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CTG CLINICAL TRIAL ASSOCIATE in Cambridge, Massachusetts

CLINICAL TRIAL ASSOCIATE

Cambridge, Massachusetts, United States

Science

Jul 29, 2019Post Date

19207440Requisition #

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Computer Task Group is seeking a Clinical Trial Associate for their client in Cambridge, MA for a one year contract.

Effectively and efficiently interact with internal, clinical site and vendor personnel.

Have the interest and ability to expand knowledge of clinical trial management procedures and regulatory submission requirements.

Learn health care authority regulations and guidelines, and apply to daily activities.

Perform day-to-day activities based on Standard Operating Procedures and Good Clinical Practice (GCP).

Learn and execute defined tasks while working closely with others.

Assist with in-house coordination of activities related to conduct of clinical trials.

Demonstrate problem-solving skills, including the identification of problems and proposed solutions, in consultation with more senior team members.

Possess good verbal skills and seek information when needed.

Seek opportunities to learn and be receptive to constructive feedback.

Benefit from close supervision but be willing to work independently.

Receive guidance on clinical development process and the role operations plays in that process.

Track progress across multiple programs and communicate this to internal and external stakeholders.

Organize trial and program related team meetings, associated agendas, and generate meeting minutes, including tracking of action items.

Become familiar with and assist in maintaining clinical invoice tracking and other budget databases for multiple projects, generate periodic reports on status of payments and other database reports, and resolve payment inquiries from investigator sites.

Maintain other informational databases for clinical trial status throughout the life of a clinical program.

Train to monitor clinical sites / data under the direction of experienced clinical research personnel through co-monitoring visits.

Travel as needed, although requirements are minimal (less than 20% for non-monitoring related work; potential at times for up to 50% for monitoring related travel).

Some experience working in a contract research organization and/or clinical trial environment is preferred

Entry level is acceptable

Candidates may apply below or email resumes to roberta.allegrino@ctg.com

CTG (NASDAQ: CTG) provides industry-specific IT services and solutions that address the business needs and challenges of clients in high-growth industries in North America and Western Europe. CTG also provides strategic staffing services for major technology companies and large corporations. Backed by more than 50 years of experience and proprietary methodologies, CTG has a proven track record of reliably delivering high-value, industry-specific staffing services and solutions to its clients. CTG has operations in North America, Western Europe, and India.

CTG's greatest asset is its people, and as such, we are committed to providing employees programs and processes to support their performance, hone their skills, and advance in their careers. This commitment is reflected by CTG being named a Best Places to Work in Healthcare company by Modern Healthcare (2013-2016) in North America, and a Best Workplace in the United Kingdom (2013), Belgium (since 2007), and Luxembourg (since 2011).

CTG will consider for employment all qualified applicants including those with criminal histories in a manner consistent with the requirements of all applicable local, state, and federal laws.

CTG is an Equal Opportunity/Affirmative Action Employer and strong advocate of workforce diversity. Minority/Female/Sexual Orientation/Gender Identity/Disability/Veteran.

Additional Information

  • Job Function: Clinical Trials & Studies

  • Education Level: Associate's Degree/College Diploma (±13 years)

  • Work Remote: No

  • Travel: Yes, 20 % of the Time

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