5 Study Coordinator Job Description Templates and Examples

Company Overview

[$COMPANY_OVERVIEW]

Role Overview

We are looking for a motivated Junior Study Coordinator to join our research team. In this role, you will assist in the planning and execution of clinical studies, ensuring that all protocols are followed and that our research meets the highest standards of quality. You will have the opportunity to learn from experienced team members and contribute to essential research that drives innovation in our field.

Responsibilities

• Assist in the preparation and organization of study materials, including protocols, consent forms, and case report forms
• Support the recruitment and enrollment of study participants, ensuring compliance with ethical guidelines
• Maintain accurate and detailed records of study-related activities and data
• Coordinate with various stakeholders, including clinical teams, regulatory bodies, and external vendors
• Participate in the monitoring of study progress, identifying issues and assisting in their resolution
• Contribute to the analysis and interpretation of study data, preparing reports as needed

Required Qualifications

• Bachelor's degree in a relevant field (e.g., life sciences, public health, or related discipline)
• Strong attention to detail and organizational skills
• Excellent verbal and written communication abilities
• Ability to work independently and as part of a team in a fast-paced environment
• Familiarity with clinical research principles and practices is a plus, but not required

Preferred Qualifications

• Experience with data management and statistical software (e.g., SPSS, R, or similar tools)
• Previous internship or coursework related to clinical research
• Knowledge of Good Clinical Practice (GCP) guidelines

Benefits and Perks

Salary: [$SALARY_RANGE]

We offer a comprehensive benefits package that may include:

• Health, dental, and vision insurance
• Flexible working hours
• Professional development opportunities
• Annual learning stipend
• Generous paid time off policy

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, gender, national origin, age, disability, or any other protected status.

Location

This is a fully remote position.

Company Overview

[$COMPANY_OVERVIEW]

Role Overview

We are seeking a meticulous and detail-oriented Study Coordinator to join our dedicated research team. In this role, you will be instrumental in the planning, execution, and management of clinical studies, ensuring compliance with regulatory requirements and adherence to study protocols. Your expertise will contribute to advancing our mission of delivering innovative healthcare solutions.

Responsibilities

• Coordinate the operational aspects of clinical studies, including site selection, initiation, and monitoring
• Develop and maintain study documentation, such as protocols, informed consent forms, and case report forms
• Ensure compliance with Good Clinical Practice (GCP) and applicable regulatory guidelines throughout the study lifecycle
• Collaborate with cross-functional teams including investigators, sponsors, and regulatory authorities to ensure successful study execution
• Manage study budgets and timelines, tracking key milestones and deliverables
• Facilitate communication among study stakeholders, providing regular updates on study progress and outcomes
• Oversee data collection, entry, and analysis to ensure data integrity and accuracy

Required Qualifications

• Bachelor’s degree in life sciences, nursing, or a related field
• 2+ years of experience in clinical research, with a strong understanding of clinical trial processes and regulations
• Demonstrated ability to manage multiple projects simultaneously while maintaining attention to detail
• Proficient in electronic data capture systems and clinical trial management software
• Strong analytical and problem-solving skills, with the ability to interpret and present data effectively

Preferred Qualifications

• Certification in Clinical Research (e.g., ACRP or SOCRA) is a plus
• Experience in therapeutic areas relevant to our research focus
• Strong knowledge of statistical analysis and data management principles

Technical Skills and Relevant Technologies

• Familiarity with EHR systems and databases used in clinical research
• Proficient in Microsoft Office Suite (Word, Excel, PowerPoint) and data analysis software
• Experience with remote monitoring tools and electronic trial management systems

Soft Skills and Cultural Fit

• Excellent verbal and written communication skills, with the ability to engage effectively with diverse stakeholders
• Strong organizational and time management skills, demonstrating an ability to prioritize tasks in a fast-paced environment
• A proactive and collaborative approach, with a passion for improving patient outcomes through research
• Commitment to maintaining confidentiality and ethical standards in research

Benefits and Perks

Salary: [$SALARY_RANGE]

Full-time offers include:

• Comprehensive health, dental, and vision insurance
• Generous paid time off and holiday policies
• 401(k) plan with company match
• Professional development opportunities and continuing education support
• Wellness programs and resources to support work-life balance

Equal Opportunity Statement

[$COMPANY_NAME] is committed to fostering a diverse and inclusive workplace. We are proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, sex, gender expression or identity, sexual orientation, or any other basis protected by applicable law.

Location

This is a fully remote position.

We encourage applicants from diverse backgrounds and experiences to apply, even if you do not meet all the qualifications listed.

Company Overview

[$COMPANY_OVERVIEW]

Role Overview

We are seeking a highly motivated and experienced Senior Study Coordinator to join our dynamic team at [$COMPANY_NAME]. In this role, you will play a pivotal role in the planning, execution, and management of clinical studies, ensuring they are conducted in compliance with regulatory requirements and industry standards. You will leverage your expertise to foster collaboration among cross-functional teams while overseeing study timelines, budgets, and deliverables.

Responsibilities

• Lead the planning and execution of clinical studies from protocol development through final study report, ensuring adherence to timelines and budgets.
• Coordinate with internal stakeholders and external vendors to ensure successful study execution, including site selection, training, and management.
• Develop and maintain study-related documentation, including protocols, informed consent forms, and study manuals, ensuring compliance with regulatory guidelines.
• Monitor study progress, identifying and mitigating risks to ensure studies remain on track and within budget.
• Provide regular updates to management and stakeholders on study status, including recruitment metrics, site performance, and budget adherence.
• Mentor and provide guidance to junior study coordinators, fostering a culture of continuous improvement and professional development.

Required and Preferred Qualifications

Required:

• Bachelor's degree in life sciences, healthcare, or a related field.
• 5+ years of experience in clinical research, with a focus on study coordination and management.
• In-depth knowledge of GCP, FDA regulations, and other relevant regulatory guidelines.
• Proven track record of managing multiple studies simultaneously while meeting deadlines and maintaining quality standards.

Preferred:

• Advanced degree (Master's or PhD) in a relevant field.
• Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Strong project management skills with relevant certifications (e.g., PMP, ACP).

Technical Skills and Relevant Technologies

• Proficiency in clinical trial management software and data management systems.
• Strong analytical skills with the ability to interpret complex data and make informed decisions.
• Familiarity with statistical software packages and data analysis.

Soft Skills and Cultural Fit

• Exceptional communication and interpersonal skills, with the ability to build relationships across diverse teams.
• Strong organizational skills with a keen attention to detail.
• Ability to thrive in a fast-paced, dynamic environment while maintaining a positive attitude.
• A collaborative mindset with a focus on fostering teamwork and inclusivity.

Benefits and Perks

Annual salary range: [$SALARY_RANGE]

Additional benefits may include:

• Comprehensive health insurance plans, including dental and vision coverage.
• Flexible work hours and the option for remote work within [$COMPANY_LOCATION].
• Generous paid time off and holidays.
• Retirement savings plans with company matching.
• Professional development opportunities and tuition reimbursement.

Equal Opportunity Statement

[$COMPANY_NAME] is committed to creating a diverse and inclusive workplace. We encourage applications from candidates of all backgrounds and experiences. All qualified applicants will receive consideration for employment without regard to race, color, religion, sexual orientation, gender identity or expression, national origin, age, disability, or veteran status.

Location

This is a remote position within [$COMPANY_LOCATION].

Company Overview

[$COMPANY_OVERVIEW]

Role Overview

We are seeking a skilled and detail-oriented Lead Study Coordinator to oversee and manage clinical study operations within our organization. In this role, you will be responsible for leading the planning, execution, and completion of clinical trials, ensuring adherence to regulatory requirements and study protocols while fostering collaboration among cross-functional teams.

Responsibilities

• Lead the development and implementation of study protocols, ensuring compliance with regulatory requirements and industry standards.
• Coordinate and facilitate communication among investigators, study teams, and stakeholders to ensure timely and accurate execution of clinical trials.
• Oversee site selection, initiation, monitoring, and close-out activities, ensuring adherence to timelines and budgets.
• Manage and mentor study coordinators and staff, fostering a culture of continuous improvement and professional development.
• Develop and maintain study documentation, including study plans, regulatory submissions, and site training materials.
• Analyze and report on study progress, identifying potential risks and implementing corrective actions as necessary.
• Ensure patient safety and data integrity throughout the study lifecycle by adhering to Good Clinical Practice (GCP) guidelines.

Required and Preferred Qualifications

Required:

• Bachelor's degree in a relevant field (e.g., life sciences, nursing, or related discipline).
• 5+ years of experience in clinical research, with a focus on study coordination and management.
• Strong understanding of GCP, FDA regulations, and other applicable guidelines.
• Proven experience in leading clinical trials and managing cross-functional teams.
• Excellent organizational, communication, and interpersonal skills.

Preferred:

• Advanced degree (e.g., Master's, PhD) in a relevant field.
• Experience with electronic data capture (EDC) systems and clinical trial management software (CTMS).
• Certification as a Clinical Research Coordinator (CRC) or Clinical Research Associate (CRA).

Technical Skills and Relevant Technologies

• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and project management tools.
• Experience with clinical trial software and databases.
• Familiarity with data analysis and reporting tools.

Soft Skills and Cultural Fit

• Strong leadership skills with a collaborative mindset.
• Ability to adapt to changing priorities and maintain focus under pressure.
• Strong problem-solving skills and attention to detail.
• Commitment to ethical standards and a patient-centric approach.
• A proactive and enthusiastic attitude towards learning and professional growth.

Benefits and Perks

Salary range: [$SALARY_RANGE]

Full-time positions may include:

• Comprehensive health insurance plans, including medical, dental, and vision coverage.
• Generous paid time off and flexible work arrangements.
• Retirement savings plans with company matching contributions.
• Professional development opportunities and support for continuing education.
• Wellness programs and resources to support mental health and work-life balance.

Equal Opportunity Statement

[$COMPANY_NAME] is dedicated to fostering an inclusive work environment and is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other characteristic protected by applicable law. We encourage applicants from diverse backgrounds to apply.

Location

This is a remote position within [$COMPANY_LOCATION]. We welcome candidates from diverse geographic regions within the specified location.

Company Overview

[$COMPANY_OVERVIEW]

Role Overview

We are seeking a highly organized and detail-oriented Clinical Research Coordinator to manage and oversee clinical trials from initiation to completion. This fully remote role is essential in ensuring that our research adheres to regulatory requirements and meets the highest standards of quality, contributing to advancements in medical science.

Responsibilities

• Coordinate all aspects of clinical trial activities, including participant recruitment, screening, and enrollment
• Maintain compliance with study protocols, regulatory requirements, and institutional policies
• Regularly communicate with investigators, study sponsors, and regulatory bodies to ensure trial progress and adherence
• Manage and document all trial-related data accurately and in a timely manner, including case report forms and participant records
• Prepare and submit regulatory documents and reports as required
• Monitor trial progress and participant safety, addressing any issues proactively
• Conduct training sessions for site staff on study protocols and procedures
• Assist in the analysis and interpretation of clinical data, contributing to study reports and publications

Required and Preferred Qualifications

Required:

• Bachelor's degree in a life science or related field
• 2+ years of experience in clinical research coordination or management
• Strong understanding of Good Clinical Practice (GCP) and regulatory requirements
• Excellent organizational skills, attention to detail, and ability to manage multiple tasks simultaneously
• Proficient in using clinical trial management systems and electronic data capture tools
• Strong written and verbal communication skills

Preferred:

• Certification as a Clinical Research Coordinator (CRC) or Clinical Research Associate (CRA)
• Experience with patient recruitment strategies and community engagement
• Knowledge of statistical analysis and data interpretation

Technical Skills and Relevant Technologies

• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and clinical trial software
• Experience with electronic health records (EHR) systems
• Familiarity with statistical software (e.g., SAS, SPSS) is a plus

Soft Skills and Cultural Fit

• Demonstrated ability to work independently and as part of a remote team
• Strong problem-solving skills and the ability to adapt to changing situations
• Passion for advancing medical research and improving patient outcomes
• Commitment to maintaining confidentiality and ethical standards in research

Benefits and Perks

Salary: [$SALARY_RANGE]

Full-time employees are eligible for:

• Comprehensive health, dental, and vision insurance
• 401(k) retirement plan with company matching
• Generous paid time off and holidays
• Opportunities for professional development and continuing education
• Flexible work hours and a supportive remote work environment

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, creed, gender, national origin, age, disability, veteran status, sex, gender expression or identity, sexual orientation, or any other basis protected by applicable law.

Location

This is a fully remote position.