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Associate Data Scientist
Schumacher Operations Inc
Canton, OH
The Associate Data Scientist applies data science to marketing, reporting directly to the Head of Data Science. The role covers marketing activity and attribution, the customer journey from…
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Relationship Banker II - Arnold
Regions Bank
Arnold, MO
…interested in beginning a career with opportunities for growth, development, and upward…
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Electrical Process Controls Technician
MLC
Sainte Genevieve, MO
Job Title: Electrical Process Controls Technician
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Team Lead/Charge Nurse ICU Nights
BJC HealthCare
Saint Peters, MO
- $36.25 to $58.01 USD / hour
The BJC RN Career Ladder promotes professional development, leadership, collaboration, education and service excellence and gives staff the opportunity to continue doing what they do best -…
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Registered Nurse - Cardiac Catheterization/Electrophysiology Laboratory Nurse
Veterans Affairs, Veterans Health Administration
Columbia, MO
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Oracle Fusion Manufacturing Senior Manager - Pharmaceutical
Accenture
St. Louis, MO
- $122,700 to $302,400 USD / year
…the future and bring it to life using design thinking, agile development methodologies, and new smart tech like IoT, automation, and AI. We even built our own platform, myConcerto, that…
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Threat Informed Defense Senior Manager
Accenture
St. Louis, MO
- $132,500 to $338,300 USD / year
Telemetry pipeline integration and threat hunt program development across EDR, network, identity, cloud, and OT data sources.
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Assistant Nurse Manager- Med/ Surg
Veterans Affairs, Veterans Health Administration
Saint Louis, MO
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Neuro ICU Clinical Nurse Manager
BJC HealthCare
Saint Louis, MO
- $92,248 to $152,318.4 USD / year
…outcomes. This role leads nursing staff, supports professional development, manages daily unit operations, and collaborates with interdisciplinary teams to drive quality, patient safety,…
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Med-Surg RN – Regional Float Long Term Assignment (Nights) – CSO
BJC HealthCare
Saint Louis, MO
- $34 to $42.5 USD / hour
…effective relationships and serves as an advocate to facilitate the development of the care plan unique to the patient’s care needs. Uses the nursing process and evidence based practice to…
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Cardiac Sonographer Reg (RDCS) - Christian Hospital
BJC HealthCare
Saint Louis, MO
- $38.62 to $57.93 USD / hour
Associate's Degree or Trade School equivalency
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BH
Lab Associate III - Floater
BJC HealthCare
Saint Louis, MO
- $18 to $27.35 USD / hour
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Medical ICU Clinical Nurse Manager
BJC HealthCare
Saint Louis, MO
- $92,248 to $152,318.4 USD / year
…outcomes. This role leads nursing staff, supports professional development, manages daily unit operations, and collaborates with interdisciplinary teams to drive quality, patient safety,…
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BH
Charge MRI OR Scrub Radiology Technologist - 3 Days per Week!
BJC HealthCare
Saint Louis, MO
- $37.08 to $55.61 USD / hour
Next Steps: If selected to move forward with Interview Process, a Talent Advisor will contact you via email for a screen
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CT Technologist (Day) 3 Days per Week - Christian Hospital
BJC HealthCare
Saint Louis, MO
- $33 to $49.5 USD / hour
If selected to move forward with Interview Process, a Talent Advisor will contact you via email for a screen
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Senior Oncology Data Specialist
Ascension Health
Saint Louis, MO
Maintain the long-term follow up process of data collection and input for all cancer registry patients.
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Construction Project Manager
Ascension Health
Saint Louis, MO
Project Mgmt Professional. Certified Associate in Project Management (CAPM) or Project Management Professional (PMP) accepted.
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Cash Operations Business Partner
Waste Harmonics Keter
Stamford, CT
Spot recurring payment issues and find ways to make the process more accurate or faster
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Associate Director, Omnichannel Therapeutic Area Lead
Otsuka America Pharmaceutical Inc.
Jefferson City, MO
Serve as a strategic thought partner to Brand, Medical, and Commercial leadership, contributing to the development of customer engagement strategy and plans informed by deep customer…
Added 1 min ago
Senior Learning Design Professional
Humana
Jefferson City, MO
…theory to determine the appropriate learning solution for a new process or system, or to address a knowledge or performance…
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Platform Engineer - Remote
SitusAMC
Jefferson City, MO
Develop and maintain the in-house CI/CD automation pipeline as an individual contributor on the Cloud development platform team.
Added 1 min ago
Senior Director, Global Clinical Development Psychiatry and Neurology
Otsuka America Pharmaceutical Inc.
Jefferson City, MO
-Within Otsuka Pharmaceutical Co. exists Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC) a U.S.A. subsidiary exists the Global Clinical Development (GCD) department.…
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Sales Associate
Orangetheory - Franchise #0320
AUSTIN, TX
- $15 USD / hour
The Sales Associate is responsible for supporting front-line studio operations and delivering an exceptional member experience at every interaction within AFG HoldCo studios. This role…
Added 1 min ago
O-
Sales Associate
Orangetheory - Franchise #0320
AUSTIN, TX
- $15 USD / hour
The Sales Associate is responsible for supporting front-line studio operations and delivering an exceptional member experience at every interaction within AFG HoldCo studios. This role…
Added 1 min ago
Entry Level technician
Hendrick Automotive Company
Kansas City, MO

PPD Development, LP

FSP Sr CRA I

Remote, United States

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Job details

Experience: Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 3+ years).
Posting language: English
Posted: Nov 5, 2026

Original job description

Work Schedule Standard (Mon-Fri) Environmental Conditions Office

Job Description

Join Us as Senior Clinical Research Associate I – Make an Impact at the Forefront of Innovation. We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. DESCRIPTION As a Senior Clinical Research Associate I in our FSP model, you will be dedicated to one specific client, acting as a representative of the client while exercising strong communication and collaboration skills. You will perform and coordinate all aspects of the clinical monitoring and site management process. You will conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will act as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites.

What You'll Do:

Monitors investigator sites with a risk-based monitoring approach.
Applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks.
Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities.
Assess investigational product through physical inventory and records review.
Documents observations in reports and letters in a timely manner using approved business writing standards.
Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution.
Maintains regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
Conducts monitoring tasks in accordance with the approved monitoring plan.
Participates in the investigator payment process.
Ensures a shared responsibility with other project team members on issues/findings resolution.
Investigates and follows-up on findings as applicable.
Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required.
Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS).
Performs QC check of reports generated from CTMS system where required.
Participates in investigator meetings as necessary.
Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites.
Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted.
Ensures trial close out and retrieval of trial materials.
Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations.
Conducts on-site file reviews as per project specifications.
Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members.
Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc).
Facilitates effective communication between investigative sites, the client company and the project team through written, oral and/or electronic contacts.
Responds to company, client and applicable regulatory requirements/audits/inspections.
Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.
Contributes to other project work and initiatives for process improvement, as required.

REQUIREMENTS

Education and Experience Requirements:

Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 3+ years).
Oncology experience preferred.

Knowledge, Skills and Abilities:

A seasoned, experienced professional, with a full understanding of area of specialization; resolves a wide range of issues in creative ways.
Strong critical thinking and problem-solving skills.
Excellent clinical trials monitoring skills; remote and on-site.
Demonstrated understanding of ICH-GCP guidelines, applicable regulations and SOPs.
Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors.
Demonstrates good judgement in selecting methods and techniques for obtaining solutions.
Strong communication and collaboration skills with ability to interact effectively with investigative sites, clients, and internal teams.
Ability to act as a representative of the client while maintaining professional relationships.
Advanced written and oral communication skills.
Strong organizational skills and attention to detail.
Demonstrated use of computer systems including CTMS and other trial management platforms.
Ability to travel >75% as required for site monitoring activities.

Why Join Us? When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You'll work in an environment where collaboration and development are part of the everyday experience - and where your contributions truly make a difference. Apply today to help us deliver tomorrow's breakthroughs.

Compensation and Benefits The salary range estimated for this position based in Colorado is $90,000.00–$113,000.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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More about this job

Skills

Clinical research
Clinical trials
Communication skills
Collaboration
Regulatory compliance
Documentation
Google Cloud
Root cause analysis
Critical thinking
Problem solving
Monitor activities
Inspection
Process improvement
Organizational skills
Attention to detail

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