of Science
- Bachelor's degree
- Disability insurance
- Health insurance
Quick Apply
Senior Clinical Trial Manager (CTM)
Praxis Precision Medicines, Inc. —Remote
- $168,000 - $188,000 a year
- Email
- Remote
- 5 years
- Bachelor's degree
- Contracts
Quick Apply
Clinical Study Manager
IUVO BIOSCIENCE OPERATIONS, LLC —Remote
- $100,000 - $150,000 a year
- Remote
- Microsoft Outlook
- Computer literacy
- Basic math
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Clinical Trial Manager
Fortrea —Remote
- $140,000 - $148,000 a year
- Full-time
- Remote
- English
- 3 years
- Master's degree
Clinical Study Project Manager
IUVO BIOSCIENCE OPERATIONS, LLC —Remote
- $110,000 - $140,000 a year
- Remote
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
Quick Apply
Senior Clinical Trial Manager
Oura —Remote
- $117,300 - $169,000 a year
- Remote
- 5 years
- Travel
- Mentoring
- Paid holidays
- Health insurance
Manager, Clinical Trial Management
Precision for Medicine —Gladstone, NJ
- $133,900 - $200,900 a year
- Online Application
- Remote
- Microsoft Excel
- Microsoft Outlook
- 5 years
Quick Apply
Clinical Trial Manager
Generate Biomedicines —Somerville, MA
- $127,000 - $178,000 a year
- Remote
- Mid-level
- Bachelor's degree
- Travel
17h
Clinical Trial Manager
CareDx, Inc. —Brisbane, CA
- $124,000 - $155,000 a year
- Full-time
- Remote
- Microsoft Excel
- Microsoft Outlook
- Inventory management
- Commuter assistance
- Employee stock purchase plan
Senior Clinical Trial Manager
Katalyst Healthcares & Life Sciences —South Plainfield, NJ
- Contract
- Remote
- Microsoft Outlook
- Computer literacy
- 3 years
Quick Apply
Clinical Trial Manager/Sr Clinical Trial Manager
Erasca —San Diego, CA
- $145,000 - $190,000 a year
- Remote
- Medicine
- Inventory management
- 5 years
- Health savings account
- AD&D insurance
Senior Clinical Project Manager
CG Oncology Inc —Remote
- $149,000 - $175,000 a year
- Full-time
- Remote
- Bachelor's degree
- Mentoring
- Senior level
- Health savings account
- Disability insurance
Quick Apply
Clinical Trial Manager (Retina)
4D Molecular Therapeutics —Emeryville, CA
- $150,000 - $170,000 a year
- Remote
- Microsoft Excel
- 6 years
- Microsoft Outlook
Clinical Project Manager (CRO) - Remote
C&R Research US —Remote
- $130,000 - $155,000 a year
- Part-time
- Remote
- Nursing
- Microsoft Excel
- HIPAA
- Paid time off
- Flexible schedule
Quick Apply
1d

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Clinical Trial Manager

Medilink Therapeutics
Remote

Quick Apply

Job Details

Full-time
$120,000 - $200,000 a year
10 days ago

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Vision insurance
401(k) matching
Flexible schedule
Life insurance
Retirement plan

Qualifications

Microsoft Excel
Team supervision
Bachelor's degree
Project management experience in healthcare
Managing clinical research teams
Vendor relationship management
Leading team collaboration initiatives
Vendor negotiation
Productivity software
Cross-functional team management
Technical Proficiency
Cross-functional communication
Leading research teams

Full Job Description

Clinical Trial Manager–JD

MediLink Therapeutics is seeking an experienced and passionate Clinical Trial Manager to join our growing team. This individual will be responsible for the cross-functional management of project progress aimed at delivering effective and organized Clinical Operations activities by leveraging his or her expertise in mAb/ADC trials. This position is a full-time position based in the United States. Detailed information as following:

KEY DUTIES & RESPONSIBILITIES:

1. The Clinical Trial Manager will be responsible for leading the clinical study planning as well as development and management of study timelines, budget, resources, risk, and quality plans.

2. This role is responsible for collaborative and effective management of cross-functional study team activities, as well as communication with and management of multiple external vendors and stakeholders (e.g., CROs, central labs, IRBs/ECs, and other external partners)

3. S/he proactively identifies, manages, and communicates risks to key stakeholders and is also in communication and closely integrated with clinical trial sites, promoting relationship development with team members, stakeholders, Investigators, and site staff.

4. Coordinate cross-functional activities, leads the activities of the Clinical Trial Working Group, a cross-company and cross functional team, as it relates to study-level strategy, timelines, goals, and quality.

5. Acts as ad hoc member of the Clinical Development Sub-Team to collaborate in the program level development of clinical strategies, goal setting, and establishment of timelines.

6. Evaluates, selects, and ensures appropriate oversight of Contract Research Organizations (CROs) and other external vendors.

7. Builds solid relationships with key counterparts at CRO(s) and other external vendors.

8. Communicates with clinical trial sites as appropriate to ensure optimal Sponsor-Site relationships.

9. Communicates trial status within and outside the study team to ensure cross-functional alignment of expectations, priorities, and deliverables.

10. Provides input to the development of study-level budget(s) and demonstrates accountability for the management of assigned clinical study budget(s)

11. Tracking vendor performance against scopes of work, contracts, and invoices to ensure consistency between work performed and contractual agreement(s)

12. Facilitating review of study-level scopes of work, invoices, change request forms, and change orders to ensure consistency with study progress and/or evolving study needs.

13. Anticipates, recognizes, and manages issues, exhibits the ability to recognize the need to seek assistance from or inform Senior Management of specific risks/issues; understands when decision making can and needs to occur at the study team level versus when there is a need for escalation to the program level or to Senior Management

14. Analyzes clinical study and investigative site risks and implements corrective actions, where required.

15. Drives quality-by-design efforts to proactively identify and manage risks to trial quality and ensure MediLink is always inspection ready. Study Management and Oversight

16. Drives site start-up, subject enrollment, clinical monitoring activities, clinical site compliance and data metrics from CROs, central labs, and other external vendors

17. Leads development and execution of operational activities outlined in various study plans, SOPs, study procedures, etc.

18. Coordinates the development and distribution of critical study documents, including ICFs, operational documents, study reference documents, study newsletters, site materials, and other study related documents; reinforces the development of clinical study protocols, clinical study reports and other documents as needed.

19. Partners with Global Supply Chain (Technical Operations) team to provide oversight of the applicable study drug(s), including supply projections, distribution, labeling and destruction.

20. Tracks clinical study metrics and reports to management on study(ies) run by MediLink partners, as applicable.

21. Plans, facilitates, and monitors training at investigator meeting(s), internal and vendor kick-off meeting(s), and various CRO (or other vendor) meeting(s)

22. Performs quality assurance checks (e.g., reviewing protocols for operational effectiveness, monitoring trip reports for potential gaps in site/CRA training, conducting co-monitoring visits at clinical sites, reviewing data listings at interim analysis milestones)

23. Coordinates Independent Data Monitoring Committees (IDMCs), when applicable, including collecting confidentiality agreements, contracts, and conflict of interest forms from IDMC members, reviewing IDMC Charter, planning and scheduling meeting(s)

24. Supports and collaborates with GCP QA during site selection and site/study audit activities.

25. Leads Clinical Operations preparation of inspection readiness activities for FDA and other applicable regulatory body audits and/or meetings.

26. Provides guidance and shared learning within and across teams.

27. Mentors more junior Clinical Operations staff member(s) Participates in internal and external training programs to ensure skills are learned and maintained.

28. Champions operational best practices and seek opportunities for innovation and efficiencies within the Clinical Operations group.

29. Participates in internal MediLink SOP, WI, and/or template development and review.

30. Performs administrative functions and additional duties as assigned and appropriate

QUALIFICATIONS& REQUIREMENTS:

1. Bachelor’s degree with a life science or healthcare focus or nursing degree required.

2. Highly motivated and proactive self-starter, able to organize and perform complex tasks with minimal supervision.

3. Proven ability to effectively manage and provide oversight of CROs and multiple vendors for complex global protocols.

4. Ability to organize and manage multiple priorities required.

5. Strong team participation and leadership skills, including excellent oral and written communication skills required.

6. Ability to collaborate effectively with the study team, cross functional team members and external partners (including investigator and site staff) using collaborative influence and negotiation skills.

7. Proficiency in Microsoft Word, Excel, and PowerPoint

8. Ability to multitask with significant attention to detail.

9. Ability and willingness to travel up to 20% of the time.

Job Type: Full-time

Pay: $120,000.00 - $200,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Flexible schedule
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Retirement plan
Vision insurance

Work Location: Remote

Quick Apply

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