Clinical Research Associate II/III - US

Location: Remote Who we are? Optimapharm is a

mid-sized, global Contract Research Organisation (CRO) turning science into hope

through agile, patient-focused clinical development. We specialise in Phase I-IV clinical studies, delivering Full-Service and Functional Service Provision (FSP) solutions that help sponsors move faster and execute with confidence. With operations in 40+ countries and 2x the patient reach of the average mid-sized CRO, we enable accelerated regulatory pathways, faster study start-up, and access to diverse patient populations worldwide. At Optimapharm, you'll contribute to meaningful clinical research while growing your career in a dynamic, people-focused, global environment. As we expand our US Clinical Operations team, we're searching for a

CRA II/III

who is motivated by quality, driven by purpose, and eager to contribute to innovative clinical research that changes lives. Joining Optimapharm means more than taking on your next role - it's an opportunity to build a long-term career with a global CRO that values growth, development, and excellence. Our structured career pathway provides clear progression and recognition of your expertise: CRA I → CRA II → CRA III → Senior CRA. Here, your dedication is rewarded with meaningful growth opportunities, exposure to diverse studies, and the support needed to reach your full potential. What do we offer? Working in a successful company that's growing and developing every day Being part of a clinical research team that transforms science into hope for patients International projects and professional growth Company that supports life balance Company with healthy culture Working with a highly experienced team of clinical research professionals Competitive salary Competitive PTO entitlement Health insurance, including vision and dental plans, to meet your and your family's needs Comprehensive pension plan to maximize savings and prepare confidently for the future Employee engagement programs Well-being initiatives Training and development program Fast-paced career path progression Who are we looking for? Qualifications and Experience University degree,

preferably in medical or life sciences;

nursing education or other relevant healthcare college degree At least

2

years

of independent clinical trial monitoring experience High level of knowledge of ICH GCP Guidelines, knowledge of regulatory requirements and a strong interest in clinical research Computer proficiency is mandatory Ability to read, analyze, and interpret common scientific and technical journals Excellent verbal and written communication skills Very good interpersonal and negotiation skills Ability to work independently, pro-active Affinity to work effectively and efficiently in a matrix environment A current, valid driver's license Your

responsibilities Perform routine site visits independently, including pre-study, initiation, interim monitoring and closeout visits Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirements Independently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicable Identifying and escalating potential risks and identifying retraining opportunities for site personnel Preparation of corrective and preventive (CAPA) plans for issues identified during monitoring activities and pro-active follow of each, individual CAPA until timely resolution Preparation of documents required for EC submissions and notifications, translation of study-related documents (where applicable), and other tasks as instructed by the supervisor Independently negotiate study budgets with potential investigators/institutions and assist with the execution of site contracts as applicable Administration of site payments in accordance with relevant project instructions By joining our fast-growing and prosperous team, you will have an excellent opportunity for further personal growth and career development. If you would be interested in joining the Optimapharm team, please

send your CV a

nd note that only shortlisted candidates who meet the requirements will be contacted for the further selection process. Compensation is competitive and final offers will reflect each candidate's experience, skills, and qualifications. Disclaimer

: Unsolicited CVs sent to Optimapharm (Talent Acquisition Team, Hiring Managers or any other OPT employee) by recruitment agencies will not be considered for this role. Optimapharm follows a direct sourcing strategy and collaborates exclusively with selected recruitment partners when external support is required.