Pharmacy Coordinator

Headlands Research

Job Location:

Myrtle Beach, SC - USA

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

At Headlands Research we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018 our rapidly growing company currently operates 20 sites across the US and Canada with plans for further expansion.

Location: Myrtle Beach SC Site Name: Trial Management Associates Full-Time Clinical Research

Are you an experienced medical assistant or pharmacy tech looking to gain a new set of skills Join a leading integrated clinical research network dedicated to high-quality data patient-centered care and innovation in clinical trials.

Were seeking a Pharmacy Coordinator for our clinical research site located in Myrtle Beach SC. The Pharmacy Coordinator plays a key role in the successful execution of pharmaceutical clinical trials by ensuring the safe accurate and compliant handling of the investigational products (IP)/drug that is being studied. Working under the supervision of a licensed pharmacist or nurse (as applicable) this individual will be responsible for receiving storing preparing dispensing documenting and managing investigational drugs in accordance with study protocols GCP/ICH regulations and institutional SOPs. This role may also support administrative and data entry activities related to the conduct of clinical research.

Type: Regular Full-time Employee
Schedule: Mondays through Thursdays 7:00 AM to 4:30 PM and Fridays 7:30 AM to 11:30 AM
Location: Onsite in Myrtle Beach SC (no capabilities for remote or hybrid work)
Reports to: Site Director
Benefits: Our benefits package for full-time employees includes health insurance (medical dental and vision) Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA) Paid Time Off (PTO) a variety of disability accident and life insurance options as well as many more.

What We Offer

Competitive pay annual performance incentives
Medical dental and vision insurance
401(k) plan with company match
Paid time off (PTO) and company holidays
A mission-driven culture focused on advancing medicine and improving patient outcomes

Why Join Us

Youll be part of a growing mission-driven organization that values its people. At our core were committed to bringing innovative medical treatments to patients fasterwhile creating an environment where employees thrive. If youre passionate about clinical research and ready to make a difference wed love to hear from you.

Core Responsibilities:

Investigational Product (IP) Management
- Receive store prepare and dispense investigational products according to protocol pharmacy manual and regulatory requirements.
- Use IWRS/IRT systems to log shipments assign IP and perform returns or destructions per study-specific guidance.
- Maintain accurate inventory logs temperature records and expiration tracking for all IP and supplies.
- Monitor and respond to temperature excursions discrepancies or deviations per SOP.
- Perform aseptic preparations where required following sterile technique protocols.
- Manage IP accountability documentation including blinded and unblinded logs and reconciliation.
- Ensure all investigational product storage complies with GCP and institutional policies (double-locked secure labeled etc.).
Documentation & Compliance
- Maintain audit-ready records of all pharmacy activities including temperature logs equipment calibrations and IP logs.
- Create and manage pharmacy study binders with updated regulatory and protocol-specific content.
- Adhere to ALCOA-C principles (Attributable Legible Contemporaneous Original Accurate Complete and Consistent) in documentation practices.
- Participate in unblinded or blinded monitoring visits providing relevant pharmacy documentation.
Administrative & Operational Support
- Assist with scheduling and performing protocol-specific assessments (e.g. memory assessments vital signs specimen collection support).
- Perform data entry in eCRFs according to protocol and system-specific guidelines.
- Support query resolution documentation scanning and other clerical duties (e.g. faxing reminder calls).
- Order pharmacy-related supplies and assist with equipment upkeep and calibrations.
- Provide pharmacy support to other team members and backfill duties during absences.
Communication & Collaboration
- Maintain clear professional communication with study coordinators monitors sponsors and clinical staff.
- Participate in team meetings and training sessions to stay updated on protocols SOPs and compliance standards.
- Demonstrate flexibility and professionalism in a fast-paced regulated environment.

Requirements:

Minimum of 12 years of experience as a Pharmacy Technician or Medical Assistant required
Completion of a recognized Pharmacy Technician or Medical Assistant program
Registration with relevant state or provincial licensing body (e.g. College of Pharmacists of BC for Pharm Techs for example) required where applicable.
Current certification in Good Clinical Practice (GCP) and/or willingness to complete GCP training
Experience with IWRS/IRT systems inventory control
Strong organizational and documentation skills with high attention to detail
Proficient in Microsoft Office and electronic data capture systems
Ability to follow protocols SOPs and maintain regulatory compliance
Strong communication and interpersonal skills
Demonstrated ability to manage multiple tasks efficiently and work independently or as part of a team
Professionalism reliability and commitment to patient safety and data integrity
Experience with investigational product handling preferred
Familiarity with Phase IIV clinical trials and regulatory requirements an asset
Experience in a clinical research or hospital setting preferred

Headlands Research will never ask a candidate for personal identifiable information (date of birth social security number drivers license information etc) via email or messenger tools or for a financial deposit of any kind.

Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race color religion age sex national origin disability status genetic information protected veteran status sexual orientation gender identity or expression or any other characteristic protected by federal state or local laws.

Need Assistance

Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process contact for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Required Experience:

Location: Myrtle Beach SC Site Name: Trial Management Associates Full-Time Clinical Research

What We Offer

Competitive pay annual performance incentives
Medical dental and vision insurance
401(k) plan with company match
Paid time off (PTO) and company holidays
A mission-driven culture focused on advancing medicine and improving patient outcomes

Why Join Us

Core Responsibilities:

Investigational Product (IP) Management
- Receive store prepare and dispense investigational products according to protocol pharmacy manual and regulatory requirements.
- Use IWRS/IRT systems to log shipments assign IP and perform returns or destructions per study-specific guidance.
- Maintain accurate inventory logs temperature records and expiration tracking for all IP and supplies.
- Monitor and respond to temperature excursions discrepancies or deviations per SOP.
- Perform aseptic preparations where required following sterile technique protocols.
- Manage IP accountability documentation including blinded and unblinded logs and reconciliation.
- Ensure all investigational product storage complies with GCP and institutional policies (double-locked secure labeled etc.).
Documentation & Compliance
- Maintain audit-ready records of all pharmacy activities including temperature logs equipment calibrations and IP logs.
- Create and manage pharmacy study binders with updated regulatory and protocol-specific content.
- Adhere to ALCOA-C principles (Attributable Legible Contemporaneous Original Accurate Complete and Consistent) in documentation practices.
- Participate in unblinded or blinded monitoring visits providing relevant pharmacy documentation.
Administrative & Operational Support
- Assist with scheduling and performing protocol-specific assessments (e.g. memory assessments vital signs specimen collection support).
- Perform data entry in eCRFs according to protocol and system-specific guidelines.
- Support query resolution documentation scanning and other clerical duties (e.g. faxing reminder calls).
- Order pharmacy-related supplies and assist with equipment upkeep and calibrations.
- Provide pharmacy support to other team members and backfill duties during absences.
Communication & Collaboration
- Maintain clear professional communication with study coordinators monitors sponsors and clinical staff.
- Participate in team meetings and training sessions to stay updated on protocols SOPs and compliance standards.
- Demonstrate flexibility and professionalism in a fast-paced regulated environment.

Requirements:

Minimum of 12 years of experience as a Pharmacy Technician or Medical Assistant required
Completion of a recognized Pharmacy Technician or Medical Assistant program
Registration with relevant state or provincial licensing body (e.g. College of Pharmacists of BC for Pharm Techs for example) required where applicable.
Current certification in Good Clinical Practice (GCP) and/or willingness to complete GCP training
Experience with IWRS/IRT systems inventory control
Strong organizational and documentation skills with high attention to detail
Proficient in Microsoft Office and electronic data capture systems
Ability to follow protocols SOPs and maintain regulatory compliance
Strong communication and interpersonal skills
Demonstrated ability to manage multiple tasks efficiently and work independently or as part of a team
Professionalism reliability and commitment to patient safety and data integrity
Experience with investigational product handling preferred
Familiarity with Phase IIV clinical trials and regulatory requirements an asset
Experience in a clinical research or hospital setting preferred