Contract CRA Job at Solomon Page (Covington)

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Contract CRA

We are seeking an experienced and highly motivated Clinical Research Associate (...

Location

United States , Covington

Salary:

90.00 - 100.00 USD / Hour

Solomon Page

Expiration Date

Until further notice

Requirements

Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field
Minimum 5 years of Clinical Research Associate (CRA) experience
Direct monitoring experience in pulmonary transplant and/or lung transplant clinical studies is required
Strong understanding of ICH-GCP, FDA regulations, and clinical trial processes
Experience managing high-performing academic medical center sites
Excellent organizational, communication, and problem-solving skills
Ability to travel regularly to assigned study sites

What we offer

medical
dental
401(k)
direct deposit
commuter benefits

Payroll And Benefits Specialist - Contract

Are you a detail-oriented professional with a passion for precision? We are look...

Location

Canada , Winnipeg

Salary:

Not provided

Randstad

Expiration Date

July 23, 2026

Requirements

Degree or diploma in accounting
Strong organizational skills to manage multiple deadlines and high-volume data entry
Proficiency in Microsoft Office application and payroll software (ADP, QuickBooks, Payworks or similar)
Strong analytical skills with the ability to identify and resolve complex payroll discrepancies
Excellent communication skills, with the ability to explain complex benefits information clearly to employees

Job Responsibility

Processing bi-weekly salaried and hourly full-cycle payroll for all employees in an accurate and timely manner
Administer and maintain employee benefits programs, including extended health, dental, and retirement savings plans
Calculating, verifying, and processing statutory deductions, garnishments, and remittances to CRA, WCB, and other government agencies
Process new hires, terminations, salary adjustments, and taxable benefits with a high degree of accuracy
Act as the primary point of contact for employee inquiries regarding pay, benefits, and leave management
Serving as the primary point of contact for all employee questions regarding payroll, compensation, and benefits, providing clear and helpful responses
Manage the year-end process, including the preparation and filing of T4s and other required statutory returns

What we offer

Competitive compensation package for the Winnipeg Market
Experience working in a professional finance & accounting and HR environment
Join a well-respected and leading company within the vibrant retail sector
Become part of a supportive and collaborative in office environment
Access to opportunities for continuous learning and professional development to advance your career in human resources and payroll

Site Care Partner

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

United States

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
Must demonstrate good computer skills and be able to embrace new technologies
Good communication, presentation, and interpersonal skills
Ability to manage required travel
Demonstrated networking and relationship building skills
Demonstrated ability to manage cross functional relationships
Ability to communicate effectively and appropriately with internal & external stakeholders
Ability to adapt to changing technologies and processes
Knowledge of country requirements for GCP that may be different to those of client procedures
Effectively overcoming barriers encountered during the implementation of new processes and systems

Job Responsibility

Site start-up and activation
Deploys client site strategies by qualifying and activating assigned sites
Supports processes to optimize country & site selection activities including review and assessment of the draft potential site list and provide site qualification output for site selection
Collaborates with key stakeholders providing country/regional level input to country outreach surveys including protocol feasibility, country Standard of Care (SOC) and medical practices (as applicable) under supervision
Maintains a knowledge of assigned protocols
Conducts study start-up activities at the site level including but not limited to Site Qualification, coordination of site activation checklist items, Informed Consent Form (ICF) finalization, Site Initiation Visit (SIV) as applicable, including management of issues that may compromise time to site activation
Ensures all the site initiation activity including training per site activation checklist, collect and / complete necessary documentation/ systems needed for site activation
Supports country specific ICF review and deployment up to Site Activation
Ensures follow up activities’ completion post Site qualification visit and SIV to ensure site readiness for First Subject First Visit (FSFV)
Partners with Clinical Research Associate (CRA) to ensure site monitoring readiness in anticipation of FSFV

What we offer

Flexible work arrangements
Career growth and development
Supportive and inclusive environment
Patient-focused
Diverse therapeutic areas and project exposure
Advanced Technology

Fulltime

Senior Clinical Research Associate

Senior Clinical Research Associate - Oncology - East Coast. ICON plc is a world-...

Location

United States , Atlanta; Texas; Maryland; Missouri; Tennessee; North Carolina; Illinois; Ohio; Florida; Philadelphia, PA

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

An undergraduate degree or it’s equivalent in clinical, science, or health related field from an accredited institution
a licensed health care professional (i.e. registered nurse) or equivalent work experience required
5+ years clinical monitoring experience required (Sr CRA)
Knowledge of ICH and local regulatory authority regulations regarding drug
Read, write and speak fluent English
Oncology monitoring experience required
Experience doing feasibility/site selection/site start up required
To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status

Job Responsibility

Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and Internation Conference on Harmonization (ICH) Good Clinical Practice (GCP) guidelines
Assesses the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of clinical trials, and closes clinical trials at investigative sites
Responsible for site startup activities for assigned sites, including but not limited to regulatory documents collection, informed consent review, IRB/IEC submission support, and budgets and contracts negotiations
Reviews and verifies accuracy of clinical trial data collected, either onsite or remotely
Provides regular site status information to team members, trial management, and updates trial management tools
Completes monitoring activity documents as required by sponsor's SOPs
Works closely with other clinical team members to facilitate timely resolution of trial and/or clinical issues
Escalates site and trial related issues per Sponsor's SOPs until identified issues are resolved or closed
Performs essential document site file reconciliation
Performs source document verification and query resolution

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

Senior Grant Administrator

The Senior Grant Administrator, DISC Pre-Award facilitates and supports departme...

Location

United States , Waltham

Salary:

79700.00 - 88800.00 USD / Year

Brandeis University

Expiration Date

Until further notice

Requirements

Bachelor’s Degree required, master’s degree preferred
5-8+ years of related work experience
Experience and demonstrated expertise in a university setting, and deep familiarity with the research administration function, including sponsored projects administration and policy or a related field involving regulatory work and application preparation (i.e. banking, science, etc.)
Understanding of Federal funding agencies and regulatory bodies, and experience in developing approaches to emerging administrative and compliance requirements
Demonstrated ability to manage ambiguity and be able to juggle and prioritize multiple time-sensitive demands in a rapidly changing organization and environment
A collaborative and inclusive professional style, ability to build strategic relationships with staff at all levels, excellent organizational and communication skills (written, verbal, listening), ability to make strategic connections, and utmost respect for discretion, confidentiality and professionalism
Broad and deep knowledge and perspective of the University including academic and central administrative functions
Ability and inclination to anticipate future opportunities and consequences
Resonance with the mission and goals of the Office’s priorities
Certification in Research Administration field [e.g., Certified Research Administrator (CRA®) or Certified Pre-Award Administrator (CPRA®)] required, or ability to obtain within 1 year of start date, or Advanced Degree

Job Responsibility

Pre-Award Proposal Development (90%): Independently supports a portfolio of sponsored projects proposals (typically the more complicated or larger solicitations, including NIH Training grants) and ensures a high-quality product is delivered to the Pre-Award Services team within the ORA including assisting in the development, preparation, finalization, and submission of the proposals prepared by the DISC Office to the Office of Research Administration Pre-Award Team of the grant and contract proposals
Obtains and reviews sponsor guidelines for all proposals
advises the PI on administrative requirements in preparing proposal submissions
Coordinates and reviews certain proposal elements (biosketches and facilities & resources) for consistency, accuracy, and completeness
Reviews proposals for consistency with sponsor guidelines on format, compliance with the FOA, font size and page limits, narrative, etc
Works closely with the PI to develop budgets and budget justification, ensuring accuracy
Reviews budgets for consistency with sponsor requirements
monitors for compliance with agency and University guidelines
verifies all financial information, including institutional salaries, fringe, indirect rates, etc. for the project
Ensures all applications meet sponsor and institutional guidelines and deadlines, including management of the Just-In-Time process

What we offer

medical, dental and life insurance
tuition benefits for employees, dependents and spouses
403b retirement savings plan includes a generous match
free parking
access to a top-of-the-line athletic facility

Fulltime

Site Care Partner II

The Site Care Partneris a key Pfizer point of contact for investigative sites th...

Location

Taiwan , Taipei

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience (estimate at least 7 years’ experience)
Proficiency in local language preferred. English is required
Work as SCP I experience above 2 years
Demonstrated experience in site management with prior experience as a CRA/ Site monitor
Demonstrated experience in start up activities through to site activation
Demonstrated experience in conduct and close out activities
Demonstrated knowledge of quality and regulatory requirements in applicable countries
Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
Must demonstrate good computer skills and be able to embrace new technologies
Excellent communication, presentation and interpersonal skills

Job Responsibility

Accountable for site start-up and activation
Deploy GSSO site strategies by qualifying and activating assigned sites
Supports processes to optimize country & site selection activities including review and assessment of the draft potential site list & provide PTA output for site selection
Supports the Feasibility Strategy and Analytics Lead to ensure that high quality feasibility results are delivered
Collaborate with key stakeholders providing country/regional level input to country outreach surveys including protocol feasibility, country SOC and medical practices (as applicable)
Provide country/regional level input to country strategy, feasibility and protocol design in collaboration with relevant Medical Affairs colleagues, and with input from external clinical experts as required
Maintain a knowledge of assigned protocols
Conduct study start up activities at the site level including but not limited to PTA, coordination of site activation checklist items, ICD finalization, SIV (as applicable), including management of issues that may compromise time to site activation
Ensure all the site initiation activity including training per site activation checklist, collect and / complete necessary documentation/ systems needed for site activation. (e.g. PSR, SART, ESRA, SAC, FU Letter, Planisware, ISF/eISF etc.)
Support country specific ICD review and deployment when applicable

Fulltime

Clinical Trial Oversight Manager

Do more with the knowledge you’re working hard to acquire and the passion you al...

Location

Italy , Milan

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree OR Doctorate degree OR BA/BS/BSc or qualified nurse (RN)
Work experience in life sciences or medically related field, including Biopharmaceutical clinical research experience (clinical research obtained working on clinical trials in a biotech, pharmaceutical or CRO company, or other relevant clinical setting)
Broad work experience working in life sciences or medically related field, including clinical site management experience, obtained working on clinical trials in a biotech, pharmaceutical or CRO company
Experience as a CRA, CTA, and/or Clinical/Regional Manager in the biopharmaceutical industry
Experience in a project leadership role
Experience working with or for Functional Service Provider or Contract Research Organizations
Supervisory Experience
Knowledge of or work experience with a biopharmaceutical GRDCA or QC department
Familiarity with advanced concepts of clinical research, extensive knowledge of ICH/GCP regulations and guidelines, strong knowledge of clinical trial operations, and understanding of Functional Service Provider operational model
Computer and system operation skills

Job Responsibility

Perform sponsor oversight activities of SM-FSP, including staff performance (KPIs, report(s) metric analysis/review), to ensure quality and delivery of Amgen clinical trials
Collaborate closely with SM-FSP Line Manager (FSPLM) to ensure appropriate level of their staff oversight is deployed
Support SM-FSP staff onboarding and training
Be a point of escalation for all stakeholders to support resolution of issues on quality, staff turnover and performance concerns
Work with SM-FSP vendor(s) to ensure timely and appropriate planning, resource and capacity management from study start up to close-out
Conduct on-site quality visits with CRAs where/when appropriate and supports the maintenance of Amgen investigator site relationships
Support inspection readiness, local country and site level audits and regulatory inspections when applicable including CAPA resolution
Organize and lead the Functional Management Team (FMT) Meetings and any other country-level project review meetings, if applicable
Be involved in local and global site management and cross functional stakeholder collaboration
Actively participate in role forums including local and global functional and cross-functional initiatives

What we offer

Full support and career-development resources to expand your skills, enhance your expertise, and maximize your potential along your career journey
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act

Fulltime

CRA, Study Start-up and Maintenance

Specializing in oncology, Kapadi excels at navigating the early stages of drug d...

Location

Poland , Cała Polska

Salary:

Not provided

GRUPA NEUCA

Expiration Date

Until further notice

Requirements

proven 5+ years of experience in study start-up processes in clinical research
a medical-related university degree
working knowledge of ICH-GCP and local regulatory guidelines
strong communication, organizational, and multitasking skills

Job Responsibility

site and project coordination: act as the main point of contact for clinical sites throughout the study lifecycle, providing support for site initiation, compliance, and regulatory documentation
documentation & tracking: maintain and update project documentation, tracking activities, site status, and action items according to SOPs
regulatory maintenance: oversee regulatory updates, including protocol amendments, safety reports, and IRB/IEC submissions, ensuring all documentation is current and compliant
training & compliance: complete required training and keep up-to-date with ICH-GCP guidelines and relevant local regulations
budget and contract: oversight and liaison between site and sponsor with budget and contracts

What we offer

remote work opportunities
professional development in a well‑established company with a strong market position
employment in a company awarded the Top Employer 2026 certificate – we create a work environment based on trust, collaboration, and diversity
a comprehensive benefits package in the form of a cafeteria system – you decide which benefits best suit your needs
Private medical care
Free legal advice
Social benefits
Employee referral program
Day off on birthday
Life insurance

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Contract CRA

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Contract CRA

Contract CRA

Payroll And Benefits Specialist - Contract

Site Care Partner

Senior Clinical Research Associate

Senior Grant Administrator

Site Care Partner II

Clinical Trial Oversight Manager

CRA, Study Start-up and Maintenance

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