Apply to Join Our Clinical Research Talent Network
Submit your application below to be considered for contract and permanent opportunities supporting leading sponsors and CROs.
Personal Information
Name
*
First Name
Last Name
Email
*
example@example.com
Phone Number
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Please enter a valid phone number.
Format: (000) 000-0000.
LinkedIn Profile URL
Location
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Street Address
Street Address Line 2
City
State / Province
Postal / Zip Code
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Your Preferences
Help us understand your preferred role types, work arrangements, and availability so we can align opportunities with your goals.
Interested in: Contract, Permanent, or Both?
*
Please Select
Contract
Permanent
Both
Work Environment Preference
Open to Remote Work
Open to Hybrid Work (Remote + Onsite)
Open to Onsite Work Only
Willingness to Travel (%)
Please Select
0% (No Travel)
Up to 25%
Up to 50%
Up to 75%
75–100% (Frequent Travel)
Select the maximum amount of travel you are willing to consider. This information is optional and may be role-specific.
Geographic Work Authorization
Authorized to work in United States
Authorized to work in Canada
Authorized to work in European Union
Authorized to work in South Africa
Other
Available Start Date
*
-
Month
-
Day
Year
Date
Desired Work Type
*
Please Select
Remote
Onsite
Hybrid
Open
Preferred Functional Area
*
CRA (Clinical Research Associate / Site Monitor)
CTM/CPM (Clinical Trial Manager / Clinical Project Manager)
TMF Management / Trial Master File Oversight
Clinical Data Management
Biostatistics / Biometrics
Pharmacovigilance / Drug Safety (PV Associates, Drug Safety Physicians, Medical Monitors)
Regulatory Affairs / Regulatory Operations
Patient Recruitment & Retention
Other
Role Types of Interest
*
ex: CRA, CTM, PV Associate
Geographic Flexibility
*
Local
Regional
National
Canada
Puerto Rico
Other
How Were You Referred to Us?
Please Select
LinkedIn
ClinDev Global Website
Referral from a Friend or Colleague
Social Media (other than LinkedIn)
Job Board (please specify)
ClinDev Global Outreach (email, recruiter call, etc.)
Let us know how you found us. This information helps us improve outreach and engagement. Optional.
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Professional Background
Tell us about your clinical research experience, therapeutic expertise, and system proficiencies to help us better align opportunities with your skills.
Years of Clinical Research Experience
*
Please Select
0–1
2–5
6–10
>10
Current Employment Status
Please Select
Employed Full-Time
Employed Part-Time
Contract / Freelance
Not Currently Working
Other
Select your current employment situation. This information helps us better understand your availability.
Therapeutic and Specialty Area Experience
*
Rows
Years of Experience (e.g., 5)
Most Recent Year of Experience (e.g., 2022)
Oncology (Solid Tumors)
Oncology (Hematologic Malignancies)
Oncology Immunotherapy (IO)
Rare Oncology
Rare Disease
Orphan Drug Trials
Gene Therapy
Cell Therapy (including CAR-T)
Neurology (including Alzheimer's Disease, Parkinson's Disease)
Pain Management
Cardiology (including Heart Failure, Rare Cardiac Diseases)
Infectious Diseases (including COVID-19, HIV, RSV)
Hematology (non-oncologic)
Immunology (including Autoimmune Diseases)
Endocrinology (including Diabetes, Obesity, NASH)
Gastroenterology (including IBD, Crohn's, Ulcerative Colitis)
Pulmonology (including Asthma, COPD, IPF)
Psychiatry (including Depression, Schizophrenia)
Women's Health (including Endometriosis, Fibroids)
Vaccines
Musculoskeletal Disorders (e.g., Osteoarthritis, Osteoporosis)
Urology (e.g., Overactive Bladder, Prostate Disorders)
Dermatology (including Atopic Dermatitis, Psoriasis)
Ophthalmology (including Wet AMD, Retinitis Pigmentosa)
Mental Health and Addiction Medicine
Nephrology (e.g., CKD, Dialysis)
Hemophilia and Bleeding Disorders
Transplant Medicine (Kidney, Heart, Lung, Liver)
First-in-Human / Early Phase Trials
Adaptive Trial Designs
Master Protocol Trials (Basket, Umbrella, Platform)
Decentralized Clinical Trials (DCTs)
Therapeutic Medical Devices (e.g., Stents, Neurostimulators)
Diagnostic Devices (e.g., Imaging, Lab Tests, Genetic Testing)
Surgical Devices (e.g., Robotic Surgery Systems, Surgical Implants)
Monitoring Devices (e.g., Cardiac Monitors, CGMs, Remote Monitoring)
Wearable Devices (e.g., Smart Watches, Sleep Monitors)
Software as a Medical Device (SaMD) (e.g., Mobile Health Apps, AI Diagnostics)
Consumer Health and Wellness Product Studies (e.g., Supplements, Cosmetics, OTC Products)
CRA Systems Familiarity
*
Oracle InForm
Medidata Rave
Veeva Vault EDC
OpenClinica
Medrio EDC
IBM Clinical Development
TrialStat EDC
Castor EDC
Veeva Vault eTMF
Trial Interactive eTMF
Wingspan eTMF
Florence eBinders
SiteVault (Veeva)
Oracle Siebel CTMS
Medidata CTMS
Veeva Vault CTMS
Trial Interactive CTMS
Clinical Conductor CTMS
GoBalto Activate
Veeva Vault Study Startup
Cognizant Shared Investigator Platform (SIP)
Clario (eCOA/ePRO/IRT/Imaging)
Other
CTM/CPM Systems Familiarity
*
Veeva Vault CTMS
Medidata CTMS
Oracle Siebel CTMS
Trial Interactive CTMS
Clinical Conductor CTMS
Oracle InForm
Medidata Rave
OpenClinica
Medrio EDC
GoBalto Activate
Veeva Vault Study Startup
Trial Interactive Study Startup
Cognizant Shared Investigator Platform (SIP)
Greenphire
DrugDev Spark
Veeva Vault Investigator Portal
Veeva Vault eTMF
Trial Interactive eTMF
Wingspan eTMF
Clario (eCOA/ePRO/IRT/Imaging)
Other
TMF Management Systems Familiarity
*
Veeva Vault eTMF
Trial Interactive eTMF
Wingspan eTMF
OpenText eTMF
PhlexEview (Phlexglobal)
Florence eBinders
SiteVault (Veeva)
MasterControl Documents
SharePoint-Based eTMF (custom builds)
Other
Clinical Data Manager Systems Familiarity
*
Medidata Rave
Oracle InForm
Veeva Vault EDC
OpenClinica
Medrio EDC
IBM Clinical Development
TrialStat EDC
Castor EDC
Clario (eCOA/ePRO/IRT/Imaging)
Medidata Coder
SAE Reconciliation Platforms
Clinical Data Repositories (CDR)
Other
Biostatistician / SAS Programmer Systems Familiarity
*
SAS
R
JMP Clinical
East Software (Cytel)
nQuery
PASS
WinNonlin (Phoenix)
Medidata Rave (for data extraction)
Oracle InForm (for data extraction)
Spotfire
Clario Imaging Systems
Other
Pharmacovigilance / Drug Safety Systems Familiarity
*
Oracle Argus Safety
ArisGlobal LifeSphere
Veeva Vault Safety
MedDRA Browser / MedDRA Coding Tools
WHO Drug Dictionaries (WHODrug)
Empirica Signal
PV-Works
SAE Reconciliation Platforms
Other
Regulatory Systems Familiarity
*
Veeva Vault RIM (Regulatory Information Management)
MasterControl Regulatory Suite
EXTEDO eCTDmanager
Lorenz docuBridge
GlobalSubmit (now part of Certara Synchrogenix)
Wingspan Regulatory Solutions (Veeva Partnered)
DIA Electronic Document Management Systems (EDMS)
eCTD Submission Tools (generic or proprietary)
Regulatory Information Management Systems (RIMS) (generic)
Health Authority Correspondence Trackers
Other
Patient Recruitment Specialist Systems Familiarity
*
Trialbee
Citeline Connect
StudyKIK
BBK Worldwide
Antidote Match
TrialScope
Clinical Trials GPS
Site Patient Recruitment Platforms (generic)
Other
General Business and Collaboration Systems Familiarity
*
MS Teams
Zoom
Microsoft Outlook
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
SharePoint
Smartsheet
Box
Google Workspace (Docs, Sheets, Drive)
Asana
Jira
Salesforce
Tableau
Power BI
Spotfire
Monday.com
Other
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Your Credentials
Upload your resume, certifications, licenses, and (optionally) a motivation letter to complete your application.
Upload Resume/CV
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Upload your current resume or CV (PDF or Word format preferred, max 5MB)
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Upload Certifications and Licenses
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Optional: Upload any relevant professional certifications (e.g., GCP, CRA, PV) and licenses (e.g., MD, RN, Pharmacist). PDF preferred, maximum size 5MB.
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Upload Motivation Letter
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Optional: Upload a short Motivation Letter (PDF or Word format preferred, maximum 1 page) highlighting your goals, motivations, and alignment with clinical research or drug development roles.
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Review and Submit
Please review your information carefully before submitting your application. By submitting, you confirm that the information provided is accurate and complete to the best of your knowledge.
I confirm that the information I have provided is accurate and complete to the best of my knowledge.
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