New · posted Nov 4
Parexel · Pharmaceuticals
Feasibility Study Manager
- Remote, US
- Remote
- Full-time
- Manager
What you need
Minimum Eligibility Criteria
Education: BA or equivalent
Year of experience: 3-5 years industry related experience
What you'll do
Feasibility Study Manager Core Job Duties
- Adapt draft site feasibility questionnaires into electronic survey platform and format
- Apply appropriate ‘branching’, conditional logic and scoring parameters, as determined by the Feasibility Lead
- Develop necessary survey reporting templates within survey platform or via external systems as necessary
- Conduct appropriate quality checks on potential investigators prior to survey outreach
- Assist in cross-check for available CDAs prior to survey launch
- Responsible for loading identified site list into survey management system and ensuring all planned investigators for contact are loaded into the applicable survey
- Responsible for survey launch and regular monitoring & maintenance of survey preparation and management including:
- Survey Delegation
- Reconciling survey status
- Ensuring notes and details are appropriately documents
- Identification & collation of invalid contact details
- Proactive research and update invalid or missing contact details to ensure seamless outreach and response efforts and tracking
- Responsible for reporting and monitoring of country-level responses to aid in early risk and mitigation planning to ensure survey objectives can be met
- Responsible for execution of agreed site identification strategy, including:
- Ensuring identification of priority site designation is applied
- Application of agreed communication strategy and supporting materials (study summary details, communication templates, designated email origin within survey system)
- Facilitation of revisions to survey content, scoring parameters, and/or site & country list throughout survey duration
- Monitoring status of site CDA negotiations, and disseminating status updates internally as needed
- Responsible for survey closure tasks, including but not limited to site notifications
From the posting
About Parexel
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
REMOTE - US
Equal opportunity, accessibility and legal noticesParexel's statements, word for word
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Job intelligence
The context around this role
Live data · November 4, 2026
Salary intelligence
How the pay compares
Manager roles in the US19 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| All US (middle half) | $150,000 | $154,500 | $161,250 |
Comparisons: the base pay employers published on open Clinical Operations roles at the same level on Regulatory Jobs, November 4, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Operations
The general path across 104 open Clinical Operations roles on Regulatory Jobs, with the titles they carry most. Not Parexel's own promotion track.
Career resources on Clinical Operations
Skills DNA
What this role leans on
How many of the posting's 14 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Investigations and CAPA2
- Clinical trial conduct2
- Collaboration and leadership2
- Documentation and SOPs1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Clinical Operations work in pharmaceuticals, each linked to the agency or standards body that publishes it.
- ICHICH E6(R3) good clinical practice(official source, opens in a new tab)The international standard for the design, conduct and reporting of clinical trials
- FDA21 CFR Part 312(official source, opens in a new tab)Investigational New Drug applications and sponsor duties in drug trials
- FDA21 CFR Part 50(official source, opens in a new tab)Protection of human subjects: informed consent in FDA-regulated trials
- FDA21 CFR Part 56(official source, opens in a new tab)Institutional review boards for FDA-regulated clinical investigations
- EUEU Clinical Trials Regulation 536/2014(official source, opens in a new tab)How clinical trials of medicines are authorized and run in the EU, through CTIS
- ICHICH E8(R1)(official source, opens in a new tab)General considerations for clinical studies and quality by design in trials
- HHS45 CFR Part 46 (Common Rule)(official source, opens in a new tab)The federal policy for the protection of human research subjects
- NIH42 CFR Part 11(official source, opens in a new tab)Clinical trial registration and results reporting on ClinicalTrials.gov
- FDAFDA Bioresearch Monitoring (BIMO)(official source, opens in a new tab)FDA inspections of clinical investigators, sponsors, IRBs and GLP labs
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- HHSHIPAA Privacy Rule(official source, opens in a new tab)Federal protections for individually identifiable health information
- EUGDPR (Regulation 2016/679)(official source, opens in a new tab)The EU General Data Protection Regulation for personal data, including health data
- ICHICH E9 and E9(R1)(official source, opens in a new tab)Statistical principles for clinical trials and estimands
- FDA21 CFR 314.80 and 600.80(official source, opens in a new tab)Postmarketing reporting of adverse drug and biologic experiences
- ICHICH E2A to E2F(official source, opens in a new tab)Clinical safety data management, expedited reporting and periodic safety reports
- ICHMedDRA(official source, opens in a new tab)The ICH medical terminology for coding adverse events and medical history
Company hiring pulse
Parexel on Regulatory Jobs
- 49
- Open roles
- 48
- Distinct roles
- 6
- Locations
By discipline
- Clinical30 61%
- Regulatory18 37%
- Quality1 2%
By level
- Senior & Principal31 63%
- Manager11 22%
- Associate & Specialist6 12%
More roles at Parexel
- View role
Clinical Operations Manager-F - Budgets and Contracts - FSP
Remote, USManagerPharmaceuticalsSalary not listed
- View role
Clinical Research Associate II (US West) - FSP
Remote, USAssociate & SpecialistPharmaceuticalsSalary not listed
- View role
Clinical Study Physician - Oncology - FSP
Remote, USSenior & PrincipalPharmaceuticalsSalary not listed
- View role
Clinical Scientist- FSP
Remote, US SoutheastAssociate & SpecialistPharmaceuticalsSalary not listed
Similar Clinical Operations roles elsewhere
- View role
Manager, Study Start Up
Eikon TherapeuticsJersey City, NJ · HybridManagerPharmaceuticals$130K–$158K
- View role
Associate Manager / Manager, Clinical Operations - FSP
Thermo Fisher ScientificRemote, CaliforniaManagerPharmaceuticals$115K–$180K
- View role
FSP Associate Manager Clinical Operations
Thermo Fisher ScientificRemote, North CarolinaManagerPharmaceuticalsSalary not listed
- View role
Global Study Manager
ICONRemote, USManagerPharmaceuticalsSalary not listed
Feasibility Study Manager at Parexel
Open until filled.