5 Clinical Research Coordinator Job Description Templates and Examples

Company Overview

[$COMPANY_OVERVIEW]

Role Overview

We are looking for a motivated Junior Clinical Research Coordinator to join our clinical research team at [$COMPANY_NAME]. In this entry-level role, you will support the planning, execution, and management of clinical trials while ensuring compliance with regulatory standards and ethical guidelines. This position is ideal for individuals passionate about advancing healthcare through research and gaining valuable hands-on experience in a clinical environment.

Responsibilities

• Assist in the preparation and maintenance of study-related documents, including protocols, informed consent forms, and case report forms.
• Coordinate study activities, including participant recruitment, enrollment, and follow-up.
• Ensure adherence to study protocols and regulatory requirements by conducting site visits and audits.
• Support data collection, management, and analysis, ensuring accuracy and completeness of clinical trial data.
• Communicate effectively with study participants, investigators, and interdisciplinary teams to facilitate smooth study operations.
• Participate in training sessions and workshops to enhance knowledge of clinical research practices and methodologies.

Required and Preferred Qualifications

Required:

• Bachelor's degree in a relevant field such as life sciences, health sciences, or a related discipline.
• Strong organizational skills and attention to detail.
• Excellent verbal and written communication skills.

Preferred:

• Previous experience in a clinical research setting, internships, or relevant coursework.
• Familiarity with Good Clinical Practice (GCP) guidelines and regulatory requirements.

Technical Skills and Relevant Technologies

• Basic understanding of clinical trial phases and processes.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
• Familiarity with electronic data capture systems is a plus.

Soft Skills and Cultural Fit

• Strong interpersonal skills and the ability to work collaboratively in a team environment.
• A proactive attitude with a willingness to learn and adapt in a fast-paced research setting.
• Commitment to maintaining confidentiality and ethical standards in research.

Benefits and Perks

We offer a competitive salary and comprehensive benefits package, including:

• Health, dental, and vision insurance.
• Retirement savings plan with company matching.
• Paid time off and holidays.
• Opportunities for professional development and continuing education.

Location

This role requires successful candidates to be based in-person at our facility located in [$COMPANY_LOCATION].

Company Overview

[$COMPANY_OVERVIEW]

Role Overview

We are looking for a detail-oriented Clinical Research Coordinator to join our innovative research team at [$COMPANY_NAME]. In this role, you will play a critical part in managing clinical trials and ensuring compliance with regulatory standards. You will act as a liaison between study participants, investigators, and regulatory agencies, driving the success of clinical studies that advance medical research and patient care.

Responsibilities

• Oversee the coordination and administration of clinical trials, ensuring adherence to protocols and regulatory requirements.
• Recruit, screen, and enroll study participants while maintaining their safety and confidentiality.
• Collect, manage, and analyze clinical data, ensuring accuracy and completeness in accordance with Good Clinical Practice (GCP).
• Facilitate communication between investigators, study sponsors, and regulatory bodies, fostering collaborative relationships.
• Develop and maintain study documentation, including informed consent forms, case report forms (CRFs), and study binders.
• Monitor trial progress and troubleshoot any issues that arise, implementing corrective actions as necessary.

Required and Preferred Qualifications

Required:

• Bachelor's degree in a related field (e.g., life sciences, nursing, public health).
• 2+ years of experience in clinical research coordination or a similar role.
• Strong understanding of clinical trial regulations, protocols, and research methodologies.
• Excellent organizational and time-management skills with a keen attention to detail.
• Strong interpersonal and communication skills to effectively engage with diverse stakeholders.

Preferred:

• Certification from a recognized clinical research organization (e.g., ACRP, SOCRA).
• Experience with electronic data capture (EDC) systems and clinical trial management software.
• Knowledge of statistical analysis and data interpretation.

Technical Skills and Relevant Technologies

• Proficiency in Microsoft Office Suite, particularly Excel for data management and analysis.
• Familiarity with clinical trial management systems (CTMS) and electronic health records (EHR).
• Experience with data analysis software or statistical packages such as SPSS or SAS.

Soft Skills and Cultural Fit

• Demonstrated ability to work independently and collaboratively within a team.
• Proactive problem-solving skills with a focus on continuous improvement.
• Adaptability to changing priorities in a fast-paced environment.
• Commitment to ethical standards and patient welfare.

Benefits and Perks

Salary range: [$SALARY_RANGE]

Our comprehensive benefits package may include:

• Health, dental, and vision insurance
• Retirement savings plan with employer matching
• Generous paid time off and holiday schedule
• Professional development opportunities and support for continuing education
• Wellness programs and employee assistance services

Equal Opportunity Statement

[$COMPANY_NAME] is committed to fostering a diverse workplace and is proud to be an Equal Opportunity Employer. We encourage applicants from all backgrounds and walks of life to apply, and we will consider all qualified candidates without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other characteristic protected by law.

Location

This role requires successful candidates to be based in-person at our facility located in [$COMPANY_LOCATION].

We encourage applicants to apply even if they don’t meet every requirement outlined in this description. Your unique experiences and perspectives can contribute significantly to our team!

Company Overview

[$COMPANY_OVERVIEW]

Role Overview

We are seeking a highly skilled and motivated Senior Clinical Research Coordinator to join our clinical operations team. In this role, you will play a critical part in managing clinical trials, ensuring compliance with regulatory standards, and fostering collaboration among cross-functional teams. Your expertise will be pivotal in driving the successful execution of clinical studies that contribute to innovative research and patient care.

Responsibilities

• Lead and coordinate all aspects of clinical trial management, including site selection, initiation, monitoring, and closeout activities
• Develop and maintain study-related documentation, including protocols, informed consent forms, and case report forms, ensuring adherence to Good Clinical Practice (GCP)
• Oversee the recruitment and retention of study participants, establishing strong relationships with sites and stakeholders
• Collaborate with regulatory affairs to ensure timely submission of documents and compliance with all regulatory requirements
• Monitor trial progress, analyze data trends, and provide regular updates to stakeholders, including study sponsors and investigators
• Mentor and train junior coordinators and staff on best practices in clinical research and trial management

Required and Preferred Qualifications

Required:

• 5+ years of experience in clinical research coordination or related field, with a strong understanding of clinical trial processes
• Proven expertise in regulatory compliance, GCP guidelines, and ethical considerations in clinical research
• Excellent organizational skills and attention to detail, with the ability to manage multiple priorities effectively

Preferred:

• Advanced degree in life sciences, nursing, or related field
• Experience with electronic data capture (EDC) systems and clinical trial management software
• Certification from a recognized clinical research organization (e.g., ACRP or SoCRA)

Technical Skills and Relevant Technologies

• Proficient in using EDC systems, data management software, and Microsoft Office Suite
• Familiarity with biostatistical software and data analysis tools
• Strong understanding of medical terminology and clinical trial protocols

Soft Skills and Cultural Fit

• Exceptional communication and interpersonal skills, with the ability to liaise effectively with diverse teams
• Strong problem-solving abilities and a proactive approach to addressing challenges
• A passion for clinical research and commitment to improving patient outcomes
• Ability to thrive in a fast-paced, dynamic environment while maintaining a positive attitude

Benefits and Perks

Annual salary range: [$SALARY_RANGE]

In addition to a competitive salary, we offer a comprehensive benefits package that may include:

• Health, dental, and vision insurance
• Retirement savings plans with employer matching
• Generous paid time off and flexible work arrangements
• Professional development opportunities and support for continuing education

Equal Opportunity Statement

[$COMPANY_NAME] is committed to creating a diverse environment and is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Location

This is a remote position within [$COMPANY_LOCATION]. We encourage applicants from diverse backgrounds and experiences to apply, even if they do not meet all the listed qualifications.

Company Overview

[$COMPANY_OVERVIEW]

Role Overview

We are looking for a highly skilled and experienced Lead Clinical Research Coordinator to oversee the execution of clinical trials and ensure compliance with regulatory requirements. In this pivotal role, you will coordinate the operational aspects of clinical studies, working closely with cross-functional teams to drive research excellence and improve patient outcomes.

Responsibilities

• Lead the planning, execution, and oversight of clinical trials, ensuring adherence to protocols, timelines, and budgets
• Develop and implement study protocols, informed consent documents, and monitoring plans
• Collaborate with investigators, sponsors, and regulatory bodies to facilitate successful study execution
• Ensure compliance with FDA regulations, ICH/GCP guidelines, and institutional policies
• Manage site selection, training, and performance evaluation of study personnel
• Track and report study progress, including patient recruitment, data collection, and regulatory submissions
• Provide mentorship and training to junior coordinators and staff, fostering a culture of continuous improvement

Required and Preferred Qualifications

Required:

• Bachelor's degree in life sciences or a related field
• 5+ years of clinical research experience, including 2+ years in a lead or supervisory role
• Strong understanding of clinical trial design, methodology, and regulatory requirements
• Proven ability to manage multiple projects and meet deadlines in a fast-paced environment

Preferred:

• Advanced degree (Master's or Doctorate) in a relevant field
• Experience in therapeutic areas relevant to ongoing research at [$COMPANY_NAME]
• Certification from ACRP or SOCRA

Technical Skills and Relevant Technologies

• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems
• Familiarity with statistical analysis software and data management tools
• Strong analytical skills for interpreting clinical data and reports

Soft Skills and Cultural Fit

• Exceptional communication skills, both verbal and written, with the ability to convey complex information clearly
• Strong organizational and problem-solving skills, with attention to detail
• Ability to work collaboratively within a multidisciplinary team and build effective relationships
• Proactive mindset with a focus on continuous learning and professional development

Benefits and Perks

Annual salary range: [$SALARY_RANGE]

Additional benefits may include:

• Health, dental, and vision insurance
• 401(k) retirement plan with company match
• Generous paid time off (PTO) and holiday schedule
• Professional development opportunities and tuition reimbursement
• Flexible working hours and remote work options

Equal Opportunity Statement

[$COMPANY_NAME] is committed to diversity and inclusion in the workplace and is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, age, disability, veteran status, or any other characteristic protected by applicable law.

Location

This is a remote position within [$COMPANY_LOCATION].

We encourage applicants from diverse backgrounds and experiences to apply, even if you don't meet all the qualifications listed. Your unique perspectives and skills can contribute to our mission of excellence in clinical research.

Company Overview

[$COMPANY_OVERVIEW]

Role Overview

We are seeking a highly skilled and motivated Clinical Research Manager to oversee and drive the execution of clinical trials within our innovative research team. This role is integral to ensuring the successful planning, implementation, and completion of clinical studies that meet regulatory requirements and align with our strategic goals. You will collaborate with cross-functional teams to enhance patient outcomes and support the advancement of our groundbreaking therapies.

Responsibilities

• Lead the planning, execution, and management of clinical trials, ensuring adherence to timelines, budgets, and compliance with regulatory standards
• Develop and implement study protocols, informed consent forms, and other essential clinical documentation
• Oversee data collection and ensure the integrity and accuracy of clinical data
• Manage relationships with key stakeholders, including clinical sites, vendors, and regulatory authorities
• Provide mentorship and guidance to clinical research staff, fostering a culture of excellence and continuous improvement
• Conduct site selection, initiation, monitoring, and closure activities, ensuring high-quality study execution
• Prepare and present study updates and findings to senior management and external stakeholders

Required and Preferred Qualifications

Required:

• Bachelor's degree in Life Sciences, Nursing, or a related field
• 5+ years of experience in clinical research, with a strong understanding of GCP, ICH guidelines, and relevant regulatory requirements
• Proven track record of managing clinical trials from initiation through completion
• Exceptional organizational skills and attention to detail
• Strong analytical and problem-solving abilities

Preferred:

• Advanced degree (Master's or Doctorate) in a relevant field
• Experience in therapeutic areas relevant to our research focus
• Proficiency in electronic data capture (EDC) systems and clinical trial management software
• Demonstrated success in leading cross-functional teams in a fast-paced environment

Technical Skills and Relevant Technologies

• Deep understanding of clinical trial methodologies and processes
• Experience with statistical analysis software and data management tools
• Familiarity with patient recruitment strategies and retention techniques

Soft Skills and Cultural Fit

• Outstanding written and verbal communication skills
• Ability to build strong relationships with a diverse group of stakeholders
• Proactive, adaptable, and results-oriented mindset
• Commitment to ethical conduct and integrity in research practices
• Passion for advancing healthcare and improving patient outcomes

Benefits and Perks

Salary range: [$SALARY_RANGE]

Full-time employees can enjoy a robust benefits package that may include:

• Comprehensive health insurance (medical, dental, and vision)
• 401(k) plan with company matching
• Generous paid time off and holidays
• Flexible work arrangements and remote work options
• Professional development opportunities and tuition reimbursement

Equal Opportunity Statement

[$COMPANY_NAME] is committed to fostering a diverse and inclusive workplace. We are proud to be an Equal Opportunity Employer and encourage applicants from all backgrounds to apply. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, age, national origin, or disability status.

Location

This is a remote position within [$COMPANY_LOCATION].

We encourage applicants who may not meet every qualification listed to apply, as we value diverse experiences and perspectives.