Senior CTM Job at Solomon Page (South San Francisco)

Senior Clinical Trial Manager

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

South Korea , Seoul

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization
Bachelor's degree in health, life sciences, or other relevant fields of study
At least 10+ years of relevant experience in clinical trial management
Experience in managing complex or global trials is advantageous
Preferred: Experience in managing all trial components from start-up to database lock
Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives
Fluency in English (reading, writing, speaking)

Job Responsibility

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

What we offer

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, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others

Fulltime

Senior CTM (Phase 1)

A South San Francisco based pharmaceutical company is looking for a Contract Sen...

Location

United States

Salary:

Not provided

Solomon Page

Expiration Date

Until further notice

Requirements

Minimum Bachelor’s degree in a relevant scientific discipline
Minimum 7 years of pharma or biotech industry experience managing clinical trials
Sponsor experience required
Global Phase I experience required
US and Global experience required
CRO & Vendor Management experience required

Job Responsibility

Lead global cross-functional study teams through all study stages
Provide support and contribute to RFP/RFI process, analyze service providers, budgets/proposals, conduct bid defense meetings, award services, negotiate and execute complex agreements (i.e., CRO, study related collaboration agreements)
Manage CRO and service providers
Assist with Inspection Readiness activities
Manage clinical study timelines with PM Team
Develop study documents such as CRF design, project plans, Service Provider Oversight plans
Manages study sites and study related activities (site selection, start up, recruitment, enrollment, study management, monitoring report review, and more)
Provide regular updates to Study lead and other stakeholders
Proactively identify, manage, or escalate issues appropriately
Work with Finance to manage budget for studies and vendors

What we offer

medical
dental
vision
401(k)
telehealth services
ESOP
commuter benefits

Senior Clinical Trial Manager

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

Mexico , Mexico City

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

A minimum of 5 years of experience as a Senior Clinical Trial Manager, ideally having progressed through CTM I and CTM II, for a total of 7+ years of CTM experience
Strong experience managing North America and Canada, including: ICF creation
Advarra IRB
Local IRB management
Canada MOH submissions
Demonstrated experience managing LATAM studies end-to-end, from Start-Up through Close-Out
Excellent English proficiency (reading, writing, and speaking)
Bachelor’s degree in health, life sciences, or another relevant field

Job Responsibility

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

What we offer

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, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others

Fixed Income Securities Middle Office

Step into the role of Fixed Income Securities Middle Office at Barclays, where y...

Location

India , Pune

Salary:

Not provided

Barclays

Expiration Date

Until further notice

Requirements

Knowledge of electronic platforms for trading and confirmations including Bloomberg, TradeWeb, MarketAxess, Omgeo CTM and FIX
Client service experience – understand the needs of clients and how to manage client expectations
Degree educated or equivalent qualification
Preferably having experience in supporting Fixed Income products
Strong understanding of the end-to-end process flows and the control points along the process chain
Proficient in Microsoft Office products
Good verbal and written communication skills
Strong team player, self-starter with positive attitude
Able to work in a fast-paced environment, meet tight deadlines with a good sense of urgency and accountability
In-depth technical knowledge and experience in their assigned area of expertise

Job Responsibility

Provide first-class support by conducting in-depth due diligence
Ensure compliance with regulatory requirements
Safeguard our clients and organization with expertise and care
Ensure that the data flowing through the Barclays IB infrastructure is complete, timely and well controlled
Provide strong client support for Fixed Income confirmations to ensure smooth confirmation of trades in CTM
Liaise with clients in a timely manner to ensure trade are allocated and settled on time
Ensure exception management is complete within two internal systems
Onboard clients as well as general query resolution
Support business areas with day-to-day processing, reviewing, reporting, trading and issue resolution
Support various business areas with day-to-day initiatives including processing, reviewing, reporting, trading, and issue resolution

What we offer

Hybrid working
Structured approach to hybrid working with fixed 'anchor' days
Supportive and inclusive culture and environment
Opportunities to innovate, collaborate, and deliver great outcomes
Welcoming and inclusive culture supports you to bring your whole self to work
State-of-the-art technology hub
Excellent facilities for work, socialising and leisure

Fulltime

Senior Cloud Engineer

Be a part of our passionate and determined team that is on a mission to use our ...

Location

United States , Huntsville

Salary:

130000.00 - 136000.00 USD / Year

Banner Defense

Expiration Date

Until further notice

Requirements

US Citizenship
Active Secret Clearance, with ability to obtain a Top-Secret clearance
Master's Degree
12+ years of relevant experience
AWS Foundational and Associate level certifications and/or Azure Fundamentals and Associate level certifications
Knowledge of model and simulation (M&S) development
Experience in Agile and Lean software development principles
Experience with Artificial Intelligence (AI) and Machine Learning (ML) concepts and applications
Experience in software containerization development concepts and applications
Experience in model and simulation requirements development

Job Responsibility

Develop and review Framework Software in the Cloud (SWIC) requirements
Develop and review Framework and Missile Defense System Interface Control Documents (ICD), to include Objective Simulation Framework (OSF) Ground Test Integrated System Simulation (GTISS)
Lead and facilitate technical discussions and collaboration activities with both internal and external stakeholders to include Prime Contractors and the Missile Defense elements
Actively participate in Framework, RepBox and CTM Program Agile Software Development Increment Planning activities
Draft and review technical documents, briefings, white papers, etc.
Play a role in overall functional strategic planning of Framework, RepBox and CTM Systems Engineering (SE) processes within the organization

What we offer

Medical (employer paid 80%)
Dental (employer paid 100%)
Vision (employer paid 100%)
401k (with generous matching)
Profit Sharing
Tuition Refund
Paid Holidays
Rewards and recognition
Family-friendly environment
Professional growth opportunities

Fulltime

Security Tower Lead

HPE Operations is our innovative IT services organization. It provides the exper...

Location

India , Bangalore

Salary:

Not provided

Hewlett Packard Enterprise

Expiration Date

Until further notice

Requirements

BE/ B.Tech/ M.Tech/ MSc/ MCA qualification or equivalent
Should have at least one certification out of the following: CCIE-Security, CISSP, CISA, CISM, CCSP, CCNP-Security, GIAC
Minimum 12 years of IT experience covering the following: Network Security exp – 8 Yrs
Handson experience in Network Security Device - Firewall, Load Balancer, DDoS, IPS/IDS, WAF, Deception Technology, APT
Handson experience in Infrastructure Vulnerability assessment, Threat modelling
Clear understanding on Risk management
Experience in security infrastructure components
Tools – Algosec or Tufin, Checkpoint Harmony and Maestro

Job Responsibility

Exposure in leading end to end Project delivery ensuring noise free delivery with zero escalation
Experience in facing senior management and present the solution and outcome
Experience in advising senior management on security strategies and implementation plans at the organization ecosystem level with ROSI analysis
Experience in consulting on governance, strategy and transformation
Experience in consulting on analysing and managing risks and provide remediation methodologies
Experience in leading complex IS project and handle cross functional team
Experience in driving key meetings for closing identified IS issues and gaps across different teams and vendors and achieve the outcomes within the define deadline
Experience in using open sources tools and technologies and managing risks and vulnerabilities across the same
Experience in automation of workflows, processes using automation tools and scripts
Knowledge in AI & ML security

What we offer

Health & Wellbeing
Personal & Professional Development
Unconditional Inclusion

Fulltime

Mobilisation Coordinator Site

The Site Mobilisation Coordinator is responsible for delivering efficient and ac...

Location

Australia , Perth

Salary:

Not provided

PLS

Expiration Date

Until further notice

Requirements

Current C class driver's license
High efficiency using the full Microsoft Office suite
Minimum of 1 year of INX experience specifically within the InFlight and +Process applications
Minimum of 1 year experience within a site mobilisation role
Excellent customer service skills
Previous experience in a similar role
General understanding of mining operations and requirements
Strong administration background
Ability to meet deadlines and timeframes
Ability to work in a busy environment and under pressure

Job Responsibility

Coordinate all site mobilisations and site-based travel requirements, including the onboarding of new employees and contractor personnel
Manage all charter and commercial flight bookings, waitlists, rosters, and accommodation requirements using Corporate Travel Management (CTM)
Create traveller profiles, validate & verify completion of site entry requirements, and ensure all mobilisation documentation is completed accurately
Prepare and distribute daily and weekly charter manifests
Coordinate ground transport including bus services
Assist with the organisation of additional charter flights when required
Provide timely and accurate turnaround of all contractor travel requests
Assist with coordination of travel requirements for Perth office personnel attending site
Maintain and update employee and contractor records in INX InFlight, INX InTuition, and INX +Process, ensuring system integrity and compliance
Create and maintain site rosters, including coordination and management of FIFO & DIDO travel and rosters

What we offer

Access to newly refurbished facilities at Pilgangoora, including gym, tennis, pickleball and volleyball courts, sports oval and scenic walking tracks
Health and wellbeing allowance
Paid community leave
Monthly employee recognition awards
Access to PLS’ KidsCo School Holiday Program
Access to our Employee Assistance Program and Company Chaplains

Fulltime

Senior In-House Clinical Research Associate

The Senior In-House Clinical Research Associate (CRA) supports the planning, exe...

Location

United States , Philadelphia

Salary:

Not provided

Cabaletta Bio Inc

Expiration Date

Until further notice

Requirements

A bachelor's or master's degree in a relevant field, such as life sciences, nursing, or pharmacy
At least 2-3 years of experience in clinical research, preferably in a CRA or related role
Experience with all aspects of trial and site startup and vendor selection and management, study management, and monitoring
Strong knowledge of clinical trial conduct, GCP, FDA regulations, and ICH guidelines
Excellent written and verbal communication skills to effectively communicate with study sites, investigators, and internal study team members
Strong organizational skills to manage multiple tasks and priorities simultaneously
Strong attention to detail to ensure accurate and complete data collection and documentation
Proficiency in Microsoft Office applications and experience working with electronic data capture systems (EDC)
Ability to build positive relationships with study sites and investigators
Flexibility to adapt to changing project needs and timelines

Job Responsibility

Provide monitoring oversight by reviewing monitoring reports and escalate any trends with respect to data quality or study conduct to the appropriate CTM, Clinical Operations
Perform clinical research site activities, such as onsite or remote co-monitoring, training, motivational, and sponsor oversight visits, as needed
Support the oversight of activities of CRO and study vendors to ensure compliance with the study protocol and on-time achievement of overall clinical objectives and deliverables
Contribute to the development of study documentation including protocol review, creating study manuals, ICFs, study plans and CRFs. Contribute to study start-up activities including site selection
Support the Clinical Operations team and cross-functional representatives as required in relationship management tasks (e.g., study logistics, patient enrollment, safety, data management, etc.) to accurately coordinate clinical study activities
Ensure that study documentation is maintained according to applicable regulations, industry accepted standards, and SOPs that govern clinical studies
Collaborate with Clinical, Regulatory, and Quality team members to ensure compliance of study activities
Identify and resolve study-related issues and deviations
Communicate with study sites and investigators
Provide support to study sites, including training and troubleshooting

What we offer

health and retirement, PTO, and stock option plans

Senior CTM

Solomon Page

Location:
United States , South San Francisco

Category:
-

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 30, 2026

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