ZipRecruiter

Log In

2

Remote Clinical Study Start Up Jobs in Raleigh, NC

Adecco

Clinical Trials Manager- Remote

Chapel Hill, NC · Remote

$62 - $64.73/hr

Clinical Trials Manager (CTM) Location: Remote Schedule: Full-Time | Eastern Time Zone Hours Pay ... Coordinate study start-up activities and support timely ethics committee and regulatory submissions.

Ergomed

Senior Site Contracts Specialist

Raleigh, NC · Remote

$95K/yr

Ergomed is a specialist clinical research organization focused on rare disease and select oncology ... Tracks in a timely manner progress of Site contracting activities during Study Start Up or

Ergomed

Senior Site Contracts Specialist

Raleigh, NC · On-site +1

$95K/yr

Ergomed is a specialist clinical research organization focused on rare disease and select oncology ... Tracks in a timely manner progress of Site contracting activities during Study Start Up or

Ergomed

Senior Site Contracts Specialist

Raleigh, NC · Remote

$95K/yr

Ergomed is a specialist clinical research organization focused on rare disease and select oncology ... Tracks in a timely manner progress of Site contracting activities during Study Start Up or

Danaher

Principal Clinical Scientist

Raleigh, NC · On-site +1

... clinical studies in these vital markets. This position is part of the Danaher Diagnostics, Beckman Coulter Inc. organization and will be remote based (can also be onsite in Chaska, MN). At Danaher ...

next page

Showing results 1-20

All JobsClinical Study Start Up JobsRemote Clinical Study Start Up JobsRemote Clinical Study Start Up Jobs in Raleigh, NC

Remote Clinical Study Start Up information

See Raleigh, NC salary details

$21.4K

$121.8K

$200.2K

How much do remote clinical study start up jobs pay per year?

As of Sep 8, 2026, the average yearly pay for remote clinical study start up in Raleigh, NC is $121,792.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,600.00 and $152,600.00 per year, depending on experience, location, and employer.

What is the difference between Remote Clinical Study Start Up vs Remote Clinical Data Coordinator?

AspectRemote Clinical Study Start UpRemote Clinical Data Coordinator
Primary ResponsibilitiesPlanning, site selection, regulatory submissions, site initiationData entry, data validation, database management, data quality assurance
Required CredentialsLife sciences degree, knowledge of GCP, regulatory knowledgeLife sciences or related degree, familiarity with clinical data systems
Work EnvironmentCollaborates with sponsors, sites, regulatory bodiesWorks mainly with data management teams and databases
Industry UsageInvolved early in trial setup phasesInvolved during data collection and analysis phases

Remote Clinical Study Start Up focuses on preparing and initiating clinical trials, including site selection and regulatory compliance. In contrast, Remote Clinical Data Coordinator manages and ensures the accuracy of clinical trial data during the study. Both roles require related credentials and work within the clinical research industry, but they operate at different stages of the trial process.

What are the most commonly searched types of Clinical Study Start Up jobs in Raleigh, NC?

The most popular types of Clinical Study Start Up jobs in Raleigh, NC are:

What are popular job titles related to Remote Clinical Study Start Up jobs in Raleigh, NC?

For Remote Clinical Study Start Up jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Remote Clinical Study Start Up jobs in Raleigh, NC look for?

The top searched job categories for Remote Clinical Study Start Up jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Remote Clinical Study Start Up jobs?

Cities near Raleigh, NC with the most Remote Clinical Study Start Up job openings:

Remote Clinical Study Start Up jobs near you

Clinical Operations Manager

Chapel Hill, NC • On-site, Remote

SiteBridge Research, Inc.
See more jobs at SiteBridge Research, Inc.external

$80K - $95K/yr

Full-time

Posted 14 days ago

Job description

SiteBridge Research Inc:
Founded in 2021, SiteBridge Research is an integrated research organization, focused on building a national network of small and community medical practices to deliver world-class industry sponsored clinical research studies on time and on budget, accelerating time to completing clinical trials, accelerating time to market and product adoption in communities that are often underrepresented and difficult to reach. SiteBridge Research extends reach further into these communities to empower patients with some of the highest unmet needs to take part in clinical studies to improve inclusivity in clinical research and to improve overall health outcomes.
Job Description: The Clinical Operations Manager is an experienced clinical research professional who provides oversight and support to Clinical Research Coordinators (CRCs) and site staff across multiple sites or satellite locations within our site network. This role requires in-depth industry understanding, knowledge, experience, and flexibility to make informed and effective decisions independently. The Operations Manager is responsible for site oversight, including study readiness, CRC and site performance, and overall site performance against key performance metrics for each assigned study. The Operations Manager maintains a staffing plan for the resourcing and utilization of site operations team members across multiple locations or larger sites to achieve performance objectives, identify opportunities or gaps, and implement plans accordingly. This role also supports study start-up, maintenance, and close-out activities, and partners cross-functionally with recruitment, budget, and finance teams to drive site success. In addition, and most importantly, this role represents the SiteBridge Research mission and vision by focusing on the trusted physician/patient partnership from start to finish for every clinical trial conducted at the site and is key in transforming clinical research for every participant. The position will maintain the operational excellence required of clinical sites/staff involved in clinical studies and ensure ICH/GCP and SOP compliance. The person in this role will report to the Executive Director of Site Operations. The position is remote with up to 30% travel at time during peak study activities for candidates with prerequisite experience.
Responsibilities
  • Provide day-to-day oversight of CRCs and site staff across multiple sites or satellite locations, ensuring study readiness, protocol compliance, and consistent execution across the portfolio
  • Own site and CRC performance against key performance metrics for each assigned study, identifying gaps early and implementing corrective action plans
  • Drive accountability for patient enrollment, ensuring sites own the enrollment plan to meet recruitment goals for their specific studies
  • Responsible for CRC hiring, onboarding, training, performance management, and retention across all assigned sites and satellite locations
  • Support project start-up, maintenance, and close-out activities across assigned sites, including study start-up and close-out, recruitment, and regulatory submissions
  • Identify barriers to timely study activation, efficient coordination, and site performance, and partner with appropriate teams to identify and implement solutions
  • Partner cross-functionally with recruitment, budget, and finance teams to drive site success and support forecasting and financial performance at the site level
  • As necessary, step in and fill site and study level needs including but not limited to site set-up and CRC duties to meet SiteBridge and sponsor needs
  • Evaluate and communicate metrics of all activity related to assigned sites and studies, and provide summary findings and recommendations to leadership
  • Track study activities to ensure compliance with standard operating procedures (SOPs), protocols, and all related local, state, and national regulatory and institutional policies
  • Prepare, participate in, and follow-up on audits/inspections as needed, including direction for audit prep and any required follow up post audit
  • Participates in required training and education programs
  • Participate in meetings (ie., Investigator Meetings, Site Trainings, Conferences) and seminars to update knowledge of clinical research and related issues as necessary
  • Other duties and support as assigned related to site and study operations
  • Travel is required (up to 30%) for projects related to site development and operations

Qualifications/Required Experience
  • Bachelor's degree minimum: a combination of education and related technical/professional experience may be substituted for the degree requirements and will be considered on a case-by-case basis
  • Minimum of four (4) years of clinical research or related experience. Experience as a CRC, CRA, Site Lead, Site Manager, or related is required
  • Minimum of 2 years of experience supervising or overseeing CRCs or site staff, including staffing and resource planning, is required
  • Bilingual, Spanish speaking candidates are encouraged to apply
  • Proven success overseeing performance across multiple sites or locations within an organization
  • Demonstrated knowledge of clinical trial operations and execution related to but not limited to start-up, regulatory submission, site feasibility, ect.
  • Excellent working knowledge of FDA & ICH GCP regulations and guidelines is required
  • Experience with eSource, eRegulatory, and CTMS is required
  • Experience in study document preparation (CRF, eSource, logs, SOPs, etc.) is a plus
  • Strong preference for experience within multiple phase research and therapeutic areas
  • Experience with necessary clinical study and staff records related to clinical study activity which includes case report forms, drug dispensation records, etc.
  • Excellent communication skills, attention to detail, problem-solving, follow-through, and organizational skills, with the ability to multi-task and work under/meet deadlines
  • Detail-oriented and meticulous in all aspects of work
  • Superior interpersonal, organization, and management skills
  • Capable of working independently with minimal supervision
  • Understanding of medical terminology as well as standard clinical procedures and protocols

Additional Qualifications
  • Strong project and time management skills
  • High level of collaboration, customer orientation awareness and focus
  • Skilled with standard computer programs including the MS Office suite
  • Strong interpersonal, written, and verbal communication skills

Additional Information
SiteBridge Research, Inc. is proud to be an Equal Opportunity Employer providing employees with a work environment free of discrimination and harassment. We respect and seek to empower each individual and value the diverse cultures, perspectives, skills and experiences within our workforce. We celebrate diversity and do not discriminate based on race, religion, color, national origin, sex, sexual orientation, age, veteran status, disability status, or any other applicable characteristics protected by law. All employment decisions at SiteBridge are based on business needs, job requirements and individual qualifications and performance.
JOB CODE: 26-0014

Apply