Job Title: Clinical Medical Assistant needed in Lincoln NE! This is an URGENT need and will move quickly! Monday to Friday 730 - 430pm CST ! Job DescriptionAssist the Clinical Operations Team in a multifunctional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities.Responsibilities+ Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and SOPs.+ Perform venipuncture, capillary puncture, and/or other fluid collection within the scope of the protocol and local law and regulations.+ With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc.) within the scope of the protocol, local law, and regulations.+ Process, package, and ship laboratory specimens as required per protocol and IATA regulations, if applicable.+ Track, order, and maintain inventory of all laboratory and study-related supplies throughout the course of the clinical trial.+ Enter source data into the sponsor's and/or vendor’s data portal and resolve basic queries in a timely manner under the direction of the Clinical Research Coordinator.+ Communicate with coworkers, leadership, study subjects, sponsors, CROs, and vendors under the direction of the Clinical Research Team.+ Understand good documentation practices when collecting, transferring data to sponsor/CRO data capture systems, and resolving queries under the direction of the Clinical Research Coordinator.+ Understand the informed consent process with an emphasis on ensuring initial and ongoing consent of study subjects.+ Understand basic elements of regulatory documentation required to initiate, maintain, and close a clinical research trial.+ Understand and participate in patient recruiting tasks including but not limited to prescreening potential subjects for clinical research trials either via phone or in person.+ Maintain confidentiality of patient protected health information, sponsor confidential information, and confidential information.+ Ability to escalate potential patient safety issues such as adverse events, serious adverse events, and adverse events of special interest to the Clinical Research Team.+ Clean, organize, and disinfect the patient care, lab, and lab equipment areas as needed.+ Prepare source document charts, copy and/or file medical records and study-related documents as required.+ Perform front office duties as needed including but not limited to answering phones, scheduling subjects, making reminder calls, and updating patient tracking systems.Additional Skills & Qualifications+ High School Graduate and/or technical degree with a minimum of 1 year of relevant experience in the life sciences industry.+ Phlebotomy certification, if applicable.About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:+ Hiring diverse talent+ Maintaining an inclusive environment through persistent self-reflection+ Building a culture of care, engagement, and recognition with clear outcomes+ Ensuring growth opportunities for our peopleThe company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email (% ) for other accommodation options.