105 Athletic Therapy Specialist jobs in the United States

Seeking Compassionate Travel Mental Health Therapy Aide for SUNY Upstate Medical University!

We are committed to connecting passionate Mental Health Therapy Aides with opportunities that align with their personal and professional goals. Our team builds lasting relationships with each provider to understand their unique needs, ensuring placement in roles that support both career growth and lifestyle preferences.

With a dedicated recruiting team focused on your success, we ensure you a role and schedule that truly works for you. We streamline the process with quick interviews and efficient remote onboarding, so you can step into the right position smoothly. If you’re looking for a team that values your well-being and supports you every step of the way, we’d love to have you on board and make an impact in patient care.

Pay Rate: $30/hr

*Rate includes $202 daily tax-exempt stipend

Responsibilities:

· Responsible in a support role for the care and treatment of psychiatric patients under the direction of a Registered Nurse.

· Functions as a participating member of the multi-disciplinary treatment team and assists in the implementation of treatment plans.

Requirements:

· Graduated from high school or have earned a high school equivalency diploma

Seeking Compassionate Travel Mental Health Therapy Aide for SUNY Upstate Medical University!

We are committed to connecting passionate Mental Health Therapy Aides with opportunities that align with their personal and professional goals. Our team builds lasting relationships with each provider to understand their unique needs, ensuring placement in roles that support both career growth and lifestyle preferences.

With a dedicated recruiting team focused on your success, we ensure you a role and schedule that truly works for you. We streamline the process with quick interviews and efficient remote onboarding, so you can step into the right position smoothly. If you’re looking for a team that values your well-being and supports you every step of the way, we’d love to have you on board and make an impact in patient care.

Pay Rate: $30/hr

*Rate includes $202 daily tax-exempt stipend

Responsibilities:

· Responsible in a support role for the care and treatment of psychiatric patients under the direction of a Registered Nurse.

· Functions as a participating member of the multi-disciplinary treatment team and assists in the implementation of treatment plans.

Requirements:

· Graduated from high school or have earned a high school equivalency diploma

Job Requirements: Are you stuck in your current industry and afraid to make a change? Dont underestimate the value you could offer to healthcare. If you enjoy helping others and enjoy improving the experience for patients, then dont be shy and apply. We have the next big career opportunity for you that provides growth. Join our team, you bring the smile well bring the training.

About Bone & Joint: Bone and Joint has one of the most comprehensive teams of orthopedic, pain management, podiatric, physical and occupational therapy experts in Northcentral Wisconsin. We arent a division of another corporate healthcare organization; Bone & Joint belongs to us and we have numerous locations throughout Central Wisconsin. Our mission is to be the best place for patients to receive care, the best place for employees to work, and the best place for physicians to practice medicine.

A Day in the Life of a Registration Specialist (Therapy): Working at our front desk will give you the opportunity to do various tasks. Its a mix of customer service, scheduling, insurance verifications and patient interactions all rolled into one awesome job. Dont fear the unknown, our training is excellent, and we will get you up to speed in no time. Primarily, youll be engaging with and talking to patients over the phone or in person. You can expect to answer their questions, schedule, and check them in for appointments, verify insurance, and work closely with the therapists to ensure proper scheduling.

Qualifications for a Registration Specialist (Therapy): High school diploma or equivalent. Patience, kindness, and the ability to work with people at all levels (internal and external) combined with compassion for our patients. Ability to work in conjunction with staff in a supportive way to troubleshoot and resolve issues. Possess strong customer service skills/interpersonal interactions; ability to handle difficult and angry people constructively. Excellent verbal and written communication, persuasion, relationship building, resolving conflict and integrity.

Work Schedule: To be submitted with requisition.

Ready to Join Our Team? If you think you have what it takes to do this job, then the next step is to fill out our online application. Dont worry, the application is pretty simple as it asks for your resume and to answer some questions to help us get to know you better. We should warn you though, if you are selected to move forward in the hiring process, we will require that you provide us with further details to help us further understand your interest.

Job Summary:

Provides mental health assessment, diagnosis, treatment and crisis intervention services for adult and/or child members who present themselves from psychiatric evaluation with a broad range of mental health needs. Collaborates with treating physician, psychiatric and allied health professional team to plan and direct each individual member treatment program.

Essential Responsibilities:

• Develops, implements, coordinates, and evaluates clinical treatment programs for the diagnosis, treatment, and/or referral of Health Plan members with acute or chronic mental illness. Participates in staff conferences to select, plan, and evaluate treatment programs. Provides outpatient psychotherapy to individuals, couples, families and groups.


• Instructs and counsels patients and their families regarding compliance with prescribed therapeutic regimens and adherence to prescribed medication regimens, within the scope of practice. May administer specialized therapeutic procedures, as appropriate. Provides appropriate support to members family. May develop and conducts psychoeducational classes and groups.


• Prepares intake summaries, treatment plans, and case summaries and maintains ongoing confidential records. Charts members treatment and progress in accord with state and NCQA regulations and in keeping with accepted community standards. May be required to participate in the department on-call rotation.


• Collaborates with physicians in screening and evaluating patients for psychotropic medications, within the scope of practice. Utilizes resources of public and private agencies and community organizations to meet the needs of the members treatment. May develop, implements, and evaluates behavioral medicine and health psychology programs in a variety of settings, including primary care. Provides consultation to other care providers and health educators on matters relating to mental health, health psychology and behavioral medicine.


• May supervise Post Masters Fellows, Associate Clinical Social Workers, Associate Marriage Family Therapists or Associate Professional Clinical Counselors as needed if supervision course is completed.


• May provide appropriate support to members family, including explanation of treatment, instructions in how to support treatment and interventions to increase acceptance of and adherence to treatment, at members request.


• Utilizes resources of public and private agencies and community organizations to meet the needs of the members treatment to include referral of the member and/or members family to external resources, as appropriate. Participates in departmental program development, implementation and evaluation.


• Reports safety concerns to mandated reporting agencies.

Basic Qualifications:

Experience

• N/A

Education

• Masters degree in Social Work, Social Welfare from a clinical track, Clinical or Counseling Psychology or related field required from an accredited college or university.

License, Certification, Registration

• Licensed Clinical Social Worker (California)

• Licensed Marriage and Family Therapist (California)

• Licensed Professional Clinical Counselor (California) AND Licensed Professional Clinical Counselor Couples and Families Endorsement (California) within 24 months of hire

• National Provider Identifier required at hire

Additional Requirements:

• Must be familiar with DSM-V as a means of diagnosis.
• Has experience in assessing, diagnosing and treating a broad range of psychiatric conditions.
• Excellent interpersonal and communication skills.
• Knowledge of social service agencies, state regulations, and professional board standards as is related to member treatment, patient rights, and member/patient confidentiality.
• May be required to participate in the department on-call rotation.
• Knowledge of Evidence-Based Practice and psychotherapy research methods.
• Knowledge of the bio-psycho-social functions that contribute to mental health.
• Accuracy in diagnosing patients and developing effective treatment plans.
• Competence in individual, family and group psychotherapy.
• Professional maturity and ethical integrity necessary for assuming professional responsibilities.
• Commitment to quality of service, teamwork, and participation in a highly interactive multidisciplinary clinic.
• Ability to complete multiple tasks/objectives in a timely manner.
• Must be able to work in a Labor/Management Partnership environment.

Preferred Qualifications:

• Previous post license, experience as a member of a psychiatric treatment team in an outpatient or inpatient setting/program under licensed supervision.
• Previous clinical responsibility to include crisis intervention, individual and group psychotherapy.
• Demonstrated professional maturity and ethical integrity necessary for assuming professional responsibilities, preferred.
• Demonstrated commitment to quality of service, teamwork, and participation in a highly interactive multidisciplinary clinic, preferred.
• Demonstrated ability to complete multiple tasks/objectives in a timely manner, preferred.
• Accuracy in diagnosing patients and developing effective treatment plans, preferred.
• Competence in individual, family and group psychotherapy, preferred.

Job Title: Cell Therapy SpecialistJob Description

Join a pioneering team dedicated to reimagining cell therapies with transformative technologies, offering new treatment options for patients with autoimmune diseases. Contribute to the complex manufacturing of cutting-edge cell therapy products, and be part of the journey towards developing potent yet safer therapies.

Responsibilities

• Execute manufacturing batch records and standard operating procedures (SOPs) for production of clinical material as part of a team in a GMP environment.

• Provide expert consultation on tech transfer activities to the MSAT department.

• Maintain a detailed understanding of the manufacturing process and the equipment used for production of clinical material.

• Assess and resolve common problems during cell therapy product manufacturing.

• Comply with cGMP standards and good documentation practices; timely review executed manufacturing documentation and support internal site audits for compliance.

• Undergo advanced training in required SOPs and work instructions for cell therapy manufacturing; train others when necessary.

• Author and revise SOPs as necessary for cell therapy manufacturing.

• Document Deviations and CAPAs, investigate and resolve problems, identify root cause, and propose process improvements through clear communication to senior leadership.

• Ensure that all supplies for manufacturing are replenished and prepared for use in the clean room environment.

• Assist management with ensuring a steady supply of materials by actively searching for alternative products and suppliers.

Essential Skills

• Cell culture

• Aseptic processing

• Cell therapy or biologics manufacturing

• GMP production

• Excellent documentation skills with a focus on cGMP manufacturing

Additional Skills & Qualifications

• BS Degree in Life Sciences or Engineering

• 2+ years' experience in cGMP production of biologics, preferably with cell therapy experience

• Significant knowledge in biologics manufacturing process, cell culture, and/or cell therapy production

• Ability to apply critical thinking, independent decision-making, high attention to detail, and troubleshooting skills to complex manufacturing issues

• Sterile gowning and aseptic processing qualifications in previous positions

Work Environment

This position involves hands-on work setting up and operating complex equipment in a cleanroom environment. Safety, environmental, and health concerns demand constant attention, requiring strict adherence to company policies, rules, and regulations. The role involves handling biological materials, necessitating the use of personal protective equipment, including eye protection, mask, coverall gown, gloves, and shoe covers. The position requires extended periods of standing in a clean room, up to 3-6 hours at a time, the ability to lift 30 lbs., and occasional weekend and holiday work.

Pay and Benefits

The pay range for this position is $31.25 - $43.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Frederick,MD.

Application Deadline

This position is anticipated to close on Aug 26, 2025.

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.

The 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 due to a disability, please email (% ) for other accommodation options.

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by Takeda Development Center Americas, Inc. for the following job opportunity:

JOB LOCATION: Cambridge, MA

POSITION : Cell Therapy Specialist

POSITION DESCRIPTION: Takeda Development Center Americas, Inc. is seeking a Cell Therapy Specialist with the following duties: Execute unit operations for manufacturing of patient therapies according to standard operating procedures and cGMP, regulatory and safety requirements which includes basic cell culture as well as specialized techniques for cell selection, activation, transduction, and purification; perform operations in a cleanroom environment, using proper controls to assure aseptic processing includes gowning, cleaning, and isolation procedure; perform supporting operations as needed including preparation of consumables, media blending, cleaning, and environmental monitoring; complete manufacturing tasks following standard operating procedures and batch document instructions, completing forms, reports, logs and records of equipment, and batches as required; ensure all training assignments are complete and up to date, to maintain necessary technical skills and knowledge; ensure processing equipment and required materials are available, maintained, and qualified as required for the different manufacturing activities; support investigations in manufacturing and technical deviations; participate in problem identification, problem solving, and change initiatives in cooperation with other teams and function.; up to 20% remote work allowed.

REQUIREMENTS: Bachelor's degree in Biology, Engineering, Biomedical Engineering, or related field plus 1 year of related experience. Prior experience must include: Develop GMP compliant documents such as batch records and procedures for use in a manufacturing setting; Process and culture mammalian cells in a lab environment; Prepare materials for and perform analytical methods in support of clinical manufacturing; Execute GMP activities in support of clinical manufacturing; Media preparation/reagent prep (media/interleukins).

Full time. $80,000 to $130,000 per year. Competitive compensation and benefits.

Qualified applicants can apply at . Please reference job # R0151592 . EOE

Any individual may provide documentary evidence bearing on this application, with information on available workers and information on wages and working conditions, to the Certifying Officer, U.S. Department of Labor, Employment and Training Administration, Office of Foreign Labor Certification, 200 Constitution Avenue, NW, Room N-5311, Washington, DC 20210.

Locations

Boston, MA

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by Takeda Development Center Americas, Inc. for the following job opportunity:

JOB LOCATION: Cambridge, MA

POSITION : Cell Therapy Specialist

POSITION DESCRIPTION: Takeda Development Center Americas, Inc. is seeking a Cell Therapy Specialist with the following duties: Execute unit operations for manufacturing of patient therapies according to standard operating procedures and cGMP, regulatory and safety requirements which includes basic cell culture as well as specialized techniques for cell selection, activation, transduction, and purification; perform operations in a cleanroom environment, using proper controls to assure aseptic processing includes gowning, cleaning, and isolation procedure; perform supporting operations as needed including preparation of consumables, media blending, cleaning, and environmental monitoring; complete manufacturing tasks following standard operating procedures and batch document instructions, completing forms, reports, logs and records of equipment, and batches as required; ensure all training assignments are complete and up to date, to maintain necessary technical skills and knowledge; ensure processing equipment and required materials are available, maintained, and qualified as required for the different manufacturing activities; support investigations in manufacturing and technical deviations; participate in problem identification, problem solving, and change initiatives in cooperation with other teams and function.; up to 20% remote work allowed.

REQUIREMENTS: Bachelor’s degree in Biology, Engineering, Biomedical Engineering, or related field plus 1 year of related experience. Prior experience must include: Develop GMP compliant documents such as batch records and procedures for use in a manufacturing setting; Process and culture mammalian cells in a lab environment; Prepare materials for and perform analytical methods in support of clinical manufacturing; Execute GMP activities in support of clinical manufacturing; Media preparation/reagent prep (media/interleukins).

Full time. $80,000 to $130,000 per year. Competitive compensation and benefits.

Qualified applicants can apply at Please reference job # R0151592 . EOE

Any individual may provide documentary evidence bearing on this application, with information on available workers and information on wages and working conditions, to the Certifying Officer, U.S. Department of Labor, Employment and Training Administration, Office of Foreign Labor Certification, 200 Constitution Avenue, NW, Room N-5311, Washington, DC 20210.