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Registry Manager

ThermoFisher Scientific

Remote · USJobSeen 1 day agoSeen in employer's feed 1 day ago

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At a glance

Compensation
No compensation found
Location
Remote · US
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

GCP Training Certificate, requiredHSP Training Certificate, required

Job overview

The Registry Manager oversees day-to-day operations at assigned participating sites in a clinical research registry. The role supports protocol execution and regulatory compliance, addresses site concerns and data queries, conducts site initiation and management visits, and maintains registry documentation and performance. The position is remote-based and seeks a candidate with at least four years of clinical research experience, a bachelor’s degree or equivalent experience, and proficiency with specified research platforms.

Skills & qualifications

RequiredNice to have

Skills

MS Office, requiredSalesforce, requiredREDCap Cloud, requiredZelta EDC, requiredGCP, requiredHSP, requiredClear Writing, nice to haveAttention to Detail, nice to haveAccuracy, nice to haveInterpersonal Skills, nice to haveStudy Timeline Management, requiredData Analysis, nice to haveData Interpretation, nice to haveLarge Data Systems, required

Qualifications

Bachelor's or Equivalent Experience, nice to haveAdvanced Degree, nice to haveResearch Certification, nice to haveRegulatory Certification, nice to have4+ Years Clinical Research Experience, requiredGCP Training Certificate, requiredHSP Training Certificate, required

Full job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life – To enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. As part of our clinical research portfolio, our evidence-based solutions specialize in generating data intelligence and clinical insights needed to bring safe and effective treatments to market. Your objectivity and dedication to patient safety will improve health outcomes that people and communities depend on – now and in the future.

Location - Remote Based

As a Registry Manager, you will serve as a key member of the team and will be responsible for the day-to-day operations at assigned participating sites.

A Day in the Life:

  • Works on site problems of moderate scope where analysis of data requires evaluation of identifiable factors. Demonstrates good judgment in selecting methods and techniques for obtaining solutions. Networks with senior internal and external personnel in own area of expertise.

  • Interface with sites participating in assigned registry.

  • Communicate appropriately to registry management all site concerns or issues that may arise.

  • Implement and facilitate protocol execution and regulatory compliance during site initiation and throughout sites participation in the registry.

  • Identify and support site staff with data queries in a timely manner.

  • Conduct SIV and Remote Site Management and Metric Review visits.

  • Maintain registry Master File documentation and performance.

  • Identify and communicate poor performing sites in a timely yet appropriate manner.

  • Provide input to the development of registry timelines, procedures, forms, registry support materials, manuals, and tracking systems as requested by manager.

Keys to Success:

Education:

  • Bachelor’s degree, preferably in life sciences, public health, health services research or related area and or equivalent experience

  • Advanced degree, Research, and regulatory certifications, i.e.., RAPS or ACRP certificates preferred

Experience:

  • 4 + years’ experience in a clinical research setting.

  • Requires knowledge and utilization of MS Office, Salesforce, REDCap Cloud, Zelta EDC platforms.

  • Requires GCP and HSP training certificate per policies and procedures.

Knowledge, Skills, Abilities:

  • Demonstrated ability to write clear and complete assignments with attention to detail and high degree of accuracy. Strong interpersonal skills.

  • Must be able to manage multiple study timelines, sites, and subscriber's commitments.

  • Experience analyzing and interpreting written material and quantitative data to draw conclusions and make recommendations based on that data preferred

  • Demonstrated proficiency in accessing information stored in large data systems.

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Apply today! http://jobs.thermofisher.com

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Accessibility/Disability Access

Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.

*This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

How this job compares

Set against the 1,299 open Clinical Research jobs on Olive Jobs, counted November 15, 2026.

Pay
  • This postingNot listed
  • North Carolina median$82–220K/yr34 salary ranges
  • US median$26–36/hr180 hourly ranges
Openings
Olive Jobs lists 61 open Clinical Research jobs in North Carolina and 1,299 across the US. 10% of them nationwide are listed as remote or flexible.
Hiring the most in North Carolina
Experience
This posting asks for at least 4 years of experience; Clinical Research postings that state a minimum ask for 3 years at the median (1,014 postings).
Education
545 of the 1,299 open Clinical Research jobs (42%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 15, 2026. Figures based on too few postings are left out.

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