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  3. Clinical Research Coordinator I (On-site/ Raleigh)
M3

Clinical Research Coordinator I (On-site/ Raleigh)

M3USA·Raleigh, North Carolina

Full Time·On Site·2-5 yrs·Posted 2 months ago
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About the role

The Clinical Research Coordinator manages daily clinical trial activities and supports the Principal Investigator in the conduct of studies. Key duties include screening participants, maintaining documentation, and ensuring compliance with research protocols and laws.

Company DescriptionM3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs).

With close to 30 owned and managed research sites across the country, M3 Wake Research is one of the largest independent, multi-site clinical research companies in the US.

M3 Wake Research continues to grow through acquisitions and uncompromising commitment to careful planning and execution in accordance with regulatory compliance.Conducting studies since 1984, M3 Wake Research owns a proprietary patient database of potential clinical trial participants across the US.

As of today, our board-certified physicians have completed more than 7,000+ successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data.Due to our continued growth, we are hiring for a Clinical Research Coordinator at Wake Research, an M3 company.

This position is on-site and located in Raleigh, NC.

Job DescriptionThe Clinical Research Coordinator (CRC) is a specialized research professional working with and under the guidance of the clinical research site management and Principal Investigator (PI).

While the PI is primarily responsible for the overall conduct of the clinical trial, the CRC manages, supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.

Essential

Duties and Responsibilities

Assisting trial Investigator in screening and review of potential study participants eligibilityMaintaining case report forms, charts and documentationMentoring, training, and high-level oversight of other clinical research coordinators and research assistantsEnsuring that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirementsCollecting and entering data as necessaryAssist management with potential new hire selection and shadowing processAssist with study start-up, maintenance, and close-out of studies as needed for those on the teamAbility to be flexible with study assignmentsQualificationsClinical Research Coordinator with 1-2 years of experiencePhlebotomy experience is highly preferredExcellent verbal & written communication skillsAbility to learn quickly, read and understand complex protocols, follow very detailed directions, and multi-taskingMust be able to maintain strict confidentiality of patients, employees, and company information at all times and adhere to HIPAA GuidelinesExtensive clinical trial knowledge through education and/or experienceSuccessful completion of GCP Certification and Advanced CRC preferredDetail-orientedFamiliarity with the Code of Federal Regulations as they pertain to human subject protectionStrong interpersonal skillsAdditional InformationAbout M3: M3 USA is at the forefront of healthcare innovation, offering digital solutions across healthcare, life sciences, pharmaceuticals, and more. Since our inception in 2000, we’ve seen remarkable growth, fueled by our mission to utilize the internet for a healthier world and more efficient healthcare systems.Our success is anchored in our trusted digital platforms that engage physician communities globally, facilitating impactful medical education, precise job placement, and insightful market research. M3 USA prides itself on a dynamic and innovative work environment where every team member contributes to global health advancements.Joining M3 USA means being part of a dedicated team striving to make a significant difference in healthcare. We provide a unique opportunity for you to be at the cutting edge of healthcare innovation, shaping the future in a meaningful career. Embrace the chance to drive change with M3 USA.Benefits: A career opportunity with M3 Wake Research offers competitive wages, and benefits such as:401(k), 401(k) matchingDental insuranceDisability insuranceEmployee assistance programFlexible spending accountHealth insuranceLife insurancePaid time offVision insurance*M3 reserves the right to change this job description to meet the business needs of the organization#LI-Onsite#LI-LB1

Requirements

Candidates must have at least 2 years of experience as a Clinical Research Coordinator and extensive knowledge of clinical trials. Phlebotomy experience and GCP Certification are highly preferred.

  • professional certificate
  • Interpersonal Skills
  • Written Communication
  • Verbal Communication
  • Multi-tasking
  • HIPAA Compliance
  • Regulatory Compliance
  • Phlebotomy
  • Data Entry
  • Patient Screening
  • Clinical Trial Management
  • Case Report Forms
  • GCP Certification

Benefits

  • Dental Insurance
  • Disability Insurance
  • Employee Assistance Program
  • Life Insurance
  • Paid Time Off
  • Health Insurance
  • Vision Insurance
  • 401(k)
  • Flexible Spending Account
  • 401(k) Matching

Posting details

Employment type
Full Time
Work arrangement
On Site
Experience
2-5 yrs
Location
Raleigh, North Carolina
Posted
May 8, 2026
Application
Employer website
M3

Hiring organization

M3USA

M3 Wake Research is a premier clinical trial network that has been conducting studies since 1984. With over 30 years of experience, the network's subject database for clinical trial participants has substantial potential and continues to expand as we grow our network across the...

IndustryBiotechnology Research
TypePrivately Held
Size201-500 employees
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