Job Results
Life Sciences
Posted 1 week
Weekend PRN Psychiatrist | Adult and Dual Diagnosis | 1099 | Jacksonville, FL
Wekiva Springs Center - Jacksonville, FL 32216
Opportunity Details: Position Title: Weekend PRN Inpatient General Psychiatrist Location: Jacksonville, FL Wekiva Springs Center, a leading behavioral health hospital located in Jacksonville, Florida, is seeking a Board-Certified or Board-Eligible Psychiatrist to join our Inpatient Adult and Dual Diagnosis programs. This is an excellent opportunity to work with a diverse patient population in a collaborative and supportive environment focused on mental health and addiction recovery. Position Overview: Employment Type: Hospital Employed Weekend PRN Schedule / Hours: PRN Weekends, holidays and vacation coverage Call: after hour tele-phonic call Friday evening through Monday morning Patient Volume: Will vary Practice Setting: Inpatient adult and dual diagnosis Support / Care Team: Multidisciplinary with BH Techs, BH RN, Psychiatric NPs, Social Workers and Therapists Responsibilities: Saturday and Sunday require on-site presence The role primarily involves conducting initial psychiatric evaluations, with follow-up visits and discharges. Tele-phonic overnight call for Weekends (5:00 PM – 8:00 AM) Collaborating with a multidisciplinary treatment team Compensation: Salary: Fee for service and daily rate for overnight call Malpractice coverage negotiable if needed Qualifications: BE/BC in General Psychiatry, BC preferred Active or eligible FL license Active DEA Comfortable treating all ages About the Organization & Community: Experience life in Jacksonville, FL, a city known for its youthful vibe, 22 miles of sun-kissed beaches, exceptional fishing opportunities, historic neighborhoods, innovative coastal cuisine, and prominent local universities. Jacksonville offers a diverse range of activities that cater to every age and interest, making it a vibrant place to live and work. Join our team at one of the largest networks of freestanding behavioral health facilities in the U.S. Psychiatrists who join UHS benefit from the strength of a Fortune 500 healthcare organization with a nationwide network of acute care hospitals, behavioral health facilities, and outpatient programs. This scale provides unmatched stability, consistent patient volume, and the reassurance of working with a trusted industry leader.
Posted 1 week
Physician-Hematologist Oncologist -Nemours Children’s Health, Jacksonville
Nemours Children's Health - Jacksonville, FL
We are seeking a Board‑certified or Board‑eligible Pediatric Hematology/Oncology Physician with specialized expertise in the clinical care and management of children, adolescents, and young adults. The ideal candidate will bring experience in interdisciplinary collaboration and provide both inpatient and outpatient care within a comprehensive program. Responsibilities may include participation in multidisciplinary clinics, contributions to translational or clinical research efforts, and engagement in education of trainees across medical student, resident, and fellowship levels. Applicants should hold an M.D. or equivalent degree and demonstrate a strong commitment to advancing care and knowledge in the field of Pediatric Hematology/Oncology.
Posted 1 week
Anesthesiologist | Palm Coast, FL | AdventHealth
AdventHealth Palm Coast - Palm Coast, FL 32164
General Anesthesiologist | AdventHealth | Palm Coast, Florida Practice Exceptional Medicine. Live Where Others Vacation. Are you looking for an anesthesia practice that offers clinical variety, a collaborative team, advanced technology, and the lifestyle you’ve been searching for? AdventHealth Medical Group is seeking a Board Certified/Board Eligible General Anesthesiologist to join our growing, hospital-managed anesthesia team serving AdventHealth Palm Coast, AdventHealth Palm Coast Parkway, and Palm Coast ASC. Why You’ll Love This Opportunity Hospital-employed, physician-led anesthesia program Join an experienced, collaborative team of 9 anesthesiologists and 15 CRNAs 95% medical direction / 5% personally performed cases, allowing you to practice at the top of your license while leading a highly skilled anesthesia care team Practice in state-of-the-art operating rooms featuring Da Vinci robotic surgery and Mako robotic orthopedic technology Perform advanced regional anesthesia including interscalene, supraclavicular, femoral, and popliteal blocks Support enhanced recovery (ERAS) protocols within a strong and growing orthopedic program Minimal home beeper call, providing an outstanding work-life balance Diverse and engaging case mix including: General Surgery Orthopedics Gastroenterology Gynecology Plastics Urology Interventional Radiology Compensation & Benefits Highly competitive compensation package Sign-on bonus Comprehensive health, dental, and vision benefits Excellent retirement program CME allowance and paid time off Malpractice coverage Relocation assistance available Practice exceptional medicine. Enjoy an exceptional lifestyle. Why Palm Coast? Nestled between St. Augustine and Daytona Beach, Palm Coast offers the best of Florida’s Atlantic Coast without the crowds. Spend your weekends enjoying: Miles of uncrowded beaches Championship golf courses Boating, kayaking, paddleboarding, and fishing Scenic biking and walking trails Waterfront dining and local restaurants Beautiful neighborhoods with excellent schools Convenient access to Jacksonville, Orlando, and historic St. Augustine Whether you’re raising a family, looking for an active outdoor lifestyle, or simply seeking a slower pace with easy access to world-class amenities, Palm Coast delivers. AdventHealth At AdventHealth, we’re committed to extending the healing ministry of Christ by providing whole-person care to every patient, every day. You’ll join an organization recognized for clinical excellence, innovation, physician collaboration, and a culture that supports your professional growth and personal well-being. Join AdventHealth in Palm Coast and discover a career where your work matters—and your life outside of work does too! What We're Looking For MD or DO Completion of an ACGME-accredited Anesthesiology Residency Board Certified or Board Eligible in Anesthesiology Eligible for unrestricted Florida medical licensure A physician who values teamwork, quality, compassion, and patient-centered care
Posted 1 week
Orthopedic Surgeon | Foot & Ankle | Coastal Florida | Seven Pines Outpatient Clinic
Lyerly Baptist - Jacksonville, FL 32256
About Baptist Health Recognized as a top place to work in health care, Baptist Health cares for more patients in Northeast Florida than any other provider, ranking as “most preferred” for more than 30 years. We’re Jacksonville's only locally governed, faith-based, not-for-profit health system and provide a full spectrum of preventive and specialty care through 200+ locations and six hospitals. Our centers of excellence include Baptist MD Anderson Cancer Center, Baptist Heart Hospital, Baptist Neurological Institute and Wolfson Children's Hospital. This role is responsible for the diagnosis, treatment, and management of patients with musculoskeletal conditions. The role involves performing surgeries to address injuries, deformities, or diseases, as well as providing non-surgical treatment options on the musculoskeletal system of the human body. This position emphasizes patient education, collaboration with other healthcare professionals, and a commitment to providing comprehensive, holistic care. Experience/Education Note: 5 year Orthopedic Residency is required. Education/Degree Required: Doctor of Osteopathic Medicine Or Doctor of Medicine Or Baptist Health, founded in 1955, is North Florida's most comprehensive health care system and the area's only non-profit, mission-driven, locally governed health care provider. Baptist Health has over 200 points of care throughout the Northeast Florida region, including our six award-winning hospitals: Baptist Medical Center Jacksonville, Wolfson Children's Hospital, Baptist Medical Center Beaches, Baptist Medical Center Clay, Baptist Medical Center Nassau and Baptist Medical Center South. The most preferred health care system in the region, Baptist Health also includes 57 primary care offices, as well as home health, behavioral health, pastoral care, rehabilitation services, occupational health and urgent care. Primary Location: Seven Pines
Posted 1 week
Orthopedic Surgeon | Foot & Ankle | Coastal Florida | Seven Pines Outpatient Clinic
Lyerly Baptist - Jacksonville Beach, FL 32250
About Baptist Health Recognized as a top place to work in health care, Baptist Health cares for more patients in Northeast Florida than any other provider, ranking as “most preferred” for more than 30 years. We’re Jacksonville's only locally governed, faith-based, not-for-profit health system and provide a full spectrum of preventive and specialty care through 200+ locations and six hospitals. Our centers of excellence include Baptist MD Anderson Cancer Center, Baptist Heart Hospital, Baptist Neurological Institute and Wolfson Children's Hospital. This role is responsible for the diagnosis, treatment, and management of patients with musculoskeletal conditions. The role involves performing surgeries to address injuries, deformities, or diseases, as well as providing non-surgical treatment options on the musculoskeletal system of the human body. This position emphasizes patient education, collaboration with other healthcare professionals, and a commitment to providing comprehensive, holistic care. Experience/Education Note: 5 year Orthopedic Residency is required. Education/Degree Required: Doctor of Osteopathic Medicine Or Doctor of Medicine Or Baptist Health, founded in 1955, is North Florida's most comprehensive health care system and the area's only non-profit, mission-driven, locally governed health care provider. Baptist Health has over 200 points of care throughout the Northeast Florida region, including our six award-winning hospitals: Baptist Medical Center Jacksonville, Wolfson Children's Hospital, Baptist Medical Center Beaches, Baptist Medical Center Clay, Baptist Medical Center Nassau and Baptist Medical Center South. The most preferred health care system in the region, Baptist Health also includes 57 primary care offices, as well as home health, behavioral health, pastoral care, rehabilitation services, occupational health and urgent care. Primary Location: Seven Pines
Posted 1 week
Research Assistant
Flourish Research - Jacksonville, FL
About Us Flourish Research is where clinical trials thrive. Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU! Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. About the Job: We are actively hiring a Research Assistant to support our Jacksonville, FL site. Shift: Monday-Friday regular business hours Location: Onsite FLSA Classification: Non-Exempt Compensation: $18.00 to $24.00 per hour (based on experience) Essential Job Functions: Support CRCs and site staff with protocol-specified patient visits and procedures, which may include, but not limited to, phlebotomy, IVs, injections, vital signs, ECG/EKG, etc. Document assessments and study data per regs/GCP Obtain and document informed consent following federal regulations and IRB guidelines Support patient recruitment efforts and scheduling to meet enrollment goals Maintain accurate source documentation and complete case report forms (CRFs) Report adverse events to supervisors or investigators as needed Help manage study supplies, lab kits, and other trial materials Maintain confidentiality and follow all applicable compliance and ethical standards Communicate effectively with research team members and document relevant study communications Represent Flourish Research professionally in all interactions Perform additional duties as assigned by management Physical Requirements And/or Environmental Factors: Role may require flexible hours to support clinical schedules and site leadership. Daily computer use. Ability to sit or stand at computer for extended periods of time. Ability to drive and daily availability of an automobile. Requirements Bachelor's degree preferred, but not required Clinical research experience is required, and oncology clinical research experience is preferred Minimum of two years of clinical research experience Clinical skills preferred: vital signs, EKG/ECG, phlebotomy, and injections Familiar with e-source reporting via an electronic platform A clear understanding of ICH, FDA, and GCP regulations Impeccable organizational skills and attention to detail Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven High-level critical thinking skills Working knowledge of medical terminology and lab collection/processing/storage procedures Proficiency with computers and Microsoft Office Suite. Benefits Flourish Research offers an excellent comprehensive benefits package to include: Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, employee referral program, employee assistance program, life insurance, disability insurance, and a generous PTO plan covering vacation, sick, personal days and 8 paid holidays. Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.
Posted 1 week
Clinical Research Coordinator
Flourish Research - Jacksonville, FL
About Us Flourish Research is where clinical trials thrive. Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU! Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. About the Job: We are actively hiring a Clinical Research Coordinator to support our Jacksonville, FL site. Shift: Monday-Friday normal work hours Location: Onsite FLSA Classification: Non-Exempt Compensation: $27.00 to $36.00 per hour (depending on experience) ESSENTIAL JOB FUNCTIONS: Execute protocol-specified patient visits and procedures, which may include, but not limited to, phlebotomy, IVs, injections, vital signs, ECG/EKG, etc. Document assessments and study data per regs/GCP; maintain complete source; accurately complete CRFs/eCRFs. Obtain informed consent per federal regs, GCP, and IRB requirements. Ethically recruit qualified subjects to meet enrollment timelines. Complete required/ongoing training; attend investigator meetings/courses; stay current with changing regulations and Flourish policies. Schedule and conduct visits per protocol timelines. Protect confidentiality per HIPAA and all confidentiality agreements. Report AEs promptly; report SAEs to sponsor within 24 hours and notify PI/Sub-I/supervisor. Account for and ensure availability of trial materials (study drug, labs, CRFs, supplies). Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol and policy. Perform duties safely, and in a time-/cost-effective manner compliant with Flourish policies. Represent Flourish professionally in all interactions. Additional duties as assigned by management. Requirements Bachelor's degree preferred, but not required Must have oncology clinical research experience Minimum of two years of clinical research experience Clinical skills highly preferred: vital signs, EKG/ECG, phlebotomy, and injections Familiar with e-source reporting via an electronic platform A clear understanding of ICH, FDA, and GCP regulations Impeccable organizational skills and attention to detail Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven High-level critical thinking skills Working knowledge of medical terminology and lab collection/processing/storage procedures Proficiency with computers and Microsoft Office Suite Flourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others! Benefits Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, employee referral program, employee assistance program, life insurance, disability insurance, and a generous PTO plan covering vacation, sick, personal days and 8 paid holidays. Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.
Posted 1 week
Clinical Research Coordinator
Cancer Specialists of North Florida - Jacksonville, FL 32256
Cancer Specialists of North Florida is recruiting a Clinical Research Coordinator for our busy Specialty Practice. This position will travel outside of their home clinic when needed for coverage. The Clinical Research Coordinator (CRC) will facilitate timely coordination of daily clinical trial activities across multiple research projects and ensure trial protocol compliance. The CRC is responsible for recruitment, screening, consenting, enrollment, and clinical documentation of patients in clinical trials as well as ensuring protocol compliance. The CRC will provide education to patients and staff about trial concepts and requirements for participation. The CRC will work collaboratively with the clinical site, sponsor(s), clinical research organization(s) (CROs), institutional review boards (IRBs), and study participants to ensure execution of the clinical trial in accordance with the trial protocol, Food and Drug Administration (FDA), Good Clinical Practice (GCP) guidelines, and applicable state and local regulations. In addition to this, the CRC assists the research team, physicians and manager with any additional projects requested. Essential duties and responsibilities include the following: Review and develop a familiarity with trial protocol including but not limited to study proceedings and timelines, inclusion and exclusion criteria, confidentiality, and privacy protection Serve as a resource and “expert” for clinical staff and patients regarding clinical trial questions Ensure compliance with research protocols by providing ongoing quality control audits Provides CRC coverage to all CSNF clinics as assigned by manager or team lead. Strong interpersonal and communication skills to effectively collaborate with clinic site staff and research staff. Recruit and screen potential study participants and perform intake assessments for assigned clinical trials in accordance with trial protocol Obtain informed consent in accordance to the Code of Federal Regulations (45 CFR part 46) Coordinate all study visits and assist treating physician with completion of trial activities including but not limited to: schedule participant visits, coordinate participant travel and meals, participant dosing and observation, scheduling and other evaluations, adverse event monitoring, vitals collection, and IVRS management Collect, process, and ship specimens Collaborate with the research pharmacist to perform drug accountability, compliance, and dosing Educate clinical staff regarding study drug administration requirements, including required pre-medications, order of administration, monitoring time points, and the need for infusion start/stop times All other duties as assigned. Full Time M-F position Education and Experience: Bachelor’s degree in science or health related field; BSN, PharmD, MD, or PhD preferred 2+ years of work as a clinical research coordinator in an oncology setting Compensation and Benefits: Salary is commensurate with experience and qualifications. Cancer Specialists of North Florida is an "EEO Employer” and “Drug Free Workplace”
Posted 1 week
Entry Level Environmental Scientist
Tetra Tech - Jacksonville, FL
The Opportunity: Tetra Tech is adding a Staff-Level Environmental Scientist with minimum of 2 years’ experience to join our Jacksonville, FL location. Your Role: Provide staff level technical support on environmental characterization and remediation projects for federal, municipal, commercial, and industrial clients. This individual will assist with execution of large, complex environmental investigation and remediation programs under CERCLA, RCRA and other regulatory programs for Federal, State, and private clients. Why Tetra Tech: At Tetra Tech, we are Leading with Science to solve the world’s most complex challenges. Our industry-leading experts in engineering and consulting are committed to driving positive change in communities around the world. For over 50 years, we have been at the forefront of innovation and sustainability. Today we stand as a market leader, offering cutting-edge solutions in water, environment, energy, and international development. Our work has improved more than 625 million lives around the world. Your Impact: Join Tetra Tech to make a real difference. Our work leverages cutting-edge technologies, advanced analytics, and the expertise of world-class scientists and engineers to create meaningful change around the world. Discover your full potential – join us to advance your career while leaving a lasting legacy. Responsibilities: • Perform work in problem solving situations and find solutions to the problems. • Implement and document health and safety protocol and have current 40-hr HAZWOPER Certification. • Competent inspection of sediment management systems and have Stormwater Management Inspector Certification. • Verbally communicate with people and accurately explain site conditions and site situations to project participants and management. • Operate heavy equipment; must have (NCCER Certification) to assist in project operations. • Must have completed U.S. Army Corps of Engineers Construction Quality Management for Contractors Certification to assist in project operations. • Create a work product that is representative of what is required and perform Quality Control and Quality Assurance measures to achieve the required task. • Conduct groundwater, surface water, and/or soil sampling activities. • Prepare various technical deliverables including reports, letters, proposals, tables, and figures. • Conduct activities in line with internal procedures, legislation, and industry standards. • Pursue continuous professional development and maintain a high degree of discipline, knowledge, and awareness. • Work in a safe manner at all times and report all health and safety incidents and concerns. • Additional duties as required. Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. The requirements listed below are representative of the knowledge, skill, and/or ability required: Mandatory Requirements; o Bachelor’s degree in coastal environmental science. o NCCER Certification o 40 hour-HAZWOPER Certification o Stormwater Management Inspector Certification o Basic computer skills (e.g., Microsoft programs like Word, Excel). o A valid U.S.-based Driver’s License in good standing. o Capable of performing fieldwork, which at times can be extensive. Desired experience, knowledge, and skills o Strong oral and written communication skills. • Willingness and ability to travel as needed, approximately 50%. This position requires the candidate to be a U.S. Citizen due to the projects they will be working on. Background Check (if applicable): If this position requires a CAC card, CUI Enclave Access and/or a Security Clearance, a background check will be completed. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. The employee is frequently required to remain in stationary position for long periods of time, traverse, and perform field investigation and remediation activities that could potentially require the following: performing strenuous fieldwork under a variety of site and weather conditions; standing, crouching and sitting to facilitate collecting site information; negotiating difficult terrain for extended periods of time performing field surveys, move and/or transport field equipment and other items weighing up to 40 pounds; and potential exposure to natural hazards (e.g., poison ivy). Must be able to perform and maintain rigorous detailed documentation of field activities. Specific vision abilities required by this job include the ability to observe details at close range, color vision, peripheral vision, depth perception, and ability to adjust focus. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee occasionally works near moving mechanical parts. The noise level in the work environment is usually moderate. The employee will be required to travel via air or land. The employee may be required to conduct site visits and field activities at places and times where exposure to outdoor weather conditions is part of the working environment. The employee may also be required to work in environments where toxic fumes or chemicals are present. Overnight travel may be required in Florida and the southeast United States typically for periods of up to 5 days. Travel for longer periods and other US or international locations are also possible. Language & Communication Skills: The ability to read, interpret, and understand a variety of instructions furnished in written, oral, diagram, or schedule form is required. A mastery of the English language appropriate for both interpretation of written and oral instructions from numerous sources and for explanation of findings is required. The ability to prepare and write detailed site assessments notes and technical reports. Other Skills: Instructions: Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. Proficiency with Microsoft office software, Adobe and other desktop software packages as required to prepare the required documents associated with this technical discipline. Life at Tetra Tech: The perks of working at Tetra Tech include: • Comprehensive and market-competitive benefits. • Merit-based financial rewards. • Flexibility and company-wide commitment to work/life balance. • Collaborative team atmosphere that values the contributions of all employees. • Learning and development opportunities for ongoing professional growth. About Tetra Tech: Tetra Tech is the leader in water, environment, and sustainable infrastructure, providing high-end consulting and engineering services for projects worldwide. With 30,000 employees working together, Tetra Tech provides clear solutions to complex problems by Leading with Science® to address the entire water cycle, protect and restore the environment, design sustainable and resilient infrastructure, and support the clean energy transition. Tetra Tech is proud to be an Equal Opportunity Employer. All qualified candidates will be considered without regard to race, color, religion, national origin, age, disability, sex, marital or familial status, status as a protected veteran, or any other characteristic protected by law. Tetra Tech is a VEVRAA federal contractor and we request priority referral of veterans. We invite applications from all interested parties. Explore our open positions at https://www.tetratech.com/careers. Follow us on social media to learn more about our people, culture, and opportunities: LinkedIn: @TetraTechCareers Twitter: @TetraTechJobs Facebook: @TetraTechCareers We thank all applicants for their interest, however, only those candidates selected for interviews will be contacted. Please no phone calls or agencies. Additional Information Organization: 112 EGS
Posted 1 week
Clinical Research Physician – Psychiatrist
Alcanza Clinical Research - Jacksonville, FL 32256
Description Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site. Key Responsibilities Essential Job Duties: Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance Evaluates and assesses participants to ensure only eligible participants enroll into the trials. Participates and engages in successful delivery and retention of study participants. Interacts positively and collaboratively with sponsors, clients and team members. Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs. Actively involved in protocol training for staff. Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues. Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company. Skills, Knowledge and Expertise Minimum Qualifications: MD or DO degree, an active physician license (in good standing) in the state of practice for this role is required. Board certification in Psychiatry is required. Required Skills: Clinical skills and clinical procedures based in area of specialty. Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm). Must possess strong organizational skills, attention to detail, and math proficiency. Well-developed written and verbal communication skills. Bi-lingual (English / Spanish) proficiency is highly preferred. Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, employees, subjects, managers and external customers. Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities. Ability to be professional, respectful of others, self-motivated, and exemplify a strong work ethic. Must possess a high degree of urgency, self-motivation, integrity and dependability. Ability to work independently to identify problems and implement solutions. Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines. Benefits Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire. Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered. About Alcanza Clinical Research Alcanza Clinical Research (“Alcanza”) is a national, collaborative network of clinical research sites, founded on the mission to accelerate the development of new therapies by reducing barriers to clinical research participation for all. We conduct research on dozens of conditions in several therapeutic areas including psychiatry, neurology, dermatology, and infectious disease. Our work is important to the patients who participate, the scientists who develop these new therapies, and the entire medical community. Because all approved medications require clinical trials, the impact of your work is exponential, reaching many thousands of future patients and improving their quality of life. Alcanza is a culturally competent organization. We treat each other with dignity, creating an environment where all individuals feel welcome, heard, and respected for their unique perspectives and aspirations. We put considerable effort into finding exceptional employees who mirror the values most important to us: Inclusive, Impactful, Compassionate, and Determined. Alcanza Clinical Research is an Equal Opportunity Employer that values and respects the importance of a diverse and inclusive workforce. It is the policy of the company to recruit, hire, train and promote persons in all job titles without regard to race, color, religion, sex, age, national origin, marital status, veteran status, disability, sexual orientation, gender identity or expression, genetic information, or any other category protected by law. We recognize that diversity and inclusion is a driving force in the success of our company.