Arthrex

Clinical Study Manager (Remote)

Arthrex • $84K — $110K *
US-Anywhere
+ 2 other locationsRemote
Pharmaceuticals & Biotech
Less than 5 years of experience
Today
Be an Early Applicant
Job Overview by Ladders

Qualifications

  • Bachelor's degree required.
  • 4 years of relevant clinical research experience required.
  • Clinical Research Certification required, or must be willing to obtain within 1 year of employment.
  • Preferred familiarity with orthopedic terminology.
  • Preferred experience in industry sponsor or CRO employment.

Responsibilities

  • Plan and execute clinical studies in accordance with research ethics and ISO standards.
  • Lead cross-functional collaboration for project alignment across various departments.
  • Provide timely updates and status reports on clinical research projects.
  • Facilitate compliance documentation for healthcare professional value transfers.
  • Assist with electronic data capture systems and user testing for studies.

Benefits

  • Medical, Dental and Vision Insurance
  • Company-Provided Life Insurance
  • Flexible Spending Account (FSA)
  • Matching 401(k) Retirement Plan
  • Paid Time Off
  • Tuition Reimbursement Program
  • Employee Assistance Provider (EAP)
Full Job Description
Location:Remote Salary Range:Salary Minimum:$84,000.00Salary Maximum: $110,000.00

This is a fully remote opportunity.

Essential Duties and Responsibilities:
  • Planning, executing, managing, and oversight of clinical studies and projects according to Research ethics guidelines, ISO standards, internal SOPs, and portfolio priorities.
  • Serve as a cross-functional lead within an assigned study portfolio, ensuring alignment across Clinical Operations, Product Management, Data Management, Regulatory, Compliance, and other key stakeholders.
  • Provide accurate, timely status reports and portfolio-level updates on assigned clinical research studies and projects.
  • Facilitate appropriate documentation to maintain compliance with the AP and Compliance department for HCP transfers of value.
  • Facilitate clinical contract agreements between Arthrex and the Site for studies.
  • Assist the data management team with electronic data capture systems CRF design, eTMF design, CTMS design and user testing for assigned studies.
  • Provide centralized communication and coordination between research sites and internal cross-functional stakeholders.
  • Facilitate site training for data collection clinical research initiatives.
  • Monitor data collection compliance and communicate with sites to optimize data collection.
  • Provide the main line of communication with research sites.
  • Facilitate IRB approval at the site and sponsor level.
  • Oversee and approve site activation activities for studies, ensuring readiness across all functional areas.
  • Collaborate on reviewing protocols, case report forms, and informed consent for clinical studies.
  • Qualify sites for participation in assigned studies.
  • Complete central, remote, and on-site monitoring visits, reports, and follow-up letters.
  • Identify study- and portfolio-level risks or issues, implement mitigation strategies, and develop CAPA plans as appropriate.
  • Works closely with the other clinical research professionals and cross-functional partners to ensure successful study execution.
  • Conduct regular investigator meetings to ensure protocol compliance and site engagement.
  • Actively participate in research committees, study groups, and cross-functional portfolio governance activities to support continuous improvement and strategic alignment.
  • Engage in and support departmental initiatives and cross-functional team projects, collaborating by driving execution, problem-solving, and achievement of key business outcomes.


Knowledge and Skill Requirements/Specialized Courses and/or Training:
  • Strong strategic thinking with the ability to translate goals into actionable project plans.
  • An understanding of cross-functional clinical study processes is required.
  • Good communication, documentation, and record-keeping skills are required.
  • Ability to identify a research hypothesis and proposed outcomes measures to address the hypothesis is required.
  • Ability to read surgical techniques and have a basic understanding of the medical devices necessary to perform the procedure is required.
  • Experience managing research contracts and protocol development is preferred.
  • Able to communicate effectively with physicians, key opinion leaders, and other healthcare personnel.
  • Experience in post-market, real world evidence, longitudinal or health economics studies is preferred.
  • Ability to generate and develop ideas that drive efficiency and impact organizational goals.
  • Ability to approach challenges with an innovative, solution-oriented mindset.


Education and Experience:
  • Bachelor's degree required.
  • 4 years of relevant clinical research experience required.
  • Familiarity with orthopedic terminology is preferred.
  • One year of industry sponsor or CRO employment preferred.
  • Clinical Research Certification required, or must be willing to obtain within 1 year of employment.


Machine, Tools, and/or Equipment Skills:
  • Experience in Microsoft Office, Clinical trial Electronic Data Capture systems, and electronic trial master file is required.
  • Experience in clinical trial management systems is preferred.


Arthrex Benefits
  • Medical, Dental and Vision Insurance
  • Company-Provided Life Insurance
  • Voluntary Life Insurance
  • Flexible Spending Account (FSA)
  • Supplemental Insurance Plans (Accident, Cancer, Hospital, Critical Illness)
  • Matching 401(k) Retirement Plan
  • Annual Bonus
  • Wellness Incentive Program
  • Gym Reimbursement Program
  • Tuition Reimbursement Program
  • Trip of a Lifetime
  • Paid Parental Leave
  • Paid Time Off
  • Volunteer PTO
  • Employee Assistance Provider (EAP)


Making People Better at Arthrex

Lorem ipsum dolor sit amet consectetur. Cras fringilla elementum odio velit.

Job Details

Date: Jun 25, 2026

Requisition ID: 66649

Salary Range:

Job title: Clinical Study Manager (Remote)

Arthrex

Location:

About Arthrex

Arthrex is a global medical device company and a leader in new product development and medical education in orthopedics. The company's mission is to help surgeons treat their patients better, and the company accomplishes this by providing innovative products and surgical procedures that help surgeons achieve better clinical outcomes. Arthrex has a wide range of products, including devices for sports medicine, foot and ankle, hand and wrist, shoulder and elbow, and orthobiologics. The company also offers medical education programs and resources to help surgeons stay up-to-date with the latest surgical techniques and technologies.
Learn more about Arthrex
Size
14,000 employees
Industry
Healthcare
Net Income
$500 million
Founded
1981
5 Year Trend
+15%
Revenue
$2.3 billion
* Ladders Estimates

Similar Jobs

Ad banner background

Get Ready For Your
Next Interview

More Jobs at Arthrex

More Pharmaceuticals & Biotech Jobs

Find similar Clinical Study Manager (Remote) jobs:

NationwideRemote