Study Supervisor
Altasciences
Summary
A Study Supervisor supervises studies, procedures and research assignments; coordinates duties of personnel and study teams; assists with sample and data collection for research studies.
Job description
About The Role
A Study Supervisor supervises studies, procedures and research assignments; coordinates duties of personnel and study teams; assists with sample and data collection for research studies.
What You'll Do Here
- Ensures that assigned studies have appropriately trained staff, necessary supplies, and necessary forms or electronic systems for data collection.
- Performs and trains staff on technical procedures on animals, including; injections, blood draws, collection of urine samples, catheterization, surgical preparation, restraining, anesthesia, tissue collection, animal disposal.
- Monitors progress of studies during the In-Life phases to verify adherence to study guidelines and timelines.
- Attends and participates in meetings regarding study planning.
- Creates, reviews, and revises Standard Operating Procedures (SOP) relating to animals, technical procedures and facility issues.
- Monitors and reports changes in animal behavior or health, and problems with animal room.
- Monitors and maintains animals and facilities in accordance with applicable laws and regulations.
- Monitors and reports problems with data collection or equipment. Sets up equipment for studies.
- Records and enters raw study data into templates for use by Study Directors.
- Operates and maintains selected laboratory equipment. Ensures equipment is GLP compliant.
- Maintains general organization and cleanliness of work area, including; cleaning and disinfecting procedure rooms and preparation areas.
- Provides technical knowledge to training team in developing training manuals and guidelines.
- Ensure animals are housed in accordance with federal and established guidelines.
- Ensures study conduct as described in Protocol. (e.g., dosing, treatments, surgery schedule, necropsy schedule).
- Documents study procedures and results in study notebooks in accordance with Good Laboratory Practices (GLP) regulations (e.g., animal assignment records, anesthesia records, treatment sheets, study events summaries, euthanasia records, necropsy records).
- Performs QC review study and facility data in a timely manner.
- Completes daily research data (e.g., Protocols, schedules for projects).
- Assigns and oversees duties to personnel necessary to complete daily schedules.
- Schedules and assigns appropriate animal species for studies in consultation with the Study Scientist or Study Director. Schedules animal and procedure rooms, and surgery suites.
- Reports information regarding clinical problems with the animals, data collection or equipment to project scientists.
What You'll Need to Succeed
- Bachelor's degree and a minimum of 2 years of related experience
- LATG certification is preferred
- Ability to read and interpret technical documents and industry specific manuals.
- Ability to write advanced reports and correspondence.
- Excellent verbal and written communication skills.
- Well developed interpersonal skills are required.
- Personal/professional integrity and proven discretion in handling confidential information.
- Ability to develop strong trusting relationships in order to gain support and achieve results.
- Capable of managing multiple conflicting priorities.
- Must be self-directed, motivated, and have a willingness to take the initiative to identify and anticipate client needs and make recommendations for implementation.
- Relevant industry experience is a plus.
Requirements
- Bachelor's degree
- Minimum of 2 years of related experience
- LATG certification preferred
- Ability to read and interpret technical documents and industry specific manuals
- Ability to write advanced reports and correspondence
- Excellent verbal and written communication skills
- Well developed interpersonal skills
- Personal/professional integrity and proven discretion in handling confidential information
- Ability to develop strong trusting relationships
- Capable of managing multiple conflicting priorities
- Self-directed, motivated, and willing to take initiative
- Relevant industry experience is a plus
Benefits
- Health Insurance
- Dental Insurance
- Vision Insurance
- 401(k) Matching
- Paid Vacation
- Paid Holidays
- Free Employee Parking
- Free Lunch
- Paid Sick Leave
- Bereavement Leave
- Employee Assistance Program
- Telehealth Programs
- Training & Development Programs
- Employee Referral Bonus
Company overview
Altasciences is a forward-thinking, mid-size contract research organization (CRO) and contract development manufacturing organization (CDMO) that provides integrated, full-service solutions for early phase drug development. Founded in 1992 and owned by Novo Holdings A/S, the company offers pharmaceutical and biotechnology companies a proven, flexible approach to preclinical and clinical pharmacology studies. Their comprehensive services include preclinical safety testing, clinical pharmacology and proof of concept studies, bioanalysis, formulation development, manufacturing and analytical services, program management, medical writing, biostatistics, and data management. With over 1,800 employees across eight facilities in the U.S. and Canada, Altasciences has established itself as a trusted partner for drug development from lead candidate selection through clinical proof of concept and beyond. The company's integrated CRO/CDMO model enables seamless transitions between development phases, reducing complexities, mitigating risks, and accelerating timelines for clients ranging from startups to global pharmaceutical leaders.